LAURYL MYRISTYL ALCOHOL


Lauryl-Myristyl Alcohol
EC / List no.: 279-420-3
CAS no.: 80206-82-2


Lauryl-Myristyl Alcohol is blend of high purity linear primary alcohols with 12-14 carbon chain lengths, based on renewable or petrochemical resources.
Lauryl/Myristyl Alcohol is C12-14 alcohol blend which is a clear to cloudy, colourless liquid. 
High purity alcohol blend Lauryl myristyl alcohol is used to manufacture rheology modifiers, specialty monomers and modifying resins


Alcohols, C12-14
alcohols C12-14
tridecan-1-ol
C1214 Lauryl Myristyl Alcohol
Dodecanol, tetradecanol and hexadecanol
Fatty alcohols
Nafol 1214

Lauryl/Myristyl Alcohol is a process mixture consisting primarily of Lauryl (C12) and Myristyl (C14) alcohols.

Lauryl/Myristyl Alcohol is Saturated fatty alcohol blend and Lauryl/Myristyl Alcohol is chemical intermediate for surfactants and are used in various applications like the production of personal care and home care products, pharmaceutical formulations, agrochemicals and industrial uses.
• Detergents and Cleaners
• Cosmetics and Pharmaceuticals
• Flavour and Fragrances
• Lubricating Oil Additive
• Metal Working
• Textile and Leather Application
• Polymer Auxiliaries


Lauryl Alcohol (and) Myristyl Alcohol.

Lauryl-Myristyl Alcohol is used in many cosmetic and skin care products. Lauryl myristyl alcohol provides emollient effect, lubricity and emulsion stabilization. 
Lauryl myristyl alcohol acts as a viscosity controller.

Product Group: Fatty Alcohol
Synonym: Dodecanol Tetradecanol
Product Family: Lauryl Myristyl Alcohol
Chain Length: C1214 Alcohol
CAS Number: 67762-41-8

CAS No.: 80206-82-2

Synonyms: Dodecanol Tetradecanol

Lauryl Myristyl Alcohol is used as an intermediate in the manufacture of surfactants.

Lauryl myristyl Alcohol (C1214): Colourless liquid product with typical fatty alcohol odour. Used directly as foam stabilizer, detergency boosting & lubricant additives. 
Major Application in manufacture of Chemical Intermediates, Surfactants and Textile chemicals.

Category: Fatty Alcohols,Lauryl Myristyl Alcohol


Lauryl Myristyl Alcohol is a colorless liquid with a characteristic fatty alcohol odor. 
The principal uses for Lauryl Myristyl Alcohol are as a raw material for surfactants, emulsion stabilizer for creams and lotions, quality modifier of lipsticks and an additive for ointment base and cream conditioners.

Lauryl Myristyl Alcohol (C12-14)
Lauryl Myristyl Alcohol, also known as C12-14 Alcohol, is a fatty alcohol. It’s C1214 chain length allows it to be used in a variety of industries and applications ranging from Industrial and Personal Care to Textile and Household cleaners.

Grade

Industrial
Other Names

Dodecanol
Tetradecanol
Hexadecanol
C12-14
Form

Liquid
Abbreviations

C12-14


Applications: 
Derivatives of the detergent range C12 to C14 alcohols are used in light- and heavy-duty detergents, laundry pre-softeners, hard surface cleaners, disinfectant, cleaners, metal cleaners, textile processing, pulp and paper processing, wastepaper deinking, agricultural uses in pesticides and soil conditioners, and in metalworking as surface lubricants, etc.

Applications: 
Derivatives of the detergent range C12 to C14 alcohols are used in light- and heavy-duty detergents, laundry pre-softeners, hard surface cleaners, disinfectant, cleaners, metal cleaners, textile processing, pulp and paper processing, wastepaper deinking, agricultural uses in pesticides and soil conditioners, and in metalworking as surface lubricants, etc.


Lauryl myristyl alcohol is a type of fatty alcohol which is a form of the combination of C12 and C14 that is lauryl and myristyl. 
Lauryl myristyl alcohol is also known as DodecanolTetradecanol. 

Laurel myristyl alcohol is colorless liquid and has a mild odor and decomposes when subjected to excessive heat. 
The life span of Laurel myristyl alcohol is one year from its date of manufacturing. 
The Lauryl myristyl alcohol has extensive uses in several industries including food, cosmetic, automotive, textile, and chemical industries. 
Moreover, Lauryl Alcohol is used as an intermediate in the manufacture of surfactants.


Global lauryl myristyl market alcohol is driven by rising chemical and manufacturing industries. 
The wide range of application in various industries leads to increase the demand for lauryl myristyl alcohol. 
The consumers are using more of personal care products which further leads to increase in usage lauryl myristyl alcohol in cosmetics. 
Macroeconomic factors such as increasing disposable income, literacy rate, the rapid rate of urbanization, and change in lifestyle also lead to the growth of lauryl myristyl alcohol market. 
The lauryl myristyl alcohol causes corrosive of ingestion, irritation to skin and eye contact, inhalation problem. 
Severe overexposure can cause death leads to restraining the growth of the market.

Name: Alcohols, C12-14
Synonyms: Alfol 1214; Alfol 1412; C12-14 alcohols; CO 1217; CO 1270A; Dyanol; Elocol C 1214; Epal 12/70; Epal 12/85; Epal 1214; Fatty alcs., C12-14; Fine Oxocol 1213; Kalcohl 2474; Kalcohl 6-24; Kalcohl 724A; Kalcol 2470; Lorol 1214S; Lorol 5; Lorol DD; Lorol S; Marlanol 24; Nafol 1214; Nafol 1214S; PY 126; Sipol C12-C14; Tensioactiv CL 9
CAS Registry Number: 80206-82-2
EINECS: 279-420-3


The global Lauryl myristyl alcohol is segmented into seven regions includes North America, Latin America, Asia-Pacific excluding Japan, Eastern Europe, Western Europe, Japan and The Middle East and Africa. 
Asia Pacific is expected to be the fastest growing Lauryl myristyl alcohol regional market. 
Moreover, the Asia Pacific and Japan has shown the growth in Lauryl myristyl alcohol market owing to rise in demand for the food and cosmetic industry in the region. 
European Lauryl myristyl alcohols market is expected to decline share to high growth in areas such as Asia Pacific and Latin America. 
The uncertain economic circumstance in the region combined with declining growth in the main downstream industries is relied upon to have an adversely affect the Lauryl myristyl alcohols market. 
North America Lauryl myristyl alcohols market is foreseen to witness average growth over the anticipated period due to expanding the bio-based product.

Based on uses, the global Lauryl myristyl alcohol market is segmented into:

Surfactants and Easters
Lubricants and Greases
Personal Care
Soaps and Detergents
Metal cleaners
Pulp and Paper Processing


Based on end-use industry, the global Lauryl myristyl alcohol market is segmented into:

Cosmetics Industry
Chemical Industry
Automotive Industry
Textile Industry
Petrochemical Industry
Ceramics industry
Pharmaceuticals Industry
Construction Industry


Based on Product type, the global Lauryl myristyl alcohol market is segmented into:

Additives
Chemicals
Metallic Stearates
Oleochemicals
Pigments
Polymers
PVC Heat Stabilizers
Titanium Dioxide

Final product applications
Agricultural chemicals
Detergents and cleaners
Detergents for household purposes
Flavors and fragrances
Industrial applications
Lubricants
Metal working and fuel additives
Additives
Oil and gas
Paints
Inks
Coatings
Adhesives
Paper chemicals
Water treatment
Paper coating
Personal care
Plastic and rubber additives
Specialty
Textile
Leather processing

Dodecanol /ˈdoʊˈdɛkɑːnɒl/, or lauryl alcohol, is an organic compound produced industrially from palm kernel oil or coconut oil. 
Lauryl alcohol is a fatty alcohol. 
Sulfate esters of lauryl alcohol, especially sodium lauryl sulfate, are very widely used as surfactants. 

Sodium lauryl sulfate, ammonium lauryl sulfate, and sodium laureth sulfate are all used in shampoos. 
Lauryl alcohol is tasteless and colorless with a floral odor

Lauryl Alcohol is an Intermediate, Corrosion Inhibitor in Metal Working Fluids, Chemical Intermediate in Pharmaceuticals, Dispersant in Surfactant Production.

Lauryl alcohol is used in skincare, haircare, and body care formulation products in cosmetics.


CAS 112-53-8  
EINECS 203-982-0 

Lauryl alcohol is an organic compound classified as a fatty alcohol. Lauryl alcohol is a tasteless, colorless solid with a floral smell. 
The substance finds use in synthetic detergents, lube additives, pharmaceuticals, cosmetics, rubber, textiles, perfumes, and as a flavoring agent. 
Lauryl alcohol is also used as a chemical intermediate for the production of n-dodecyl sulfate salts, and in the manufacture of n-dodecyl ethoxylates.

Lauryl Alcohol, also called Dodecanol, is a fatty alcohol obtained from the hydrogenation of palm kernel or coconut oil fatty acids. 
Lauryl Alcohol is used in Arcylates and Methacrylates, and is also an ingredient for producing surfactants and lubricating oils.

Lauryl alcohol, is an organic compound produced industrially from palm kernel oil or coconut oil.

INCI: Lauryl alcohol
What is Lauryl alcohol?
Lauryl alcohol, also known as dodecanol, is an organic fatty alcohol.  
On a large-scale basis, Lauryl alcohol is produced from palm kernel oil or coconut oil. Lauryl alcohol is a tasteless, colorless and floral odor.

Use & Benefits: 
Lauryl alcohol is used vastly in the cosmetic industry in preparation of emulsion. 
When Lauryl alcohol is used in emulsion it can stabilize emulsion by getting incorporated into water and oil phase. 
Lauryl alcohol is fatty in nature, so when it is used on the skin, it also provides fat and moisture to the dried skin. 
Lauryl alcohol forms a layer on the skin which does not allow moisture to evaporate. 
So, when applied on the dried skin it gets a boost of moisture as well. 
Lauryl alcohol can also be used as a viscosity increasing agent. 
Lauryl alcohol is used in skincare, haircare, and body care product.  


INCI Name: Lauryl Alcohol
Lauryl Alcohol is a natural fatty alcohol that acts as a liquid conditioner, spreading agent and coupling agent. Lauryl Alcohol is compatible with anionic and cationic surfactants and is stable over the pH range normally encountered in cosmetics and toiletries.

Key Benefits

Liquid Fatty Alcohol
Spreading and Coupling Agent


Lauryl Alcohol is mainly used as emulsifier and emulsion stabilizer to ensure the oil/ water phase is properly mixed and the emulsion is stable over shelf life of the product. Further it helps to soften the hair and protect it from moisture loss.

Emollient
Emulsifying Agent
Emulsion Stabilising Agent
Viscosity Controlling Agent
Foam Booster
Fragrance Ingredient


Lauryl alcohol is organic tasteless, colourless solid with a floral smell. 
Lauryl alcohol is classified as a fatty alcohol. 
Lauryl alcohol is used to make surfactants, lubricating oils, pharmaceuticals, in the formation of monolithic polymers and as a flavor enhancing food additive,used as an emollient.
Lauryl alcohol is also the precursor to dodecanal, an important fragrance. Lauryl alcohol can be obtained from palm kernel or coconut oil fatty acids and methyl esters by hydrogenation.

Lauryl Alcohol is an emulsifier that can be found in cosmetic products including hair conditioner and body lotions. 
Lauryl Alcohol helps bind ingredients together and keep a formula from separating. 
Over time, it is possible for formulas in a product to separate. 
Formulators add emulsifiers to our products where needed to ensure that our products provide the same performance use after use. 


Lauryl Alcohol is a common load bearing additive used in rolling oil for cold rolling of aluminum. 
Lauryl Alcohol imparts a number of desirable properties to the rolling oil but its primary functions are to insure the uniform thickness of sheets, free from objectionable surface defects is obtained and a smooth functioning of rolling operation

Use & Benefits: 
Lauryl alcohol is used vastly in the cosmetic industry in preparation of emulsion. When it is used in emulsion it can stabilize emulsion by getting incorporated into water and oil phase. It is fatty in nature, so when it is used on the skin, it also provides fat and moisture to the dried skin. It forms a layer on the skin which does not allow moisture to evaporate. So, when applied on the dried skin it gets a boost of moisture as well. It can also be used as a viscosity increasing agent. It is used in skincare, haircare, and body care product.  

Applications: Bath & Shower, Skin Care, Green & Natural, Hair Care, Sun Care, Baby Care
Functions: Emulsion Stabilizer


Production and use

Lauryl alcohol can be obtained from palm kernel or coconut oil fatty acids and methyl esters by hydrogenation.
Lauryl alcohol may also be produced synthetically via the Ziegler process. 
A classic laboratory method involves Bouveault-Blanc reduction of ethyl laurate.

Dodecanol is used to make surfactants, lubricating oils, pharmaceuticals, in the formation of monolithic polymers and as a flavor enhancing food additive. 
In cosmetics, dodecanol is used as an emollient. 
Lauryl alcohol is also the precursor to dodecanal, an important fragrance, and 1-bromododecane, an alkylating agent for improving the lipophilicity of organic molecules.

Lauryl Alcohol
Product description
CAS No.: 112-53-8

Synonyms: Dodecanol, 1-Dodecanol, Dodecyl alcohol, Dodecan-1-ol

ALCOHOL C-12 (LAURYL ALCOHOL)
ALCOHOL C-12 (LAURYL ALCOHOL) 1-DODECANOL/DODECYLIC ALCOHOL/LAURYL ALCOHOL

dodecan-1-ol  has parent hydride dodecane 
dodecan-1-ol has role cosmetic 
dodecan-1-ol has role insect attractant 
dodecan-1-ol has role insecticide 
dodecan-1-ol has role pheromone 
dodecan-1-ol has role plant metabolite 
dodecan-1-ol is a dodecanols 
dodecan-1-ol is a fatty alcohol 
dodecan-1-ol is a primary alcohol 

Lauryl alcohol is used to produce surfactants, lubricant oils and pharmaceuticals.

Pharmaceuticals and Cosmetics use of Lauryl Alcohol : 
Lauryl Alcohol is an emulsion stabilizer for creams and lotions. It is Quality modifier of lipsticks. 
Lauryl Alchol is an Additive for ointment base and cream conditioners. 
Lauryl alcohol acts as the smooth touch to skin for cosmetic uses. It is Auxiliary for emulsifiers and Thickening agent formulations


Lauryl Alcohol is a natural fatty alcohol that acts as a liquid conditioner, spreading agent and coupling agent. 
Lauryl Alcohol is compatible with anionic and cationic surfactants and is stable over the pH range normally encountered in cosmetics and toiletries.

Use: Cosmetics and Personal Care, Cleaning and Detergents, Industrial, Pharmaceutical and Veterinary


Applications
1-Dodecanol is used as a cosmetic, textile auxiliaries, synthetic oil, emulsifiers and flotation agent of raw materials, a detergent raw material, a foaming agent of the toothpaste.

Other names: Dodecyl alcohol; n-Dodecan-1-ol; n-Dodecanol; n-Dodecyl alcohol; Alcohol C-12; Alfol 12; Dodecanol-1; Dytol J-68; Karukoru 20; Lauric Alcohol; Laurinic alcohol; Lauryl alcohol; Lauryl 24; Pisol; S 1298; Sipol L12; Siponol L2; Siponol L5; Siponol 25; 1-Dodecyl Alcohol; Duodecyl alcohol; n-Lauryl alcohol; Dodecan-1-ol; Cachalot l-50; Cachalot l-90; Lorol 11; Lorol 5; Lorol 7; CO-1214; CO-1214N; CO-1214S; Epal 12; n-Lauryl alcohol, primary; MA-1214; Dodecanol; 1-Hydroxydodecane; Hydroxydodecane; Lorol C12; Undecyl carbinol; Adol 10; Adol 12; NAA 42; Nacol 12-96; Hainol 12SS; Conol 20P; Conol 20PP; 1322-35-6; 68855-55-0; 8014-32-2; 8032-08-4; 8032-09-5

LAURYL ALCOHOL is classified as :
Emollient
Emulsifying
Emulsion stabilising
Viscosity controlling
CAS Number    112-53-8
EINECS/ELINCS No:    203-982-0
COSING REF No:    77060
Chem/IUPAC Name:    Dodecan-1-ol


IUPAC Name 
dodecan-1-ol
Synonyms     
1-Dodecanol    
1-Hydroxydodecane    
dodecan-1-ol    
Dodecyl alcohol    
Dodecylalcohol    
Dodecylalcohol    
Lauroyl alcohol    
Lauryl alcohol    
n-Dodecan-1-ol    
n-Lauryl alcohol    
Undecyl carbinol


Preferred IUPAC name: Dodecan-1-ol

Other names
Dodecanol
1-Dodecanol
Dodecyl alcohol
Lauryl alcohol

CAS Number: 112-53-8 


Chemical formula: C12H26O
Molar mass: 186.34
Appearance: Colorless solid
Density: 0.8309
Melting point: 24 °C 
Boiling point: 259 °C 
Solubility in water: 0.004 g/L
Solubility in ethanol and diethyl ether: Soluble
Magnetic susceptibility (χ): -147.70·10−6 cm3/mol


1 Dodecanol
1-Dodecanol
Alcohol, Dodecyl
Alcohol, Lauryl
Alcohol, n-Dodecyl
Dodecanol
Dodecyl Alcohol
Lauryl Alcohol
n Dodecyl Alcohol
n-Dodecyl Alcohol


1-Dodecanol is a saturated 12-carbon fatty alcohol obtained from coconut oil fatty acids. It has a floral odor and is used in detergents, lubricating oils, and pharmaceuticals.


Dodecan-1-ol is a fatty alcohol that is dodecane in which a hydrogen from one of the methyl groups is replaced by a hydroxy group. 

Lauryl alcohol is registered for use in apple and pear orchards as a Lepidopteran pheromone/sex attractant, used to disrupt the mating behaviour of certain moths whose larvae destroy crops. 
Lauryl alcohol has a role as a cosmetic, a pheromone, an insect attractant, a pesticide and a plant metabolite. 
Lauryl alcohol is a primary alcohol, a fatty alcohol and a member of dodecanols. 
Lauryl alcohol derives from a hydride of a dodecane.


Use & Benefits: 
Lauryl alcohol is used vastly in the cosmetic industry in preparation of emulsion. When Lauryl alcohol is used in emulsion it can stabilize emulsion by getting incorporated into water and oil phase. 
Lauryl alcohol is fatty in nature, so when it is used on the skin, it also provides fat and moisture to the dried skin. 
Lauryl alcohol forms a layer on the skin which does not allow moisture to evaporate. 
So, when applied on the dried skin it gets a boost of moisture as well. 
Lauryl alcohol can also be used as a viscosity increasing agent. Lauryl alcohol is used in skincare, haircare, and body care product.  

Large amount Lauryl Alcohol is used as special solvents, fillers in plasticizer and insulating materials for the building industry. 
Lauryl Alcohol is used as ingredient in the industries of agricultural, foodstuff, metal processing, cosmetics, lube additive, pharmaceutical, rubber, textile, perfume and flavouring as well as synthetic detergent.


Dodecanol is a colorless thick liquid with a sweet odor. Floats on water. Freezing point is 75°F.


1-Dodecanol Chemical Properties,Uses,Production
Description
Lauryl alcohol has a characteristic fatty odor. It is unpleasant at high concentrations but delicate and floral on dilution. It has a fatty, waxy flavor. It may be prepared by hydrogenation of lauric acid; normally employed as a replacement for the corresponding aldehyde.

Chemical Properties
Lauryl alcohol has a characteristic fatty odor; unpleasant at high concentrations, but delicate and floral on dilution. It has a fatty, waxy flavor.

Chemical Properties
1-Dodecanol is a crystalline solid that has a melting point of 24°C.
The air odor threshold for dodecyl alcohol (isomer not specified) is reported to be 7.1 ppb.

Chemical Properties
white low melting crystalline solid

Occurrence
Reported found in the oil of Mexican lime and in the oil from flowers of Furcraea gigantean. 
Also reported found in apple, banana, sour cherry, citrus peel oils, melon, pineapple, potato, thymus, cheeses, butter, milk powder, chicken and beef fat, cooked pork, beer, whiskies, white wine, peanuts, beans, mushrooms, mango, coriander seed and leaf, rice, Bourbon vanilla, endive, crab, clam, Cape gooseberry, pawpaw and maté.

Uses
Used as esterification agent.

Uses
1-Dodecanol is used in chemical formulations for a variety of purposes, including as an emulsion stabilizer, a skin-conditioning emollient, and a viscosity-increasing agent.

Definition
ChEBI: A fatty alcohol that is dodecane in which a hydrogen from one of the methyl groups is replaced by a hydroxy group. It is registered for use in apple and pear orchards as a Lepidopteran pheromone/sex attractant, used to disrupt the mating behaviour of certa n moths whose larvae destroy crops.

Production Methods
1-Dodecanol is produced commercially by the oxo process and from ethylene by the Ziegler process, which involves oxidation of trialkylaluminum compounds. It can also be produced by sodium reduction or high-pressure hydrogenation of esters of naturally occurring lauric acid.

Preparation
Commercially prepared by hydrogenation of lauric acid; normally employed as a replacement for the corresponding aldehyde.

General Description
Colorless thick liquid with a sweet odor. Floats on water. Freezing point is 75°F.

Reactivity Profile
Dodecyl alcohol is an alcohol. Flammable and/or toxic gases are generated by the combination of alcohols with alkali metals, nitrides, and strong reducing agents. They react with oxoacids and carboxylic acids to form esters plus water. Oxidizing agents convert them to aldehydes or ketones. Alcohols exhibit both weak acid and weak base behavior. They may initiate the polymerization of isocyanates and epoxides.

Health Hazard
Liquid will cause burning of the eyes and may irritate skin.

Chemical Reactivity
Reactivity with Water No reaction; Reactivity with Common Materials: No reaction; Stability During Transport: Stable; Neutralizing Agents for Acids and Caustics: Not pertinent; Polymerization: Not pertinent; Inhibitor of Polymerization: Not pertinent.

Safety Profile
Moderately toxic by intraperitoneal route. Mildly toxic by ingestion. A severe human skin irritant. Questionable carcinogen with experimental tumorigenic data. Combustible when exposed to heat or flame; can react with oxidizing materials. To fight fire, use dry chemical, CO2. When heated to decomposition it emits acrid smoke and irritating fumes

Carcinogenicity
1-Dodecanol showed weak tumor-promoting activity when applied three times a week for 60 weeks to the skin of mice that had previously received an initiating dose of dimethylbenz[a]anthracene. Papillomas developed in 2 of 30 mice after 39 and 49 weeks of treatment.
Metabolism
See alcohol C-8.

Purification Methods
Crystallise dodecanol from aqueous EtOH, and distil it through a spinning-band column under vacuum.

1-DODECANOL
Dodecan-1-ol
Dodecanol
Dodecyl alcohol
Lauryl alcohol
112-53-8
n-Dodecyl alcohol
Undecyl carbinol
Dodecylalcohol
Lauric alcohol
Laurinic alcohol
1-Dodecyl alcohol
Pisol
n-Dodecan-1-ol
Duodecyl alcohol
1-Hydroxydodecane
Siponol L5
Karukoru 20
Lauroyl alcohol
Siponol 25
Lorol 5
Lorol 7
n-Dodecanol
Lauryl 24
Alcohol C-12
Alfol 12
Lorol 11
Sipol L12
Dytol J-68
Siponol L2
Cachalot L-50
Cachalot L-90
Dodecyl alcoho
Alcohols, C8-18
n-Lauryl alcohol
C12 alcohol
Hainol 12SS
Hydroxydodecane
Conol 20P
Conol 20PP
Lorol
EPAL 12
Adol 10
Adol 12
Dodecanol-1
n-Lauryl alcohol, primary
Nacol 12-96
NAA 42
CO-1214N
CO-1214S
MFCD00004753
Alcohol C12
S 1298
UNII-178A96NLP2
CO-1214
MA-1214
Alcohols, C12-13
Lorol C12
Co-1214S1-dodecanol
68551-07-5
CHEBI:28878
178A96NLP2
27342-88-7
DSSTox_CID_6918
DSSTox_RID_78253
DSSTox_GSID_26918
C8-18 Alcohols
Fatty alcohol(C12)
Adol 11
Lorol C 12
FEMA Number 2617
Dytol J-68 (VAN)
Lorol C 12/98

1DO
CAS-112-53-8
CCRIS 662
Dodecanol, 1-
FEMA No. 2617
HSDB 1075
NSC 3724
EINECS 203-982-0
BRN 1738860
Fatty (C8-C18) alcohol
laurylalcohol
dodecanol group
Lorol special
AI3-00309
Lipocol L
1-dodecanol group
EINECS 271-359-0
Philcohol 1200
CCCCCCCCCCCC[O]
1-Dodecanol, 98%
Lorol C8-C10 special
Lorol C12-C14
1-Dodecanol, 98.0%
EC 203-982-0
SCHEMBL6844
ACMC-1C59L
4-01-00-01844 (Beilstein Handbook Reference)
CHEMBL24722
C12H25OH
WLN: Q12
Lauryl alcohol, >=98%, FG
DTXSID5026918
1-dodecanol (ACD/Name 4.0)
1-Dodecanol, analytical standard
NSC3724
1-Dodecanol, reagent grade, 98%
BCP29203
CS-D1360
HY-Y0289
NSC-3724
ZINC1529403
Tox21_202124
Tox21_300120
ANW-16485
LMFA05000001
SBB008734
STL301829
Co 12Co-1214Co-1214N
AKOS009031450
DB06894
MCULE-9381688904
NE10351
1-Dodecanol, ACS reagent, >=98.0%
NCGC00164341-01
NCGC00164341-02
NCGC00164341-03
NCGC00253987-01
NCGC00259673-01
CS-16955
1-Dodecanol 100 microg/mL in Acetonitrile
DB-003637
1-Dodecanol, SAJ special grade, >=97.0%
1-Dodecanol, Selectophore(TM), >=98.0%
D0978
FT-0607710
FT-0693265
Oxo alcohol still bottoms (C8-18 alcohols)
ST51046177
1-Dodecanol, Vetec(TM) reagent grade, 98%
EN300-20043
C02277
Q161617
Q-200121
Dodecan-1-ol;Dodecyl alcohol;Lauryl alcohol;Dodecanol

Lauryl Myristyl Alcohol (C12-14)
Lauryl Myristyl Alcohol, also known as C12-14 Alcohol, is a fatty alcohol. It’s C1214 chain length allows it to be used in a variety of industries and applications ranging from Industrial and Personal Care to Textile and Household cleaners.

Grade

Industrial
Other Names

Dodecanol
Tetradecanol
Hexadecanol
C12-14
Form

Liquid
Abbreviations

C12-14

USAGE: Alcohols, Cleaners, Coatings, Cosmetics, Disinfectants, Fatty Alcohols, HI&I Industry, Household Care, Industrial, Inks, Lubricants, Oilfield Chemicals, Oleochemicals, Paints, Personal Care, Plastics, Polymers, TextileCategory: Alcohols, OleochemicalsType: Oleochemicals

APPLICATIONS
Consumer Products
Blends
Detergents
Ethoxylation
Household Cleaners
Sulfonation
Surfactants
Personal Care
Blends
Cosmetics
Esters
Skincare
Solvents
Surfactants


WHAT IS A FATTY ALCOHOL? 
We all know something about alcohol. 
The human race has waxed lyrical about various concoctions containing alcohol that have livened up many a party. 
Whisky (from the Gaelic Uisqe Beagh meaning water of life), contains about 40% alcohol as ethanol (ethyl alcohol). 
Alcohols occur as straight carbon chains with one or more hydroxyl (-OH) groups attached and, in exactly the same way as was outlined previously, there is a series of alcohol homologues distinguished by increasing carbon chain length. 
Some examples which might be familiar are the aforementioned Ethanol, which has a 2-carbon chain; Octanol, where the carbon chain is eight carbons in length; Lauryl alcohol (dodecanol) with 12 carbons; Cetyl alcohol (hexadecanol) with 16 carbons and Stearyl alcohol (octadecanol) with 18. 
The lower chainlengths (C2-C10) are liquid at room temperature, whereas above C10 they vary from low melting colourless crystalline materials to white waxy solids (C16-C18), melting around 55°C. 
Those of you who take the time to read product labels in supermarkets cannot have failed to have encountered these materials in detergents, shampoos or cosmetics. 
We will now focus a little more on the straight-chain alcohols generally produced from oils and fats. 
It is important to remember though that other types of alcohol exist. 
Production from petrochemicals gives rise to branched chain alcohols as well as straight chain species and it is also possible to have alcohols with more than one -OH, called polyhydric alcohols, much used in the manufacture of resins. 
A very important member of the last class is 1, 2, 3-propanetriol (or glycerine to most of us). 
This is such an important material in the oleochemicals industry that we will include a few words on its manufacture and uses later on. 
With the -OH at the end of the carbon chain, we get what is known as a primary alcohol and all of the materials we shall discuss fall into this category. 
With branched chain materials, the -OH can be surrounded by two or even three carbon chains, giving rise to secondary and tertiary alcohols respectively. 


HOW DO WE GET ALCOHOLS FROM OILS AND FATS? 
There are a number of ways that fatty alcohols can be obtained from fats and oils. 
Most involve reaction with hydrogen at high temperature and pressure and so require specialist plant to conduct the reactions safely. 
There are two main ways of working with fats and oils directly. 
Probably the oldest process is sodium reduction where metallic sodium is slurried in a solvent such as xylene and the triglyceride oil, a reducing alcohol (such as cyclohexanol) and more solvent are added to the reactor. 
The reaction occurs at about one atmosphere pressure and, in a second stage, the reaction mixture is dropped into water to hydrolyse the sodium alkoxides formed. 
The solvent and reducing alcohols are recovered by distillation for re-use and the by-product alcohol is generally fractionated to give the appropriate chainlength ranges commensurate with planned usage. 
This process has the advantage of retaining the unsaturation of the parent oil and gives very pure product. 
The disadvantages are high operating costs (due to the consumption of metallic sodium) and the elaborate equipment needed to recover both the solvent and the reducing alcohol. 

OLEOCHEMICALS - FATTY ALCOHOLS 
Oils and fats can be converted directly to alcohols by hydrogenolysis in which process the triglycerides are hydrogenated at high temperature and pressure in the presence of specific catalysts. 
A mixture of fatty alcohols and glycerine results and, again, there is a significant amount of equipment and effort needed to separate these products before the alcohol is obtained and fractionated. 
In a variation of the above process, called methanolysis, the triglycerides are reacted with methanol in the presence of a base catalyst. 
Fatty acid methyl esters and glycerine are formed and, after removing the glycerine, the esters are hydrogenated to make the alcohols which are fractionated as before. 
As methyl esters themselves have grown in importance, it is now possible to purchase these as the intended feedstock for hydrogenation and short-cut the process above with the advantage of not having to separate and deal with the glycerine. 
Similarly, triglyceride oils can be hydrolysed to fatty acids and the acids catalytically hydrogenated to alcohols and variation of catalysts and conditions can permit the retention of any unsaturation, if desired. 2

USES OF FATTY ALCOHOLS
Almost uniquely for oleochemicals, alcohols are sometimes less known by their common or chemical name, but more by their use. 
Thus, we often see the light-cut alcohols (C6-C10) called plasticizer range alcohols and C12- C18 known as detergent range alcohols. 
That gives us a clue to two of the major uses, but there are many more. Detergent uses in one form or other consume the largest proportion of alcohol produced. 
This usage depends on the ability of the alcohol to add fat-loving or lipophilic character to the detergent molecule. 
Alcohols are successful here and also provide, via the hydroxyl group, a reactive site which can add water-loving (hydrophilic) character of varying intensity depending on which chemical groupings get reacted into the molecule. 
This hydrophilic-lipophilic balance (or HLB) is key in identifying which detergents are good for removing fatty soiling and which remove non-fatty material. 
The HLB is generally modified through sulphation (reaction with sulphur trioxide in some form) to produce an alcohol sulphate, or through ethoxylation (reaction with ethylene oxide) to produce ethoxylates which can then be sulphated and used as is. 
These sulphates and ethoxylates are the active cleansing ingredients in laundry detergents, shampoos and shower gels. 
In cosmetics and pharmaceuticals, we find alcohols being used as is because of their own specific properties, usually as emollients. 
For example, Cetyl (C16) alcohol is important in cleansing, shaving and vanishing creams, hair lotions, and lipsticks. 
Cetyl and Stearyl (C18) alcohol bring similar properties to antihistamine creams, bath preparations and dermatologic bases. 
Beyond this, fatty alcohols provide the starting point for chemicals used as defoamers, emulsion stabilisers, evaporation control agents, metal working lubricants, corrosion inhibitors, fire retardants, inks and perfumes - a wide-ranging (but still not exhaustive) list indeed.

Fatty alcohols are artificially prepared with chemical compounds derived from plant and animal fats. 
Fatty alcohols are oily liquids named as oleochemicals as they produce from natural oil and fats like vegetable oils and waxes. 
Fatty alcohol is likewise derived from petrochemicals by synthetically processing ethylene. Lauryl myristyl alcohol is originated from South Africa. 
Lauryl myristyl alcohol is a type of fatty alcohol which is a form of the combination of C12 and C14 that is lauryl and myristyl. 
Lauryl myristyl alcohol is also known as DodecanolTetradecanol. The chemical formula of lauryl myristyl alcohol is C26H54O, and the molecular weight is 186.3368. 
Lauryl myristyl alcohol is colorless liquid and has a mild odor and decomposes when subjected to excessive heat. 
The life span of Lauryl myristyl alcohol is one year from its date of manufacturing. 
The Lauryl myristyl alcohol has extensive uses in several industries including food, cosmetic, automotive, textile, and chemical industries. 
Moreover, Lauryl Alcohol is used as an intermediate in the manufacture of surfactants.


Global lauryl myristyl market alcohol is driven by rising chemical and manufacturing industries. 
The wide range of application in various industries leads to increase the demand for lauryl myristyl alcohol. 
The consumers are using more of personal care products which further leads to increase in usage lauryl myristyl alcohol in cosmetics. 
Macroeconomic factors such as increasing disposable income, literacy rate, the rapid rate of urbanization, and change in lifestyle also lead to the growth of lauryl myristyl alcohol market. 
The lauryl myristyl alcohol causes corrosive of ingestion, irritation to skin and eye contact, inhalation problem

Global Lauryl alcohol Segmentation:
Based on uses, the global Lauryl myristyl alcohol market is segmented into:

Surfactants and Easters
Lubricants and Greases
Personal Care
Soaps and Detergents
Metal cleaners
Pulp and Paper Processing


Based on end-use industry, the global Lauryl myristyl alcohol market is segmented into:

Cosmetics Industry
Chemical Industry
Automotive Industry
Textile Industry
Petrochemical Industry
Ceramics industry
Pharmaceuticals Industry
Construction Industry
Based on Product type, the global Lauryl myristyl alcohol market is segmented into:

Additives
Chemicals
Metallic Stearates
Oleochemicals
Pigments
Polymers
PVC Heat Stabilizers
Titanium Dioxide


Fatty alcohols, derived from natural fats and oils, are high molecular straight chain primary alcohols. 
They include lauryl (C12), MyrIstyl (C14), Cetyl ( or palmityl: C16), stearyl (C18), Oleyl (C18, unsaturated), and Linoleyl (C18, polyunsaturated) alcohols. 
There are synthetic fatty alcohols equivalent physically and chemically to natural alcohols obtained from oleochemical sources such as coconut and palm kernel oil. 
Fatty alcohols are emulsifiers and emollients to make skin smoother and prevent moisture loss. 
Identical fatty esters are used to improve rub-out of formulas and to control viscosity and dispersion characteristics in cosmetics, personal care products and pharmaceutical ingredients. 
As chemical intermediates, the primary use of fatty alcohols are as raw material for the production of fatty sulfate salts and alcohol ethoxylates for foaming and cleaning purposes in the field of detergent industry. 
Chemical reactions of primary alcohols include esterifications, ethoxylation, sulfation, oxidation and many other reactions. 

Their derivatives and end use applications include;
•    Nonionic surfactants (Ethoxylates and propoxylates)
•    Anionic surfactants (Alkyl sulfates and alkyl ethoxy sulfates)
•    Chemical intermediates and  polymerization modifiers (Alkyl halides, Alkyl mercaptans)
•    Quaternary ammonium compounds for detergent sanitisers, softner for textiles, phase transfer catalyst and biocides
•    Antioxidants for plastics (Alkyl thiopropionates and alkyl phosphites)
•    Lubricant additives (Metallic and thio alkylphosphates)
•    Flavor and Fragrance (Aldehydes and ketones)
•    PVC plasticizers (Dialkyl Phthalates, adipates and trimellitates)
•    Coatings and inks (acrylate and methacrylate esters)
•    Water treatment (acrylate and methacrylate esters)

Large amount of fatty alcohols are used as special solvents, fillers in plasticizer and insulating materials for the building industry. 
Fatty alcohols are used as ingredients in the industries of agricultural, foodstuff, metal processing, cosmetics, lube additive, pharmaceutical, rubber, textile, perfume and flavouring as well as synthetic detergent.


1-Dodecanol
Dodecan-1-ol
Dodecan-1-ol
dodecan-1-ol


CAS names
1-Dodecanol
IUPAC names
1-Dodecanol
1-dodecanol
1-Dodecanol
Alcohol C12
Alcohol, C12
Dodecan-1-ol
dodecan-1-ol
Dodecan-1-ol
dodecan-1-ol
Dodecyl alcohol
Fatty alcohols comprising of: Dodecan-1-ol
Lauryl alcohol
Palmerol 1214 NF
Palmerol 1216

Trade names
CO-1214
CO-1270
ECOROL 02
ECOROL 12/98
ECOROL 12/99
ECOROL 24
ECOROL 24/55
ECOROL 26
ECOROL 28
Fatty alcohol 12 
Fatty alcohol 1214 
Fatty alcohol 1216 
Kalcol
Lauryl Alcohol
Leunapol-FA 12
Nacol 12 
Nafol 1214 

MYRISTYL ALCOHOL (C14)
Myristyl alcohol is a  long-chain fatty alcohol that is tetradecane in which one of the terminal methyl hydrogens is replaced by a hydroxy group


1-Tetradecanol, or commonly myristyl alcohol (from Myristica fragrans – the nutmeg plant), is a straight-chain saturated fatty alcohol, with the molecular formula C14H30O. 
It is a white crystalline solid that is practically insoluble in water, soluble in diethyl ether, and slightly soluble in ethanol.

1-Tetradecanol may be prepared by the hydrogenation of myristic acid (or its esters); myristic acid itself can be found in nutmeg (from where it gains its name) but is also present in palm kernel oil and coconut oil and it is from these that the majority of 1-tetradecanol is produced.
It may also be produced from petrochemical feedstocks via either the Ziegler process or hydroformylation.

As with other fatty alcohols, 1-tetradecanol is used as an ingredient in cosmetics such as cold creams for its emollient properties. 
It is also used as an intermediate in the chemical synthesis of other products such as surfactants.

Myristyl Alcohol helps to stabilize the product formulation while softening the upper layer of the skin. 

1-Hydroxytetradecane    
1-Tetradecanol    
1-Tetradecyl alcohol    
Myristic alcohol    
Myristyl alcohol    
n-Tetradecanol    
n-Tetradecanol-1    
n-Tetradecyl alcohol    
tetradecan-1-ol    
tetradecanol    
Tetradecyl alcohol


MYRISTYL ALCOHOL is classified as :
Emollient
Emulsion stabilising
Foam boosting
Skin conditioning
Viscosity controlling
CAS Number: 112-72-1
EINECS/ELINCS No: 204-000-3
Chem/IUPAC Name: Tetradecanol

Name: 1-Tetradecanol
Synonyms    
Alcohol C-14
n-Tetradecyl alcohol
Tetradecan-1-ol
Myristyl alcohol
Myristic alcohol
Tetradecanol
CAS: 112-72-1
EINECS: 204-000-3

- Vegetable origin
- Colourless liquid product with typical fatty alcohol odour.
- Used directly as foam stabilizer, detergency boosting & lubricant additives.
- Major Application in manufacture of Chemical Intermediates, Surfactants and Textile chemicals.


Cosmetic Uses:    
emulsion stabilisers
skin conditioning
skin conditioning - emollient
surfactant - foam boosting
viscosity controlling agents

Myristyl alcohol has emollient and emulsion stabilising properties, and it is used in some skincare formulations to help moisturise the skin as well as prevent the soluble ingredients from separating.


Other names: 1-Tetradecanol, 1-Hydroxytetradecane

INCI Name:
Myristyl Alcohol
Ingredient origins:
Oil Palm Fruit, Hydrocarbons
Role:
Emollient, Surfactant
Common name:
Myristyl Alcohol

C14H29OH Liquid boiling at 264°C; soluble in ether and alcohol, insoluble in water; used as a chemical intermediate, plasticizer, and perfume fixative.


Use: Pharmaceuticals and Cosmetics use : 

MYRISTYL ALCOHOL is Emulsion stabilizer for creams and lotions. 
MYRISTYL ALCOHOL is Quality modifier of lipsticks. 
MYRISTYL ALCOHOL is an additive for ointment base and cream conditioners. 
MYRISTYL ALCOHOL is the smooth touch ingredient to skin for cosmetic uses. It is Auxiliary for emulsifiers.MYRISTYL ALCOHOL has thickening properties in cosmetics products.

Use: Cosmetics and Personal Care, Cleaning and Detergents

Synonyms:
     dytol R-52
1-    hydroxytetradecane
     kalcohl 40
     kalcohl 4098
     lanette wax KS
     loxanol V
     myristic alcohol
     nacol 14-95
     tetradecan-1-ol
N-    tetradecan-1-ol
     tetradecanol
1-    tetradecanol
N-    tetradecanol
N-    tetradecanol-1
     tetradecyl alcohol
N-    tetradecyl alcohol

Fatty alcohols like MYRISTYL ALCOHOL have many uses in today’s manufacturing facilities. Myristyl Alcohol is often employed as a chemical intermediate when producing surfactants, detergents and esters used in cleaning products. 
As well, Myristyl Alcohol possesses natural foaming stabilizing and amphipathic properties, adding to their usefulness as a detergent or soap. 
Other uses of myristyl Alcohol include as an emollient, emulsifier or viscosity modifier in cosmetics and personal care products, as well as in lubricants and greases. 
Myristyl Alcohol can also be used to process textiles.

Applications
1-Tetradecanol is used as an ingredient in cosmetics such as cold creams. 1-Tetradecanol is an active intermediate in the chemical synthesis of sulfated alcohol. 
1-Tetradecanol is also employed in the fabrication of temperature-regulated drug release system based on phase-change materials. 
1-Tetradecanol plays a vital role in filling the hollow interiors of gold nanocages in the fabrication of new theranostic system, which has unique feature of photoacoustic imaging.

Notes
Incompatible with strong oxidizing agents, acid chlorides and acid anhydrides. Store in a cool place

Usage/Application: Surfactant, Thickener and emulsion stabilizer, Emollient in cosmetics


Myristyl alcohol has emollient, viscosity controlling, emulsion stabilising properties in cosmetics products.

Myristic alcohol or Tetradecanol is a fatty alcohol used in cosmetics as an emollient (helps water and oil to mix). 
Myristyl alcohol is produced from coconut, palm kernel and nutmeg oil. Myristyl alcohol is authorized organically.

Functions of MYRISTYL ALCOHOL (INCI)
Emollient: Softens and softens the skin
Emulsion stabilizer: Promotes the emulsification process and improves the stability and shelf life of the emulsion
Foam Sinergiste: Improves the quality of the foam produced by increasing one or more of the following properties: volume, texture and / or stability
Skin care agent: Keeps the skin in good condition
Viscosity control agent: Increase or decrease the viscosity of cosmetics


Preferred IUPAC name: Tetradecan-1-ol

Other names: Myristyl alcohol, Tetradecyl alcohol

Identifiers
CAS Number: 112-72-1 


Properties
Chemical formula: C14H30O
Molar mass: 214.393 g·mol−1
Density: 0.824 g/cm³
Melting point: 38 °C (100 °F; 311 K)
Boiling point: >260 °C


Tetradecanol is a colorless thick liquid (heated) with a faint alcohol odor. Solidifies and floats on water. (USCG, 1999)


Tetradecan-1-ol is a long-chain fatty alcohol that is tetradecane in which one of the terminal methyl hydrogens is replaced by a hydroxy group 
It is a long-chain primary fatty alcohol, a fatty alcohol 14:0 and a primary alcohol.

Myristyl alcohol (C14)
CAS Nr.
112-72-1


Myristyl alcohol may be prepared by the hydrogenation of Myristic acid (or its esters); Myristic acid itself can be found in nutmeg (from where it gains its name) but is also present in palm kernel oil and coconut oil and it is from these that the majority of Myristyl alcohol is produced

Industries / Applications
Chemical Derivatives of Myristyl alcohol: 
• APGs
• Sulfates
• Esters
• Alkoxylates
• Ether sulfates
Household Care:
• Esters
• Alkoxylates
• Ether sulfates
• APGs
• Sulfates
Industrial & Institutional Cleaners:
• Alkoxylates
• Ether sulfates
• APGs
• Sulfates
• Esters
Lubricants and Greases:
• Phosphate esters for extreme pressure additives
Oilfield Chemicals:
• Esters
• Ethoxylates
Paints, Coatings & Inks:
• Glycidyl ether reactive diluents for epoxy resins
Polymers & Plastics:
• Glycidyl ether reactive diluents for epoxy resins
Textile Chemicals:
• Ethoxylates
• Esters


Myristyl alcohol is a lighter-weight fatty alcohol that functions as a thickener, emulsion stabilizer, and emollient. 
Myristyl alcohol is also sometimes used as a surfactant, often with other surfactants. Myristyl alcohol is considered safe as used in cosmetics.

Myristyl Alcohol is a fatty-alcohol used as an emollient in cosmetics and skin care products. 
Myristyl Alcohol is primarily used to inhibit a formula from separating into its oil and liquid components

Myristyl Alcohol is also used as an intermediate in the manufacture of surfactants.


Myristyl Alcohol is used in some Shampoos due to its foam boosting and viscosity stabilizing properties. 
Commonly Myristyl Alcohol is used in cosmetics (Hair care, skincare, body care) as an emollient and a stabilizer, preventing separation. 
Myristyl Alcohol smooths the skin and prevents moisture loss. Myristyl Alcohol may also be used as a fragrance ingredient.


1-Tetradecanol Chemical Properties, Uses, Production

Description
1-Tetradecanol is a kind of straight-chain saturated fatty alcohol. It is often used as an ingredient in cosmetics such as cold creams because of its emollient properties. 
Myristyl alcohol can also be used as the intermediate during the manufacturing of some organic compounds like surfactants. 
Some studies have shown that it can inhibit the endothelial activation and reduce tissue responsiveness to cytokines, having the potential to treat the periodontitis based on studies on rabbits. It is also employed for the fabrication of temperature-regulated drug release system based on phase-change materials.

Chemical Properties
Myristyl alcohol occurs as a white crystalline solid with a waxy odor. Also reported as opaque leaflets or crystals from ethanol.

Chemical Properties
white low melting solid or flakes

Uses
As emollient for cold creams, etc., also for making the sulfated alcohol whose sodium salt is applicable as a "wetter" in textiles.

Uses
myristyl alcohol is an emollient often used in hand creams, cold creams, and lotions to give them a smooth, velvety feel. Sources indicate it as being mildly comedogenic and potentially irritating.

Production Methods
Myristyl alcohol is found in spermaceti wax and sperm oil, and may be synthesized by sodium reduction of fatty acid esters or the reduction of fatty acids by lithium aluminum hydride. It can also be formed from acetaldehyde and dimethylamine.

Definition
ChEBI: A long-chain fatty alcohol that is tetradecane in which one of the terminal methyl hydrogens is replaced by a hydroxy group

Synthesis Reference(s)
The Journal of Organic Chemistry, 35, p. 1210, 1970 DOI: 10.1021/jo00829a089

General Description
Colorless thick liquid (heated) with a faint alcohol odor. Solidifies and floats on water.

Air & Water Reactions
Insoluble in water.

Reactivity Profile
1-Tetradecanol is an alcohol. Flammable and/or toxic gases are generated by the combination of alcohols with alkali metals, nitrides, and strong reducing agents. They react with oxoacids and carboxylic acids to form esters plus water. Oxidizing agents convert them to aldehydes or ketones. Alcohols exhibit both weak acid and weak base behavior. They may initiate the polymerization of isocyanates and epoxides.

Health Hazard
Low toxicity. Overexposure causes some central nervous system depression. Prolonged skin contact causes skin irritation.

Pharmaceutical Applications
Myristyl alcohol is used in oral, parenteral, and topical pharmaceutical formulations. It has been evaluated as a penetration enhancer in melatonin transdermal patches in rats.
Myristyl alcohol has also been tested as a bilayer stabilizer in niosome formulations containing ketorolac tromethamine,and zidovudine.Niosomes containing myristyl alcohol showed a considerably slower release rate of ketorolac tromethamine than those containing cholesterol.This was also observed with the zidovudine formulation.

Safety
Myristyl alcohol is used in oral parenteral, and topical pharmaceutical formulations. The pure form of myristyl alcohol is mildly toxic by ingestion and may be carcinogenic; experimental tumorigenic data are available.It is also a human skin irritant. In animal studies of the skin permeation enhancement effect of saturated fatty alcohols, myristyl alcohol exhibited a lower effect when compared with decanol, undecanol, or lauryl alcohol but caused greater skin irritation.A study investigating contact sensitization to myristyl alcohol revealed that patch testing of myristyl alcohol 10% petrolatum should not be carried out owing to observed irritant effects; thus the use of a lower concentration of myristyl alcohol for such tests (5% petrolatum) was recommended.Myristyl alcohol has been associated with some reports of contact allergy.(8,9)A moderate-to-severe erythema and moderate edema are seen when 75 mg is applied to human skin intermittently in three doses over 72 hours.
LD50(rabbit, skin): 7.1 g/kg
LD50(rat, oral): 33.0 g/kg

storage
The bulk material should be stored in a well-closed container in a cool, dry place.

Purification Methods
Crystallise the alcohol from aqueous EtOH. It has also been purified by zone melting. [Beilstein 1 IV 1864.]

Incompatibilities
Myristyl alcohol is combustible when exposed to heat or flame. It can react with oxidizing materials. When heated to decomposition, it emits acrid smoke and irritating fumes.

Regulatory Status
Included in the FDA Inactive Ingredients Database (oral tablet: sustained-release; and topical formulations: cream, lotion, suspension). Included in nonparenteral (topical cream) formulations licensed in the UK.
1-Tetradecanol Preparation Products And Raw materials

Raw materials
Myristic acid MYRISTYL MYRISTATE
Preparation Products
1-Bromotetradecane FEMA 2763


MYRISTYL ALCOHOL (C14)

APPLICATIONS
Consumer Products
Blends
Detergents
Ethoxylation
Household Cleaners
Sulfonation
Surfactants
Flavors & Fragrances
Fragrance Additives
Personal Care
Blends
Cosmetics
Esters
Skincare
Surfactants


 fatty-alcohol emollient

* Also known as 1-Tetradecanol

Functions:

Myristyl Alcohol is a fatty-alcohol used as an emollient in cosmetics and skin care products. 
According to research, it is primarily used to inhibit a formula from separating into its oil and liquid components. 

Myristyl Alcohol is also used for other properties, including as an: Emulsion Stabilizer; Skin-Conditioning Agent; Surfactant; Viscosity Increasing Agent; Foaming Agent; and Fragrance Ingredient. 
Myristyl Alcohol provides a fruity, coconut scent.

    
tetradecan-1-ol is a fatty alcohol 14:0 
tetradecan-1-ol is a long-chain primary fatty alcohol 
tetradecan-1-ol is a primary alcohol 
    
myristyl palmitate has functional parent tetradecan-1-ol 
tetradecyl tetradecanoate has functional parent tetradecan-1-ol 

What Is It?
Cetearyl Alcohol, Cetyl Alcohol, Myristyl Alcohol and Behenyl Alcohol are white, waxy solids. Isostearyl Alcohol is a clear liquid. Cetyl Alcohol and Stearyl Alcohol are the two major components of Cetearyl Alcohol. These ingredients are all fatty alcohols and that are widely used in cosmetics and personal care products, especially in skin lotions and creams.

Why is it used in cosmetics and personal care products?
Cetearyl Alcohol and the other fatty alcohols keep an emulsion from separating into its oil and liquid components. These ingredients are also used to alter the thickness of liquid products and to increase foaming capacity or to stabilize foams.

Scientific Facts: 
Cetearyl, Cetyl, Myristyl and Behenyl Alcohols are straight-chain alcohols. Isostearyl Alcohol is a branched chain alcohol. Cetearyl Alcohol is a mixture of mostly of Cetyl and Stearyl Alcohols, which are fatty alcohols that occur naturally in small quantities in plants and animals.

Myristyl Alcohol is a 14 carbon chain. Cetyl Alcohol has 16 carbons, while Stearyl and Isostearyl Alcohols have 18 carbons. Behenyl Alcohol is the largest fatty alcohol in this group with 22 carbons.


Myristyl Alcohol
What: Myristyl Alcohol is a saturated fatty alcohol found in natural oils often used in cosmetics as an emollient and a stabilizer, preventing separation. Myristyl Alcohol smooths the skin and prevents moisture loss (Wiki).

Myristyl Alcohol may also be used as a foaming agent and fragrance ingredient.

Origin: Myristyl Alcohol is derived from natural fats and oils found in palm kernel oil, coconut oil, and nutmeg.

Products Found In: Hair care, skincare, body care, sunless tanners, perfumes.

Alternate Names: 1-Hydroxytetradecane; Tetradecanol; 1-Tetradecanol; Tetradecyl Alcohol; Dytol R-52; Lanette Wax Ks; Loxanol V; Myristic Alcohol; Myristyl Alcohol (Mixed Isomers) ; N-Tetradecanol-1; N-Tetradecyl Alcohol.

Toxicity: Myristyl Alcohol is generally classified as having low toxicity.(EWG).

Cetearyl, Cetyl, Myristyl, and Behenyl alcohols are straight-chain aliphatic alcohols. Isostearyl Alcohol is a branched-chain aliphatic alcohol.


Cetearyl Alcohol
Cetearyl Alcohol (CAS No. 8005-44-s) is a white, waxy solid, usually in flake form. It is a mixture of mostly cetyl (hexadecanol) and stearyl (octodecanol) alcohols. 
Cetearyl Alcohol is also known as cetostearyl alcohol and cetyl/ stearyl alcohol. It is insoluble in water and soluble in alcohol and oils.

Cetyl Alcohol
Cetyl Alcohol (CAS No, 36653-82-4) is a white, waxy solid in flake or powder form.
It is a 16-carbon alcohol, known also as 1 -hexadecanol and n-hexadecyl alcohol. Cetyl Alcohol is the oldest known of the long-chain alcohols, having been discovered by Chevrenl in 1913.  
It is insoluble in water and soluble in alcohol and oils.

lsostearyl Alcohol
lsostearyl Alcohol (CAS No. 27458-93-l and 41744-75-6) is a clear waterwhite liquid, consisting essentially of a mixture of branched-chain, aliphatic 18- carbon alcohols.
It is a primary alcohol having monomethyl branching randomly distributed along its C,, straight chain. 
lsostearyl Alcohol is insoluble in water and miscible in most oils and waxes.

Myristyl Alcohol
Myristyl Alcohol (CAS No. 112-72-I) or 1-tetradecanol is a white unctuous mixture of solid alcohols consisting chiefly of 14carbon alcohols (n-tetradecanol); it is soluble in ether, slightly soluble in ethanol, and insoluble in water

Behenyl Alcohol
Behenyl Alcohol or n-docosanol (CAS No. 661-l 9-8) is a 22-carbon aliphatic alcohol. It is a colorless, waxy solid that is soluble in ethanol and chloroform and insoluble in water.


Impurities
Cetearyl Alcohol
Technical grade Cetearyl Alcohol contains approximately 65% to 80% stearyl and 20% to 35% cetyl alcohols. 
Though Cetearyl Alcohol consists mostly of cetyl and stearyl alcohols, small quantities of alcohols with longer and shorter chain lengths are usually present in this mixture.
Additionally, the following impurities have been reported for Cetearyl Alcohol mixtures.
Hydrocarbons (consisting principally of n-hexadecane and n-octadecane) 0.1-l .4%
Odd-numbered straight-chain alcohols l-3.5%
Branched-chain primary alcohols 0.2-2%
Even-numbered straight-chain alcohols (C,-C,,) comprise 90% to 95% of this mixture.

Cetyl Alcohol
Cetyl Alcohol (National Formulary) contains a minimum of 90% Cetyl Alcohol ) Cetyl Alcohol is generally believed to be l-hexadecanol, but commercial grades often contain measurable amounts of stearyl alcohol and other longchain aliphatic alcohols. The Cosmetic, Toiletry and Fragrance Association (CTFA) Specification for Cetyl Alcohol includes the following impurities:
Hydrocarbons 1.5% maximum
Ash 0.05% maximum
Lead (as elemental lead) 20 ppm maximum
Arsenic (as elemental arsenic) 3 ppm maximum

lsostearyl Alcohol
Published data concerning impurities within lsostearyl Alcohol mixtures have not been identified.

Myristyl Alcohol
The CTFA Specification for Myristyl Alcohol includes the following impurities :
Hydrocarbons
Ash
Lead (as elemental lead)
Arsenic (as elemental arsenic)
1.5% maximum
0.05% maximum
20 ppm maximum
3 ppm maximum

Behenyl Alcohol
Technical grade Behenyl Alcohol contains 99% Behenyl Alcohol. 

1-TETRADECANOL
Tetradecan-1-ol
Myristyl alcohol
112-72-1
Tetradecanol
Tetradecyl alcohol
n-Tetradecanol
Myristic alcohol
n-Tetradecyl alcohol
Lanette K
Loxanol V
Lanette Wax KS
n-Tetradecanol-1
1-Hydroxytetradecane
Alfol 14
n-Tetradecan-1-ol
Dytol R-52
Alcohols, C10-16
Alcohols, C12-16
Alcohols, C14-15
Lanette 14
1-Tetradecyl alcohol
tetradecan1-ol
NSC 8549
MFCD00004757
UNII-V42034O9PU
Myristyl alcohol [NF]
67762-41-8
68855-56-1
CHEBI:77417
V42034O9PU
kalcohl 40
75782-87-5
Myristyl alcohol (NF)
1-Tetradecanol, 99%
DSSTox_CID_6926
DSSTox_RID_78257
DSSTox_GSID_26926
C14 alcohol
Alcohol(C14)
Alcohols, C>14
Fatty alcohol(C14)
Alcohols, C12-15
CAS-112-72-1
Tetradecanol (7CI)
C12-16 Alcohols
Kalcohl 4098
C14-15 alcohol
HSDB 5168
Lorol C 14
Adol 18
Kalcol 4098
Conol 1495
EINECS 204-000-3
Nacol 14-95
BRN 1742652
(C10-C16) Alkyl alcohol
(C12-C16) Alkyl alcohol
tetradecylalcohol
AI3-00943
Alcohols, C14-22 and C16-22-unsatd.
Tetradecanol-1
n-tetradecylalcohol
Dehydag wax 14
EINECS 267-019-6
EINECS 268-107-7
EINECS 272-490-6
EINECS 275-983-4
1-tetradecanol group
Philcohol 1400
Lorol C14
63393-82-8
Myristyl cetyl alcohol
Epal 14
Fatty alcohol (C14)
1-Tetradecanol, 97%
CCCCCCCCCCCCCC[O]
SDA 15-060-00
ACMC-1BY8P
EC 204-000-3
EC 616-261-4
(C14-C18)Alkyl alcohol
SCHEMBL20286
4-01-00-01864 (Beilstein Handbook Reference)
68002-95-9
71750-71-5
(C14-C18) Alkyl alcohol
(C14-C18)-Alkyl alcohol
CHEMBL24022
(C14-C22) and (C16-C22)Unsaturated alkylalcohol
WLN: Q14
DTXSID9026926
NSC8549
Mixed fatty alcohols (C10-C16)
NSC-8549
ZINC1644076
EINECS 267-009-1
EINECS 269-790-4
Tox21_201842
Tox21_300538
ANW-16516
LMFA05000041
SBB060166
STL453593
AKOS009031495
CS-W004294
MCULE-8719320111
NCGC00164345-01
NCGC00164345-02
NCGC00164345-03
NCGC00254322-01
NCGC00259391-01
BP-30124
1-Tetradecanol, purum, >=95.0% (GC)
FT-0608311
ST51046400
1-Tetradecanol, Selectophore(TM), >=99.0%
D05097
1-Tetradecanol, Vetec(TM) reagent grade, 97%
Q161683
F7FCB87C-0FA4-412A-BC8C-BE5C952BC1E0
J-002824
Myristyl alcohol, United States Pharmacopeia (USP) Reference Standard
Myristyl Alcohol, Pharmaceutical Secondary Standard; Certified Reference Material


Fatty alcohols are artificially prepared with chemical compounds derived from plant and animal fats. 
Fatty alcohols are oily liquids named as oleochemicals as they produce from natural oil and fats like vegetable oils and waxes. 
Fatty alcohol is likewise derived from petrochemicals by synthetically processing ethylene. 
Lauryl myristyl alcohol is originated from South Africa. 
Lauryl myristyl alcohol is a type of fatty alcohol which is a form of the combination of C12 and C14 that is lauryl and myristyl. 
Lauryl myristyl alcohol is also known as DodecanolTetradecanol. 
The chemical formula of lauryl myristyl alcohol is C26H54O, and the molecular weight is 186.3368. 
Lauryl myristyl alcohol is colorless liquid and has a mild odor and decomposes when subjected to excessive heat. 
The life span of Laurel myristyl alcohol is one year from its date of manufacturing. 
The Lauryl myristyl alcohol has extensive uses in several industries including food, cosmetic, automotive, textile, and chemical industries. 
Moreover, Lauryl Alcohol is used as an intermediate in the manufacture of surfactants.


Global lauryl myristyl market alcohol is driven by rising chemical and manufacturing industries. 
The wide range of application in various industries leads to increase the demand for lauryl myristyl alcohol. 
The consumers are using more of personal care products which further leads to increase in usage lauryl myristyl alcohol in cosmetics. 
Macroeconomic factors such as increasing disposable income, literacy rate, the rapid rate of urbanization, and change in lifestyle also lead to the growth of lauryl myristyl alcohol market.
The lauryl myristyl alcohol causes corrosive of ingestion, irritation to skin and eye contact, inhalation problem. 
Severe overexposure can cause death leads to restraining the growth of the market.


Global Lauryl myristyl alcohol: Regional Outlook:

The global Lauryl myristyl alcohol is segmented into seven regions includes North America, Latin America, Asia-Pacific excluding Japan, Eastern Europe, Western Europe, Japan and The Middle East and Africa. 
Asia Pacific is expected to be the fastest growing Lauryl myristyl alcohol regional market. 
Moreover, the Asia Pacific and Japan has shown the growth in Lauryl myristyl alcohol market owing to rise in demand for the food and cosmetic industry in the region. 
European Lauryl myristyl alcohols market is expected to decline share to high growth in areas such as Asia Pacific and Latin America. 
The uncertain economic circumstance in the region combined with declining growth in the main downstream industries is relied upon to have an adversely affect the Lauryl myristyl alcohols market. 
North America Lauryl myristyl alcohols market is foreseen to witness average growth over the anticipated period due to expanding the bio-based product.

Based on uses, the global Myristyl alcohol market is segmented into:

Surfactants and Easters
Lubricants and Greases
Personal Care
Soaps and Detergents
Metal cleaners
Pulp and Paper Processing

Based on end-use industry, the global Myristyl alcohol market is segmented into:

Cosmetics Industry
Chemical Industry
Automotive Industry
Textile Industry
Petrochemical Industry
Ceramics industry
Pharmaceuticals Industry
Construction Industry

Based on Product type, the global Myristyl alcohol market is segmented into:

Additives
Chemicals
Metallic Stearates
Oleochemicals
Pigments
Polymers
PVC Heat Stabilizers
Titanium Dioxide

Based on Agent, the global Myristyl alcohol is segmented into

Emulsion
Stabilizer
Thickener


Lauryl Myristyl Alcohol

CAS No.: 80206-82-2

Synonyms: Dodecanol Tetradecanol

Lauryl Myristyl Alcohol is used as an intermediate in the manufacture of surfactants.


Lauryl/myristyl alcohol is a mix of C12 (laurel alcohol) and C14 (myristyl alcohol) fatty alcohols. 
Used in many industrial and manufacturing processes, C12-16 alcohols can be derived from both organic and synthetic sources, though all Acme-Hardesty products are 100-percent vegetable-based and GMO-free.

Global Myristyl Alcohol Market size is likely to witness significant growth, expanding at a moderate CAGR over the forecast period. 
Myristyl alcohol, chemical name 1- Tetradecanol, is a straight chain saturated fatty alcohol. 
It is a transparent white solid which is completely soluble in diethyl ether, marginally soluble in ethanol and insoluble in water.
 

Rising disposable income, growing consumerism and increased health awareness among consumers, have been the prime drivers for cosmetics industry. 
Any trend in this industry will have a direct impact on the myristyl alcohol market size over the forecast timespan. 
Moreover, developing countries are heavily investing in pharmaceutical sector to battle out rising number of ailments and health related issues. 
This inclination towards pharmaceutical industry will further push the product demand in the coming years.
 

Detergent industry is also witnessing prominent gains due to increasing demand in emerging economies, which can be attributed to improved standard of living coupled with growing concerns for health and hygiene. 
This is expected to boost the overall myristyl alcohol market size in the years to come. 
However, growing prevalence of substitutes in industry along with oscillating raw material prices is likely to be the major challenge for myristyl alcohol market share over the forecast timespan.
 

Based on the process of manufacturing, the global myristyl alcohol market share is classified into ziegler process derived and hydrogenation process derived products. 
In case of the latter process, the product is synthesized by hydrogenation of myristic acid (its esters), which is primarily present in palm kernel and coconut oil. 
Majority of the product is produced through this process, whereas, ziegler process of manufacturing involves extracting the product from petrochemical feedstock.
 

Cosmetics was the major applications of myristyl alcohol market share in 2016. 
Other uses are in detergent and pharmaceutical industry. 
The product is extensively used as a chief ingredient in production of cold creams. 
It is used in cosmetics products in general as a fragrance ingredient. 
It is employed as an active intermediate in synthesis of sulfated alcohols. 
The product is also used in synthesis of temperature-controlled drug release systems which are based on phase alteration materials and as excipients in tropical, oral and parenteral pharmaceutical applications.
 

Other uses of the product include synthesis of theranostic systems which have exclusive characteristics of photoacoustic imaging. 
The product has a key role in filling of hollow cores of gold nanocages. 
It is also widely used in foaming agents which are used in surfactants (fatty alcohol sulfates & ethoxy sulfates and ethoxylates) in detergent manufacturing. 
Moreover, huge quantities of the product are used as special solvents and fillers in insulating materials & plasticizers for the construction industry.
 

Asia Pacific is expected to be the fastest growing region for the myristyl alcohol market over the forecast period, followed by North America and Europe. 
India and China were the prominent users of the product in Asia Pacific owing to the growing presence of end-user industries in these countries. 
Moreover, increase in consumption of edible oils across the globe is expected to drive the myristyl alcohol market in next few years. 
Japan, Vietnam, Cambodia, Republic of Korea, Malaysia, Indonesia and Australia are Asia Pacific countries offering ample of future opportunities for the industry growth over the forecast period. 
Due to saturation of myristyl alcohol market size in North American and European countries, these regions are likely to exhibit slow-paced growth by 2024.

 
1-Tetradecanol
Tetradecan-1-ol
Tetradecanol
tetradecanol
CAS names
1-Tetradecanol


IUPAC names
1-Tetradecanol
1-tetradecanol
1-Tetradecanol
1-tetradecanol
Alcohol C14
Alcohol, C14
Fatty alcohol C14
MYRISTYL ALCOHOL
Palmerol 1214 NF
Palmerol 1216

Tetradecan-1-ol
tetradecan-1-ol
Tetradecan-1-ol
tetradecan-1-ol
Tetradecanol
tetradecanol
Tetradecanol
tetradecanol

Trade names
Alcohol C14
Alfol 1214
CO-1214
CO-1270
ECOROL 14/98
ECOROL 14/99
ECOROL 24
ECOROL 24/55
ECOROL 26
ECOROL 28
Kalcol
Leunapol-FA 14
Nacol 14
Nafol 1214

Also known as:

tetradecan-1-ol
tetradecyl alcohol
1-hydroxytetradecan
n-Tetradecanol
n-Tetradecyl alcohol
n-Tetradecanol-1
Myristic alcohol
1-Tetradecyl alcohol
1-Tetradecanol
1-Hydroxytetradecane
tetradecanol
Kalcohl 4098
Lanette K
Lanette Wax KS
Lanette 14
Kalcol 4098
Nacol 14-95
Kalcohl 40
Lorol C 14
Tetradecanol (7CI)
Alfol 14
N-Tetradecan-1-ol
Conol 1495
Adol 18
Loxanol V


•    1-Tetradecanol, synthesis grade DISCONTINUED
•    Myristyl Alcohol (1 g)
•    1-Tetradecanol, 97+%
•    MYRISTYL ALCOHOL pure
•    1-TETRADECANOL FOR SYNTHESIS 1 KG
•    1-TETRADECANOL FOR SYNTHESIS 50 KG
•    1-TETRADECANOL FOR SYNTHESIS 100 G
•    1-Tetradecanol 97%
•    1-Tetradecanol Vetec(TM) reagent grade, 97%
•    1-Tetradecandol
•    Myristyl alcohol Tetradecyl alcohol
•    MYRISTYL ALCOHOL
•    MYRISTIC ALCOHOL
•    N-TETRADECYL ALCOHOL
•    TETRADECYL ALCOHOL
•    Alfol 14
•    alfol14
•    Cachalot M-43 NF
•    Dehydag wax 14
•    Dytol R-52
•    n-Tetradecanol-1
•    Philcohol 1400
•    Tetradecan-1-ol
•    Tetradecanol-1
•    dytolr-52
•    Emery 3334
•    Epal 14
•    Lanette 14
•    Lanette K
•    Lanette Wax KS
•    Lanette Waxd sub 1
•    lanettek
•    lanettewaxks
•    Lorol C14
•    Loxanol V
•    loxanolv
•    myristic
•    Myristryl alcohol
•    myristyl
•    n-Tetradecan-1-ol
•    n-Tetradecanol
•    1-TETRADECANOL
•    1-HYDROXYTETRADECANE
•    ALCOHOL C14
•    MyristylAlcohol>95%
•    1-Tetradecanol, 99+%
•    MYRISTYLALCOHOL,REAGENT
•    ALKOHOL C 14 REIN
•    1-TETRADECANOL 99+% ARGRADE, BOTTLE OF (5)-GM
•    1-TETRADECANOL, SYNTHESIS GRADE
•    1-TETRADECANOL (MYRISTYL ALCOHOL)
•    1-Tetradecanol (Myristyl Alcohol), 99+%
•    C14 Alcohol
•    1-Tetradecanol (Standard for GC,>99%)
•    6-(trideuteriomethyl)pyridine-2-carbaldehyde
•    1-Tetradecanol >
•    Tetradecanol Tetradecanol
•    1-Tetradecanol,>98%


All Fatty Alcohols Products of ATAMAN CHEMICALS:
HEXANOL (C6 ALCOHOL)
C610 ALCOHOL
OCTANOL (C8 ALCOHOL)
C810 ALCOHOL
DECANOL (C10 ALCOHOL)
LAURYL ALCOHOL (C1299)
MIDCUT ALCOHOL (C1214)
MIDCUT ALCOHOL (C1216)
MYRISTYL ALCOHOL (C14)
C1416 ALCOHOL
CETYL ALCOHOL (C16)
CETEARYL ALCOHOL (C16 CETYL/STEARYL ALCOHOL)
STEARYL ALCOHOL (C18)
ARACHIDYL (C20 ALCOHOL)
BEHENYL ALCOHOL 45 (C1822)
BEHENYL ALCOHOL 70 (C2270)


Name    Carbon atoms    Branches/saturation    Formula
tert-Butyl alcohol    4 carbon atoms    branched    C4H10O
tert-Amyl alcohol    5 carbon atoms    branched    C5H12O
3-Methyl-3-pentanol    6 carbon atoms    branched    C6H14O
1-Heptanol (enanthic alcohol)    7 carbon atoms        C7H16O
1-Octanol (capryl alcohol)    8 carbon atoms        C8H18O
Pelargonic alcohol (1-nonanol)    9 carbon atoms        C9H20O
1-Decanol (decyl alcohol, capric alcohol)    10 carbon atoms        C10H22O
Undecyl alcohol (1-undecanol, undecanol, Hendecanol)    11 carbon atoms        C11H24O
Lauryl alcohol (dodecanol, 1-dodecanol)    12 carbon atoms        C12H26O
Tridecyl alcohol (1-tridecanol, tridecanol, isotridecanol)    13 carbon atoms        C13H28O
Myristyl alcohol (1-tetradecanol)    14 carbon atoms        C14H30O
Pentadecyl alcohol (1-pentadecanol, pentadecanol)    15 carbon atoms        C15H32O
Cetyl alcohol (1-hexadecanol)    16 carbon atoms        C16H34O
Palmitoleyl alcohol (cis-9-hexadecen-1-ol)    16 carbon atoms    unsaturated    C16H32O
Heptadecyl alcohol (1-n-heptadecanol, heptadecanol)    17 carbon atoms        C17H36O
Stearyl alcohol (1-octadecanol)    18 carbon atoms        C18H38O
Oleyl alcohol (1-octadecenol)    18 carbon atoms    unsaturated    C18H36O
Nonadecyl alcohol (1-nonadecanol)    19 carbon atoms        C19H40O
Arachidyl alcohol (1-eicosanol)    20 carbon atoms        C20H42O
Heneicosyl alcohol (1-heneicosanol)    21 carbon atoms        C21H44O
Behenyl alcohol (1-docosanol)    22 carbon atoms        C22H46O
Erucyl alcohol (cis-13-docosen-1-ol)    22 carbon atoms    unsaturated    C22H44O
Lignoceryl alcohol (1-tetracosanol)    24 carbon atoms        C24H50O
Ceryl alcohol (1-hexacosanol)    26 carbon atoms        C26H54O
1-Heptacosanol    27 carbon atoms        C27H56O
Montanyl alcohol, cluytyl alcohol, or 1-octacosanol    28 carbon atoms        C28H58O
1-Nonacosanol    29 carbon atoms        C29H60O
Myricyl alcohol, melissyl alcohol, or 1-triacontanol    30 carbon atoms        C30H62O
1-Dotriacontanol (Lacceryl alcohol)    32 carbon atoms        C32H66O
Geddyl alcohol (1-tetratriacontanol)    34 carbon atoms        C34H70O


 

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