Tridecanedioic acid is a family of organic compounds with a chemical formula of HOOC(CH2)10COOH.
The esters of Tridecanedioic acid are used as low-temperature plasticizers in polyvinyl chloride.
Moreover, esters of Tridecanedioic acid are used as lubricants which are used at a wide range of temperatures and are extensively utilized to manufacture synthetic musk.
CAS Number: 505-52-2
EC number: 208-011-4
Chemical formula: C₁₃H₂₄O₄
Molar mass: 244.167±0 dalton
Synonyms: TRIDECANEDIOIC ACID, 505-52-2, 1,11-Undecanedicarboxylic acid, Brassylic acid, Brassilic acid, 1,13-Tridecanedioic acid, UNII-PL3IQ40C34, PL3IQ40C34, CHEBI:73718, Undecane-1,11-dicarboxylic acid, NSC9498, DSSTox_CID_1683, DSSTox_RID_76281, DSSTox_GSID_21683, Brassylate, CAS-505-52-2, tridecanedioate, Brassilate, 1,11-Undecanedicarboxylicacid, NSC 9498, EINECS 208-011-4, 1,13-Tridecanedioate, 1,13-Brassylic Acid, AI3-18168, EC 208-011-4, 1,11-Undecanedicarboxylate, SCHEMBL20802, Undecane-1,11-dicarboxylate, CHEMBL3187746, DTXSID9021683, 1, 11-Undecanedicarboxylic acid, NSC-9498, ZINC1700020, Tox21_201301, Tox21_302982, LMFA01170014, MFCD00002740, s6063, STK033041, AKOS005381208, 1,11-Undecanedicarboxylic acid, 94%, MCULE-8192564811, NCGC00249020-01, NCGC00249020-02, NCGC00256463-01, NCGC00258853-01, AS-14882, M986, DB-121159, HY-128421, CS-0099256, FT-0606050, T0021, AB01332661-02, 505T522, Q2099072, 1,11-Undecanedicarboxylic acid, 208-011-4, 505-52-2, Acide tridécanedioïque, Brassylic acid, MFCD00002740, Tridecandisäure, Tridecanedioic acid, Undecane-1,11-dicarboxylic acid, 1,11-Undecanedicarboxylate, 1,13-Tridecanedioate, Brassilate, Brassylate, Tridecanedioate, Undecane-1,11-dicarboxylate, 1,11-Undecanedicarboxylicacid, 1 11-undecanedicarboxylic acid, 1, 11-Undecanedicarboxylic acid, 1,11-undecanedicarboxylic acid 98%, 1,11-undecanedicarboxylicacid, 1,13-Tridecanedioic acid, 638-53-9, Brassilic acid, EINECS 208-011-4, QA-7398, STK033041, tridecanedioic acid, ??? 95.0%, Tridecanedioicacid, Tridecanoic acid, undecane-1,11-dicarboxylic acid, 95%
Tridecanedioic acid is a chemical compound used in a wide range of applications through different industries.
Tridecanedioic acid, when found in the form of a flake or white powder, comes from the family of organic compounds called as dibasic acids.
Another name for dibasic acids is long-chain dicarboxylic acids.
The chemical formula of long-chain dicarboxylic acids is HOOC(CH2)11COOH.
Application of Tridecanedioic acids has been recommended by experts in the field of chemistry, for use in hot melt adhesives, high-performance nylon, high-performance polyamides, and many other applications.
Tridecanedioic acid is primarily used for the synthesis of fragrances and is a potential alternative for polycyclic acid as Tridecanedioic acid is an easily degradable chemical compound.
To overcome these challenges, Tridecanedioic acid is used for the synthesis of macrocyclic musk i.e. fragrances.
Tridecanedioic acid comes from the family of long-chain dicarboxylic acids.
Tridecanedioic acid is naturally occurring in animal tissues and plants.
When13 carbon molecules, 24 hydrogen molecules and 4 oxygen molecules come together, they form Tridecanedioic acid.
Tridecanedioic acids chemical formula is C13H24O4.
Tridecanedioic acid like most other Dicarboxyl acids can produce two kinds of salts because Tridecanedioic acid contains two carboxylic groups.
Tridecanedioic acid is a white crystalline substance, slightly soluble in water, and has a melting point of 130 ° C.
Tridecanedioic acid is used in polymers, biological solvents, lubricants, and perfumeries plasticizer production.
Tridecanedioic acid is used to manufacture plastics such as nylon-1313 as an intermediate.
Multi-pound production of nylon-1313 demonstrates that there are no serious obstacles to commercial production of this long-chain polyamide.
The synthesis of nylon-1313 is remarkably simple and straightforward when compared to the reactions required to produce nylon-11 and -12.
In many ways nylon-1313 is comparable to these other nylons, but Tridecanedioic acid is lower melting, slightly less dense, and more hydrophobic than either of Tridecanedioic acids counterparts.
This engineering resin can be produced economically using Tridecanedioic acid derived from crambe or other high-erucic acid oils.
Tridecanedioic acid is a family of organic compounds with a chemical formula of HOOC(CH2)10COOH.
Tridecanedioic acid is a versatile chemical intermediate.
Tridecanedioic acids were first created in the nineteenth century by oxidative ozonolysis of erucic acid.
Tridecanedioic acid is a dibasic acid, which is available in the market in the form of flakes, powder or in diluted form.
Tridecanedioic acid belongs to the family of organic compounds called long-chain dicarboxylic acid.
The esters of Tridecanedioic acid are used as low-temperature plasticizers in polyvinyl chloride.
Moreover, esters of Tridecanedioic acid are used as lubricants which are used at a wide range of temperatures and are extensively utilized to manufacture synthetic musk.
Commercially, Tridecanedioic acid serves as a monomer of dicarboxylic acid for the production of polyamides such as nylon 613 and nylon 1313.
The demand for Tridecanedioic acid is expected to increase over the forecast period, owing to rising applications of Tridecanedioic acid in various end-use industries such as fragrances & perfumes, lubricants, and adhesives coupled with important use in the formation of polyurethanes, alkyd resins, and polyamides.
Moreover, Tridecanedioic acid is used as monomers for certain co-polymers such as nylon 13,13.
Various diesters of Tridecanedioic acid are incorporated into PVC and are used as plasticizers.
These derivatives of Tridecanedioic acid possess property to remain stable at low temperature conditions.
Moreover, nylon that is manufactured with Tridecanedioic acid have low moisture absorption capability, which are suitable for applications that require toughness, retention of strength, abrasion resistance and electrical properties under changing climatic conditions.
Furthermore, the properties of nylon 1313 which is manufactured using Tridecanedioic acid is similar to that of the commercially produced polyamides such as nylon 11, 12, 610, and 612.
These factors are expected to drive demand for Tridecanedioic acid over the forecast period.
Tridecanedioic acid is majorly used in fragrance industry for synthesis of macrocyclic musk, however, other musk compounds such as nitro musk and polycyclic musk compounds are readily available in the market.
Moreover, direct contact with Tridecanedioic acid can cause skin & eye irritation and is expected to cause respiratory problems.
Availability of substitutes and Tridecanedioic acids potential to cause health problems are expected to hamper growth of the market over the forecast period.
Polymeric composition comprising a polyolefin and a diacid-diol aliphatic-aromatic copolyester with aromatic part consisting mainly of terephthalic acid or Tridecanedioic acids derivatives, aliphatic part consisting of azelaic acid, sebacic acid and Tridecanedioic acid and diol c2-c13.
The present invention relates to aliphatic-aromatic polyesters comprising: i) 40 to 60 mol %, based on components i to ii, of one or more dicarboxylic acid derivatives selected from the group consisting of: sebacic acid, azelaic acid and Tridecanedioic acid.
Tridecanedioic acid, when found in the form of a flake or white powder, comes from the family of organic compounds called as dibasic acids.
Another name for dibasic acids is long-chain dicarboxylic acids.
There are almost infinite esters obtained from carboxylic acids.
Esters are formed by removal of water from an acid and an alcohol.
Carboxylic acid esters are used as in a variety of direct and indirect applications.
Lower chain esters are used as flavouring base materials, plasticizers, solvent carriers and coupling agents.
Higher chain compounds are used as components in metalworking fluids, surfactants, lubricants, detergents, oiling agents, emulsifiers, wetting agents textile treatments and emollients.
They are also used as intermediates for the manufacture of a variety of target compounds.
The almost infinite esters provide a wide range of viscosity, specific gravity, vapor pressure, boiling point, and other physical and chemical properties for the proper application selections.
Tridecanedioic acid is mainly used in top-grade essence, perfume and artificial musk-T, packing materials for foodstuff, also is the important materials for nylon 1313, Polycyclic Synthetic Musks, Polyamide Resin, and Hot Melt Adhesive.
In addition, the important characteristics of Tridecanedioic acid like high solubility in water, strength, high resistance, etc. are also expected to boost the market growth by 2030.
Shifting preferences from polycyclic acid to Tridecanedioic acid for perfume manufacturing is the major factor predicted to create abundant growth opportunities for the global Tridecanedioic acid market during the forecast period.
Moreover, Tridecanedioic acid is also used as lubricants and adhesives for machine joints for smooth functioning.
And with the growing expansion of the automobile industry, the global Tridecanedioic acid market is also projected to witness immense growth opportunities by 2030.
Sky-rocketing cost of Tridecanedioic acid is the prime factor anticipated to hinder the market growth.
The growth and development of the perfume and fragrance industry, emerging market of Tridecanedioic acid along with Tridecanedioic acids applications like PVC and plasticizers clubbed with the use of the regenerating feedstocks, is expected to increase market growth in Tridecanedioic acid significantly.
Advanced technical applications of Tridecanedioic acid are expected to create lucrative opportunities in the lubricant industry, adhesive industry, and plastics industry.
That being said, the adverse effects of Tridecanedioic acid and the substitutes available in the market for consumers are likely to hinder the exponential rise of the Tridecanedioic acid market.
The global production of Tridecanedioic acid for perfumes is currently higher than any other acid and is expected to be the same for the coming years.
Nevertheless, other forms of musk compounds are available for use in the market, including nitro musk compounds and polycyclic musk compounds.
Tridecanedioic acid is predicted that this competition will be the central issue that will restrain market growth.
Because of the increased availability of sources of renewable raw materials like vegetable oil, Tridecanedioic acid consumption is the highest in Europe.
According to a report by Research Dive, Europe is currently the highest contributor to cash flow among all the regions studied and is anticipated to keep up Tridecanedioic acids dominance and lead over the projected timeline, accompanied by the Asia Pacific and North America.
Uses of Tridecanedioic acid:
Tridecanedioic acid is used in the production of high-grade flavors, fragrances and artificial musk-T, hot melt adhesives and engineering plastics, high-grade food packaging materials, and the main raw material of high-grade nylon 1313
Material of high-level essence, perfume and synthetic musk T; high grade food packing material; main material of high grade nylon 1313
Tridecanedioic acid is a dicarboxylic acid with 13 carbon atoms, occurring in plant and animal tissues.
Tridecanedioic acid exhibits typical carboxyl group chemistry useful in a variety of industrial applications.
Dicarboxylic acid can yield two kinds of salts, as they contain two carboxyl groups in Tridecanedioic acids molecules.
Tridecanedioic acid is a white crystalline; melting point at 130 C, slightly soluble in water.
Tridecanedioic acid is used in manufacturing plasticizer for polymers, biodegradable solvents, lubricants and perfumeries.
Tridecanedioic acid is used as an intermediates to produce engineering plastics such as nylon-1313
Dicarboxylic acid is a compound containing two carboxylic acid, -COOH, groups.
Straight chain examples are shown in table.
The general formula is HOOC(CH2)nCOOH, where oxalic acid's n is 0, n=1 for malonic acid, n=2 for succinic acid, n=3 for glutaric acid, and etc.
In substitutive nomenclature, their names are formed by adding -dioic' as a suffix to the name of the parent compound.
They can yield two kinds of salts, as they contain two carboxyl groups in Tridecanedioic acids molecules.
The range of carbon chain lengths is from 2, but the longer than C 24 is very rare.
The term long chain refers to C 12 up to C 24 commonly.
Carboxylic acids have industrial application directly or indirectly through acid halides, esters, salts, and anhydride forms, polymerization, and etc.
Dicarboxylic acids can yield two kinds of salts or esters, as they contain two carboxyl groups in one molecule.
Tridecanedioic acid is useful in a variety of industrial applications include;
Tridecanedioic acid is used in the synthesis of polycyclic synthetic musk, polyamide resins, hot melt adhesive.
Uses include:
Flexibilizer for nylon engineering plastics and fibers,
polyester films and adhesives,
urethane elastomers and elastomeric fibers,
lubricant basestocks and greases,
polyester and polyamide fibers,
wire-coating,
molding resins,
polyamide hot melts
Other Uses:
Plasticizer for polymers
Biodegradable solvents and lubricants
Engineering plastics
Epoxy curing agent
Adhesive and powder coating
Corrosion inhibitor
Perfumery and pharmaceutical
Electrolyte
Applications of Tridecanedioic acid:
Tridecanedioic acid is very useful in a wide variety of industrial applications, some of the uses of Tridecanedioic acid are listed below:
Plasticizer for polymers
Engineering plastics
Adhesive and powder coating
Perfumery and pharmaceutical
Biodegradable solvents and lubricants
Epoxy curing agent
Corrosion inhibitor
Electrolyte
Occurrence of Tridecanedioic acid:
Tridecanedioic acid was first obtained by oxidation of castor oil (ricinoleic acid) with nitric acid.
Tridecanedioic acid is now produced industrially by oxidation of cyclohexanol or cyclohexane, mainly for the production of Nylon 6-6.
Tridecanedioic acid has several other industrial uses in the production of adhesives, plasticizers, gelatinizing agents, hydraulic fluids, lubricants, emollients, polyurethane foams, leather tanning, urethane and also as an acidulant in foods.
Tridecanedioic acid was detected among products of rancid fats.
Tridecanedioic acids origin explains for Tridecanedioic acids presence in poorly preserved samples of linseed oil and in specimens of ointment removed from Egyptian tombs 5000 years old.
Tridecanedioic acid displays bacteriostatic and bactericidal properties against a variety of aerobic and anaerobic micro-organisms present on acne-bearing skin.
Tridecanedioic acid is produced industrially by alkali fission of castor oil.
Sebacic acid and Tridecanedioic acids derivatives have a variety of industrial uses as plasticizers, lubricants, diffusion pump oils, cosmetics, candles, etc.
Tridecanedioic acid is also used in the synthesis of polyamide, as nylon, and of alkyd resins.
Tridecanedioic acid can be produced from erucic acid by ozonolysis, but also by microorganisms (Candida sp.) from tridecane.
Tridecanedioic acid is now produced by fermentation of long-chain alkanes with a specific strain of Candida tropicalis.
Tridecanedioic acid was shown that hyperthermophilic microorganisms specifically contained a large variety of dicarboxylic acids.
Tridecanedioic acid was discovered that these compounds appeared in urine after administration of tricaprin and triundecylin.
Although the significance of their biosynthesis remains poorly understood, Tridecanedioic acid was demonstrated that ω-oxidation occurs in rat liver but at a low rate, needs oxygen, NADPH and cytochrome P450.
Tridecanedioic acid was later shown that this reaction is more important in starving or diabetic animals where 15% of palmitic acid is subjected to ω-oxidation and then tob-oxidation, this generates malonyl-coA which is further used in saturated fatty acid synthesis.
Copolyamides derived from Tridecanedioic acid:
Polyamides were prepared from C6 to C12 diamines with Tridecanedioic acid, a linear C13 dicarboxylic acid, derived from Crambe seed oil.
One distinct characteristic of these polymers is their low moisture adsorption as compared to nylon 66 and nylon 6.
To modify the properties of these nylons, multi-component copolyamides were prepared from hexamethylene diamine and mixtures of Tridecanedioic acid with adipic, terephthalic, or isophthalic acids.
Tridecanedioic acid was found that the melting points of the co-polyamides were changed by the choice and the levels of the diacids used.
The melting point-composition curves all show a eutectic minimum.
They will be commercially viable when Tridecanedioic acid becomes available on a large scale and is competitively priced.
Tridecanedioic acid, a dicarboxylic acid with the molecular formula - HOOC(CH2)11COOH - is a fatty acid which can be technically extracted from erucic acid together with pelargonic acid.
The compounds of the Tridecanedioic acids are used in the food and cosmetic industry.
This refers e.g. to ethylene brassylate, an ethylene glycol diester of brassy acid.
The dimethyl ester of brassyl acid(dimethyl brassylate) is used in cosmetic formulations as skin care products and emollients.
Tridecanedioic acid is detected as an excessive fatty acid in addition to phytic acid (Zellweger syndrome) and cerotic acid (adrenoleukodystrophy) as pathological excretion products in the urine of children with congenital adrenoleukodystrophy or Zellweger syndrome.
Estimation of Tridecanedioic acid by gas chromatography-mass spectrometry:
The main focus of this work is to estimate Tridecanedioic acid (BA) using gas chromatography-mass spectrometry (GC-MS).
Tridecanedioic acid is a product obtained from the oxidative cleavage of Erucic Acid (EA).
Tridecanedioic acid has various applications for making nylons and high performance polymers.
Tridecanedioic acid is a 13 carbon compound with two carboxylic acid functional groups at the terminal end.
Tridecanedioic acid has a long hydrocarbon chain that makes the molecule less sensitive to some of the characterization techniques.
Tridecanedioic acid is chemical formed from processing erucic oils.
Chemical processing method is often used because of Tridecanedioic acids low cost and easy to follow for the production of Tridecanedioic acid.
The increase in the use of Tridecanedioic acid in the manufacture of perfumes, combined with an rise in the use of renewable sources, such as low-priced and readily available vegetable oil, is expected to drive the growth of the Tridecanedioic acid industry.
The rise the use of Tridecanedioic acid in the manufacture of perfumes is related to Tridecanedioic acids desirable attributes, including such diffusivity, and beneficial content, thus driving market growth.
However, the negative impacts of Tridecanedioic acid and the accessibility of alternatives are anticipated to hamper the growth of the global market for Tridecanedioic acid.
Based on product type, the market for global Tridecanedioic acid is further segmented into paraffin oil and vegetable oil.
Based on process, the market for global Tridecanedioic acid is further segmented into chemical, and fermentation.
Based on application, the market for global Tridecanedioic acid is further segmented fragrances, adhesives, plastics, lubricants, and other.
In terms of Geography, the global Tridecanedioic acid market has been segmented into North America, Europe, Asia Pacific, Latin America, and Middle East & Africa.
The Asia-Pacific region dominates the global market for Tridecanedioic acid.
As a result of rapid urbanization and an increase in disposable income along with change in people's lifestyle, the use of Tridecanedioic acid in industrial businesses, such as perfume production, has increased.
North America has a large market share.
Tridecanedioic acid holds one of the world 's strong pharma bases.
Improved investment in the phrmaceutical industry and growing people's spending power have contributed to a boom in the North American market for Tridecanedioic acid.
Countries such as France, Italy and Spain are the center of the fragrance industry and have the best perfumes produced in the world.
Such a strong manufacturing base and sustainability in Europe has caused a spike in the demand for perfumes due to the evolving lifestyle of the peiople and has caused an increase in the market for Tridecanedioic acid.
The Middle East and Africa are expected to face substantial growth.
Due to the fact that the processing of Tridecanedioic acid is less tedious compared to fermentation, many producers in the region have experienced an increase in market growth.
Latin America is experiencing relatively slow growth due to the limited number of manufacturers and the availability of substitutes.
Manufacturing Methods of Tridecanedioic acid:
The U.S. Emery Company used special rapeseed oil to extract erucic acid, which was then decomposed by ozone oxidation.
Japanese mining companies use self-produced straight-chain alkanes as raw materials for fermentation production.
In addition, in addition to linear alkanes, the raw materials can also be synthesized from linear alkenes, saturated or unsaturated fatty acids, hexadecanoates and the like.
Handling and Storage of Tridecanedioic acid:
Storage:
Keep container closed when not in use.
Store in a tightly closed container.
Store in a cool, dry, well-ventilated area away from incompatible substances.
Store the container tightly closed in a dry, cool and well-ventilated place.
Store apart from foodstuff containers or incompatible materials.
Suggested storage:
Store in cool, dry, well-ventilated area away from incompat.
Handling:
Wash thoroughly after handling.
Remove contaminated clothing and wash before reuse.
Minimize dust generation and accumulation.
Avoid contact with eyes, skin, and clothing.
Keep container tightly closed.
Avoid ingestion and inhalation.
Use with adequate ventilation.
Handling in a well ventilated place.
Wear suitable protective clothing.
Avoid contact with skin and eyes.
Avoid formation of dust and aerosols.
Use non-sparking tools.
Prevent fire caused by electrostatic discharge steam.
First Aid Measures of Tridecanedioic acid:
Ingestion:
Never give anything by mouth to an unconscious person.
Get medical aid.
Do NOT induce vomiting.
If conscious and alert, rinse mouth and drink 2-4 cupfuls of milk or water.
Inhalation:
Remove from exposure to fresh air immediately.
If breathing is difficult, give oxygen.
Get medical aid.
DO NOT use mouth-to-mouth respiration.
If breathing has ceased apply artificial respiration using oxygen and a suitable mechanical device such as a bag and a mask.
Skin:
Get medical aid.
Flush skin with plenty of soap and water for at least 15 minutes while removing contaminated clothing and shoes.
Wash clothing before reuse.
Eyes:
Immediately flush eyes with plenty of water for at least 15 minutes, occasionally lifting the upper and lower eyelids.
Get medical aid.
Fire Fighting Measures of Tridecanedioic acid:
Wear a self-contained breathing apparatus in pressure-demand, MSHA/NIOSH (approved or equivalent), and full protective gear.
During a fire, irritating and highly toxic gases may be generated by thermal decomposition or combustion.
Runoff from fire control or dilution water may cause pollution.
To extinguish fire, use water, dry chemical, chemical foam, or alcohol-resistant foam.
Use agent most appropriate to extinguish fire.
Identifiers of Tridecanedioic acid:
InChI: InChI=1S/C13H24O4/c14-12(15)10-8-6-4-2-1-3-5-7-9-11-13(16)17/h1-11H2,(H,14,15)(H,16,17)
InChIKey
DXNCZXXFRKPEPY-UHFFFAOYSA-N
CAS Registry Number: 505-52-2
Reaxys registry number: 1786404
ChEBI ID: 73718
mapping relation type: exact match
ChEMBL ID: CHEMBL3187746
SPLASH: splash10-0089-4980000000-e0f9e32666a9f5b5a8fa
splash10-0006-0090000000-38331eb24eac374bd304
ZVG number: 104435
DSSTox substance ID: DTXSID9021683
DSSTOX compound identifier: DTXCID901683
NSC number: 9498
EC number: 208-011-4
UNII: PL3IQ40C34
LIPID MAPS ID: LMFA01170014
instance of: chemical compound
dicarboxylic acid
fatty acid
chemical structure
mass: 244.167±0 dalton
chemical formula: C₁₃H₂₄O₄
canonical SMILES: C(CCCCCC(=O)O)CCCCCC(=O)O
found in taxon: Trypanosoma brucei
Properties of Tridecanedioic acid:
PSA:74.6
XLogP3:3.7
Appearance:Solid
Density:1.1±0.1 g/cm3
Melting Point:111 °C
Boiling Point:215-217 °C @ Press: 2 Torr
Flash Point:223.5±17.7 °C
Refractive Index:1.475
Water Solubility:H2O: Insoluble
Storage Conditions:Store below +30°C.
Chemical and Physical Properties of Tridecanedioic acid:
Molecular Weight: 244.33
XLogP3: 3.7
Hydrogen Bond Donor Count: 2
Hydrogen Bond Acceptor Count: 4
Rotatable Bond Count: 12
Exact Mass: 244.16745924
Monoisotopic Mass: 244.16745924
Topological Polar Surface Area: 74.6 Ų
Heavy Atom Count: 17
Complexity: 192
Isotope Atom Count: 0
Defined Atom Stereocenter Count: 0
Undefined Atom Stereocenter Count: 0
Defined Bond Stereocenter Count: 0
Undefined Bond Stereocenter Count: 0
Covalently-Bonded Unit Count: 1
Compound Is Canonicalized: Yes
Specifications of Tridecanedioic acid:
MOLECULAR WEIGHT: 244.33
EINECS: 208-011-4
SMILES: C(CCCCCCCCCCCC(O)=O)(O)=O
INCHI: 1S/C13H24O4/c14-12(15)10-8-6-4-2-1-3-5-7-9-11-13(16)17/h1-11H2,(H,14,15)(H,16,17)
INCHIKEY: DXNCZXXFRKPEPY-UHFFFAOYSA-N
WATER SOLUBILITY: 1500 mg/L
MELTING POINT: 111 ° C
ATMOSPHERIC OH RATE CONSTANT: 1.55E-11 cm3/molecule-sec
LOG P (OCTANOL-WATER): 3.670
MELTING POINT: 112-114 °C
WATER SOLUBILITY: Insoluble
Keywords of Tridecanedioic acid:
Carbon Compounds
Carboxylic Acids
Chains
Cleavage
Functionals
Hydrocarbons
Nonanoic Acid
Performance
Polymers
Spectroscopy
Synthesis
Related Products of Tridecanedioic acid:
Diethyl (Acetylamino)(2-phenylethyl)malonate
4'-Deoxy Vincristine Sulfate (>75%)
1-[(3,4-Dimethoxyphenyl)methyl]-3,4-dihydro-6,7-dimethoxy-2(1H)-isoquinolinepropanoic Acid
1-(((2,6-dimethylpyrimidin-4-yl)oxy)methyl)cyclopropane-1-carbaldehyde
1-(((4,6-dimethylpyrimidin-2-yl)oxy)methyl)cyclopropane-1-carbaldehyde
MeSH of Tridecanedioic acid:
Brassylic acid
Undecanedicarboxylic acid
tridecanedioic acid
tridecanedioic acid, disodium salt
tridecanedioic acid, monosodium salt