PROPYLENE CARBONATE

Propylene Carbonate is a clear and odourless liquid used primarily as a polar aprotic solvent.  Propylene Carbonate is a clear, Low odor and VOC-exempt solvent that can be used in a variety of cleaning and industrial applications. From cosmetics to paint strippers this versatile solvent is found in many industrial and consumer applications. 
Propylene Carbonate finds many diverse uses as a solvent. 
 

For example:

In Industrial coatings and Decorative coatings, as well as in Inks, it can be used to trigger and improve the effectiveness of the viscosity modifiers used.
In Metal Treatment it can be used to formulate effective surface cleaners and degreasers.
Further applications are found in Polyurethanes, Adhesives and Sealants as well as agricultural and cosmetic formulations. 
Propylene Carbonate also finds applications in lithium battery manufacturing.

Propylene Carbonate is a VOC exempt solvent that is primarily used in paint strippers, surface cleaners, and degreasers. 
It can also be used in paints and coatings as a replacement for the recently banned PCBTF.

What is Propylene Carbonate?
Propylene Carbonate is a clear and odourless liquid used primarily as a polar aprotic solvent. 
Usually being produced by the carbonation of an epoxide, Propylene Carbonate is seen as a green solvent, using up CO2 in its production. 
Its high boiling point and flash point make this a relatively safe solvent that is not classified as a VOC in the US.

CAS NO: 108-32-7
PROPYLENE CARBONATE
EINECS NO.: 203-572-1
FORMULA: C4H6O3
MOL WT.: 102.09
SYNONYMS: 4-methyl-1,3-Dioxolan-2-one; 1,2-Propylene Carbonate; 1,2-Propanediol cyclic carbonate; PC; Carbonic Acid Cyclic Propylene Ester;

Ideal for baked coatings and other slow solvent release applications
Reactive diluent for coatings
Excellent nail polish remover
Excellent binder for foundry sand molds
Gelling agent for clay
High boiling point solvent
Low evaporation rate solvent
EPA VOC exempt solvent
Readily Biodegradable
Low odor


Propylene Carbonate is a low VOC solvent derived from propylene glycol.

Propylene carbonate is used in a variety of syntheses and applications as a polar, aprotic solvent. 
Propylene carbonate can also be found in some adhesives, paint strippers, cosmetics, and can be used as a plasticizer.


The increasing demand for propylene carbonate in the manufacturing of lithium-ion batteries as well as in the paint & coatings industries is expected to fuel the demand of the global propylene carbonate market

The surging demand for electric vehicles to enhance environmental sustainability is expected to propel the demand for lithium-ion batteries in electric cars, trucks, buses, and two-wheelers and thus, boost the demand for polypropylene carbonate. 
In addition, the rise in oil & gas exploration activities is positively influencing the application of propylene carbonate usage in the oil and gas separation process.
Furthermore, the development of organic-based beauty and personal care products and the emergence of Asia-based EV battery manufacturers in Europe are factors projected to create lucrative opportunities for the producers of propylene carbonate
Propylene carbonate (PC) is an organic compound with the formula CH3C2H3O2CO. It is a carbonate ester derived from propylene glycol. This colorless and odorless liquid is useful as a polar, aprotic solvent

Propylene Carbonate is a low VOC solvent derived from propylene glycol.

Propylene carbonate is used in a variety of syntheses and applications as a polar, aprotic solvent. 
Propylene carbonate can also be found in some adhesives, paint strippers, cosmetics, and can be used as a plasticizer.


Propylene carbonate acts as a solvent and viscosity reducer in coatings. 
Propylene carbonate has high boiling and flash points, a low order of toxicity as well as a mild ether-like odor. 
Propylene carbonate is stable under most conditions and is not hydroscopic or corrosive. 
Propylene carbonate is particularly well suited for applications requiring a water white product or high purity. 
Examples would be electronics or where recycling of spent material will occur.

Propylene carbonate is an odorless and colorless organic compound derived from propylene glycol. 
Propylene carbonate has a very high boiling point and is also extremely soluble in water, often being used to dissolve other substances. 
Propylene carbonate is widely used in the cosmetics industry, and is also used in a variety of decreasing and cleaning applications. 
Propylene carbonate has various other uses as well, including being used as a plasticizer, an additive to increase the fluid properties of a material. 
Propylene carbonate is used in inks for various applications, as well as ink cleaners, and in cleaning solutions for carburetors, unsaturated polyester, and for cleaning circuit boards and other electronic parts. 
Propylene carbonate is often used instead of other more volatile and harmful cleaning solvents, because it is not considered to be as volatile as many others. 
Propylene carbonate is compatible with other solvents, making it versatile and effective at reducing surface tension.

Propylene Carbonate is commonly used in many applications such as:
Cleaners; Degreasers; Paints; Coatings; Inks; Paint Stripper; Nail Polish Remover; Plasticizers; Cosmetics; Adhesives; Lithium Battery Electrolyte Components

Propylene carbonate is an colorless and odorless liquid. It is chiral but is used exclusively as a racemic mixture. 
It is useful as a polar aprotic solvent and synthetic material.

Propylene carbonate
CAS Number:
108-32-7
Synonyms:
4-Methyl-1,3-dioxolan-2-one; 1,2-Propylene carbonate; 1,2-Propanediol cyclic carbonate; Propylene glycol cyclic carbonate.

Are you looking for a chemical with low toxicity, low evaporation rate, and VOCs exemption? Propylene Carbonate has all of those characteristics and it is suitable for a variety of applications. It can be used for painting, coating, as a cleaning agent, and as solvent for many other industries.

Benefits of Propylene Carbonate
Not only it has a low evaporation rate, low toxicity, and VOC exemption, Propylene Carbonate also has other benefits such as:

Improves lubricity
It is chemically stable
Co-firing in any atmosphere without oxidation
Excellent viscosity properties and green strength
Propylene Carbonate is one of the most eco-efficient alternatives for coating wires.
Applications of Propylene Carbonate as a Cleaning Agent
Ink cleaner
All purpose industrial and consumer cleaners
Electronic cleaners
Unsaturated polyester clean up
Metal cleaner
Degreaser


Applications of Propylene Carbonate in the Cosmetic Industry
Propylene Carbonate is not corrosive, therefore, it can use as a solvent for lipsticks, skin cleansing products, eye shadows, and mascaras. 
Propylene Carbonate  is suitable for this industry since it has the ability to dissolve substance and it is a colorless, odorless, and  it is a not corrosive liquid.

Another uses of Propylene Carbonate

Propylene Carbonate can be used to:

Remove CO2 from natural gas.
Increase electrolyte solubility/ionic conductivity, and decrease dioxide vapor pressure in lithium batteries.
As plasticizer
As an important intermediate in the synthesis of tenofovir.

Propylene Carbonate Uses
VOC Exempt Solvent – Propylene Carbonate (DMC) received its Federal VOC exemption on January 13, 2009. As of March 1, 2011 it is exempt in 42 States. (Last updated: 03.2011; please contacts us for the most up to date information on the VOC exemption state by state.)

Paints and Coatings – Propylene Carbonate can be used as VOC exempt solvent in paints and coatings as a tail solvent. PC is a slow evaporating polar solvent.

Cleaning Applications – Alone or combined with other solvents, Propylene Carbonate is effective as a hard surface cleaner, polymer/resin cleaner, fiberglass, polyester and polyurethane cleaner.

Reactive Intermediate – Propylene Carbonate can be used for derivative chemistries such as carbamate formation, hydroxyalkyation, transesterification and others

Chemical Name: Propylene Carbonate
Synonyms: 4-Methyl-1,3-dioxolan-2-one; Cyclic propylene carbonate; Carbonic acid propylene ester; Cyclic 1,2-propylene carbonate; Propylene glycol cyclic carbonate; 1,2-Propanediol carbonate; 4-Methyl-2-oxo-1,3-dioxolane
Chemical Formula: C4H6O3
CAS Number: 108-32-7
EC Number: 203-572-1

Propylene carbonates are important intermediates in a number of different processes, for instance, as the replacement of highly toxic phosgene as carbonylating agents in processes such as the production of isocyanates or polycarbonates.

Another important use of propylene carbonates is the production of 1,2-propanediol by catalyzed hydrolysis. The propylene carbonates can also be used for the preparation of dimethyl carbonate, which has raised interest for use as octane enhancers in fuels as a replacement for methyl tert-butyl ether.


Propylene Carbonate (PC) is a PU-plasticizer. It is VOC-free clear polar solvent having high boiling and flashpoints.
Propylene Carbonate (PC) is a carbonate ester derived from propylene glycol with the peculiarity to have a low order of toxicity and a mild ether-like odor.

Propylene Carbonate (PC) is stable under most conditions and it is not hydroscopic or corrosive.
It is particularly well suited for applications requiring a water-white product or high purity.
It can be used in cosmetics and personal care products; mainly in the formulation of make-up, primarily lipstick, eye shadow, and mascara, as well as in skin cleansing products.

Propylene Carbonate (PC) being a cyclic carbonate reacts with amines to form carbamates, undergoes hydroxy alkylation and transesterification can be used as an isocyanate and unsaturated polyester resin cleanup solvent, viscosity reducer in coatings, CO2 extraction solvent, electrolyte in lithium batteries, polar additive for clay gellants, foundry binder catalyst, and textile dye carrier and cleaner.
 


1, 3-Dioxolan-2-one, 4-methyl-
1,2-Propanediol cyclic carbonate
1,3-Dioxolan-2-one, 4-methyl- [ACD/Index Name]
107913
108-32-7 [RN]
4-Methyl-1,3-dioxol-2-one [ACD/IUPAC Name]
4-Methyl-1,3-dioxolan-2-on [German] [ACD/IUPAC Name]
4-Methyl-1,3-dioxolan-2-one [ACD/IUPAC Name]
4-Méthyl-1,3-dioxolan-2-one [French] [ACD/IUPAC Name]
4-Methyl-2-oxo-1,3-dioxolane
8D08K3S51E
Arconate 1000
Carbonic acid cyclic 1,2-propylene ester
Carbonic acid, cyclic propylene ether
Cyclic propylene carbonate
FF9650000
Jeffsol PC
MFCD00005385 [MDL number]
PC
PC-HP
Propylene carbonate [Wiki]
Propylene glycol cyclic carbonate
UNII:8D08K3S51E
(4S)-4-Methyl-1,3-dioxolan-2-one [ACD/IUPAC Name]
(R)-4-Methyl-1,3-dioxolan-2-one
(S)-4-Methyl-1,3-dioxolan-2-one
[108-32-7]
1,2-PDC
1,2-PROPANEDIOL CARBONATE
1,2-Propanediyl carbonate
1,2-PROPYLENE CARBONATE
1,2-Propylene glycol carbonate
1,2-Propylene-d6 Carbonate
1-Methylethylene carbonate
2-(Piperidin-4-yl)acetonitrile
202480-74-8 [RN]
2-Oxo-4-methyl-1,3-dioxolane
4-Methyl-1,3-dioxolan-2-one, Propylene glycol carbonate, Carbonic acid propylene glycol ester
4-METHYL-1,3-DIOXOLANE-2-ONE
Arconate 5000
Arconate propylene carbonate
Carbonic acid cyclic methylethylene ester
Carbonic acid, cyclic propylene ester
Carbonic acid, propylene ester
CYCLIC 1,2-PROPYLENE CARBONATE
Cyclic methylethylene carbonate
Dipropylene carbonate
http:////www.amadischem.com/proen/545632/
http:////www.amadischem.com/proen/592421/
MFCD00798264 [MDL number]
MFCD00798265 [MDL number]
Propylene Carbonate (Industrial Grade)
propylene carbonate [pc]
propylene carbonate 99%
propylene carbonate 99.5%
propylene carbonate, 99%
propylene carbonate, 99%,
propylene carbonate, 99.5%
propylene carbonate, 99.5%, anhydrous, acroseal??
Propylene carbonate, anhydrous, Water 50ppm Max.
propylene carbonate, reagent
propylene carbonate??? 99%, hydry, water???50 ppm (by k.f.)???
propylenecarbonate
Propylenester kyseliny uhlicite [Czech]
Propylenester kyseliny uhlicite
Solvenon PC
Texacar PC
WLN: T5OVOTJ D


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Synonyms: 1,2-Propanediol cyclic carbonate, 4-Methyl-1,3-dioxolan-2-one; CAS Number:108-32-7; Empirical Formula:C4H6O3; Molecular Weight:102.09 ; Beilstein/REAXYS Number:107913 
EC Number:203-572-1; MDL number MFCD00005385; PubChem Substance ID:57648504 

Other names: 4-Methyl-1,3-dioxolan-2-one; Propylene glycol carbonate; Carbonic acid propylene glycol ester ;1,3-Dioxolan-2-one, 4-methyl-; Carbonic acid, cyclic propylene ester; Cyclic methylethylene carbonate; Cyclic propylene carbonate; Cyclic 1,2-propylene carbonate; Propylene glycol cyclic carbonate; 1-Methylethylene carbonate; 1,2-Propanediol carbonate; 1,2-Propanediol cyclic carbonate; 1,2-Propanediyl carbonate; 1,2-Propylene carbonate; 4-Methyl-1,3-dioxolan-2-one; 1,2-Propylene glycol carbonate; 4-Methyl-1,3-dioxol-2-one; Dipropylene carbonate; 4-Methyldioxalone-2; 4-Methyl-2-oxo-1,3-dioxolane; 1,2-PDC; Propylenester kyseliny uhlicite; Arconate propylene carbonate; PC-HP; Solvenon PC; Texacar PC; Arconate 5000; Carbonic acid cyclic methylethylene ester; Carbonic acid, propylene ester; NSC 11784

Propylene carbonate (PC) is a polar aprotic substance with very similar physicochemical characteristics to the organic solvents traditionally used for organic synthesis, such as acetonitrile and acetone. 
Therefore, PC is beginning to be used as a “green” sustainable alternative solvent for chemical transformations. PC is a low toxicity, non-corrosive colourless liquid with a high boiling point and low vapour pressure. 
It is biodegradable and economical, allowing its large-scale use. PC can be prepared by a reaction between propylene epoxide and carbon dioxide with 100% atomic economy. The easy preparation of propylene epoxide and the use of an available, abundant, economical, and renewable source of carbon, such as CO2, make this process one of the best routes for the synthesis of PC. 
Therefore, we present in this review numerous catalytic systems that have been studied to improve the efficiency of this reaction. Certain interesting examples of reactions using PC are found in the literature, of which we discuss asymmetric hydrogenation, hydrosilylation, asymmetric aldol reactions, the asymmetric synthesis of cyanohydrins, the synthesis of heterocyclic compounds, such as bisindole and tetrahydroquinoline, the hydroacylation of alkynes, α-hydrazination reactions, oxidations, the Sonogashira reaction, allylic alkylation and asymmetric amination, the Heck reaction, enzymatic kinetic resolution, and isomerisation-hydroformylation reactions.

Keywords: Propylene carbonate, carbonic acid diesters, green chemistry, green solvent, organic synthesis, environment.

Use: Propylene Carbonate (PC) is a VOC-free clear polar solvent having high boiling and flash points. Propylene Carbonate (PC) is a carbonate ester derived from propylene glycol with the peculiarity to have a low order of toxicity and a mild ether-like odor. Propylene Carbonate (PC) is stable under most conditions and it is not hydroscopic or corrosive. It is particularly well suited for applications requiring a water white product or high purity. It can be used in cosmetics and personal care products; mainly in the formulation of make-up, primarily lipstick, eye shadow, and mascara, as well as in skin cleansing products.
Use: Propylene carbonate is used in a variety of syntheses and applications as a polar, aprotic solvent. It can also be found in some adhesives, paint strippers, cosmetics, and can be used as a plasticizer.

Description
General description
Propylene carbonate can be synthesized from propylene oxide and CO2. Optically active form of propylene carbonate can be prepared from the reaction between CO2 and racemic epoxides.
Decomposition of propylene carbonate on the graphite electrode in lithium batteries results in the formation of a lithium intercalated compound.

Propylene carbonate is a cyclic carbonate that is commonly used as a solvent and as a reactive intermediate in organic synthesis. 
It is being considered as a potential electrochemical solvent due to its low vapor pressure, high dielectric constant and high chemical stability.

Application
Propylene carbonate may be used as a solvent for the asymmetric hydrogenation of nonfunctionalized olefins.


Propylene carbonate (often abbreviated PC) is an organic compound with the formula C4H6O3. It is a cyclic carbonate ester derived from propylene glycol. 
This colorless and odorless liquid is useful as a polar, aprotic solvent.
Propylene carbonate is chiral, but is used exclusively as the racemic mixture in most contexts.


Preparation
Although many organic carbonates are produced using phosgene, propylene and ethylene carbonates are exceptions. 
They are mainly prepared by the carbonation of the epoxides (epoxypropane, or propylene oxide here):

CH3CHCH2O + CO2 → CH3C2H3O2CO
The process is particularly attractive since the production of these epoxides consumes carbon dioxide. Thus this reaction is a good example of a green process. 
The corresponding reaction of 1,2-propanediol with phosgene is complex, yielding not only propylene carbonate but also oligomeric products.

Propylene carbonate can also be synthesized from urea and propylene glycol over zinc acetate.

Applications
As a solvent
Propylene carbonate is used as a polar, aprotic solvent. It has a high molecular dipole moment (4.9 D), considerably higher than those of acetone (2.91 D) and ethyl acetate (1.78 D). 
It is possible, for example, to obtain potassium, sodium, and other alkali metals by electrolysis of their chlorides and other salts dissolved in propylene carbonate.

Due to its high dielectric constant of 64, it is frequently used as a high-permittivity component of electrolytes in lithium batteries, usually together with a low-viscosity solvent (e.g. dimethoxyethane). 
Its high polarity allows it to create an effective solvation shell around lithium ions, thereby creating a conductive electrolyte. 
However, it is not used in lithium-ion batteries due to its destructive effect on graphite.

Propylene carbonate can also be found in some adhesives, paint strippers, and in cosmetics. It is also used as plasticizer.
 Propylene carbonate is also used as a solvent for removal of CO2 from natural gas and synthesis gas where H2S is not also present.
This use was developed by El Paso Natural Gas Company and Fluor Corporation in the 1950s for use at the Terrell County Gas Plant in West Texas, now owned by Occidental Petroleum.

Other
Propylene carbonate product may be converted to other carbonate esters by transesterification as well (see Carbonate ester#Carbonate transesterification).

In electrospray ionization mass spectrometry, propylene carbonate is doped into low surface tension solutions to increase analyte charging.

In Grignard reaction propylene carbonate (or most other carbonate esters) might be used to create tertiary alcohols.

IUPAC name: 4-Methyl-1,3-dioxolan-2-one
Other names: (R,S)-4-Methyl-1,3-dioxolan-2-one; Cyclic propylene carbonate; Carbonic acid propylene ester; Cyclic 1,2-propylene carbonate; Propylene glycol cyclic carbonate;1,2-Propanediol carbonate
;4-Methyl-2-oxo-1,3-dioxolane; Arconate 5000; Texacar PC

CAS Number: 108-32-7 

Properties
Chemical formula: C4H6O3
Molar mass: 102.089 g·mol−1
Appearance: Colorless liquid
Density: 1.205 g/cm3
Melting point: −48.8 °C 
Boiling point: 242 °C 
Solubility in water: Very soluble (240 g/L at 20°C)
Refractive index (nD):1.4189
CAS number: 108-32-7
EC index number: 607-194-00-1
EC number: 203-572-1
Hill Formula: C₄H₆O₃
Molar Mass: 102.09 g/mol
HS Code: 2920 90 10

Physicochemical Information
Boiling point: 243 °C (1013 hPa)
Density: 1.20 g/cm3 (20 °C)
Explosion limit: 1.8 - 14.3 %(V)
Flash point: 123 °C
Ignition temperature: 435 °C
Melting Point: -49 °C
pH value: 7.0 (200 g/l, H₂O, 20 °C)
Vapor pressure: 0.04 hPa (20 °C)
Viscosity kinematic: 1.4 mm2/s (43 °C)
Solubility: 240 g/l
Toxicological Information
LD 50 oral: LD50 Rat > 5000 mg/kg
LD 50 dermal: LD50 Rabbit > 20000 mg/kg

INDUSTRIAL USES:
Adhesives and sealant chemicals
Component in Li-ion electrolyte
Intermediates
Ion exchange agents
Lubricants and lubricant additives
Paint
Paint additives and coating additives not described by other categories
Photosensitive chemicals
Plasticizers
Solvents (which become part of product formulation or mixture)

Methods of Manufacturing    
The most important and versatile method for producing carbonates is the phosgenation of hydroxy compounds. 
Over the past 20 years, the trend is to manufacture carbonates without the use of phosgene. 
This method has the advantage of avoiding the use of highly toxic phosgene as well as considerably lower cost. 
The catalytic insertion of CO2 with oxiranes directly provides the five-membered cyclic carbonate.
Oxiranes such as ethylene oxide and propylene oxide undergo insertion at ~150-175 °C under pressure with the aid of a quaternary ammonium salt catalyst to yield ethylene carbonate and propylene carbonate, respectively.


Propylene carbonate dipolar aprotic solvent is a next-generation, high performing solvent. 
Propylene carbonate works well in a variety of different applications thanks to its excellent solvency power and water miscibility. It is a safer alternative to commonly used dipolar aprotic solvents like NMP (N-methylpyrrolidone), DMAc (dimethylacetamide), DMSO (dimethylsulfoxide), DMF (dimethylformamide), and acetonitrile, some of which face increasing regulatory pressure.

Key Benefits
Excellent performance in various applications
Excellent NMP and NEP replacement
Favorable safety, health, and environmental profile


Polyurethane dispersion (PUD) coating

Propylene carbonate is a high performance, safer cosolvent for water-based polyurethanes. Effective as both a solvent and coalescent for the PUD market, 
Propylene carbonate can also be an effective NMP replacement. It can provide not only formulation flexibility but also a favorable safety, health, and environmental profile. 
Propylene Carbonte is a high performance, safer cosolvent for water-based polyurethanes. Effective as both a solvent and coalescent for the PUD market 

Cleaners and paint strippers
When employed in cleaners and paint strippers, Propylene Carbonate has demonstrated to be an effective NMP replacement. 
The high solvency power can enhance performance of industrial cleaning formulations. Propylene Carbonate can be used for cleaning molds or tools related to polyurethane foam, polymer, polyester, or epoxy resins. 
The lower volatility of Propylene Carbonate is beneficial for reduced worker and environmental exposure.


Pharmaceutical synthesis
Propylene carbonate can be considered for use as a medium to carry out various chemical reactions, such as the production of pharmaceuticals. In such applications, it can be a replacement for solvents like NMP, NEP, DMF, and DMAc.


Safety
Clinical studies indicate that propylene carbonate does not cause skin irritation or sensitization when used in cosmetic preparations, whereas moderate skin irritation is observed when used undiluted. 
No significant toxic effects were observed in rats fed propylene carbonate, exposed to the vapor, or exposed to the undiluted liquid.
In the US, propylene carbonate is not regulated as a volatile organic compound (VOC) because it does not contribute significantly to the formation of smog and because its vapor is not known or suspected to cause cancer or other toxic effects.

PROPYLENE CARBONATE
108-32-7
4-Methyl-1,3-dioxolan-2-one
1,2-Propylene carbonate
1,2-Propanediol cyclic carbonate
1,3-Dioxolan-2-one, 4-methyl-
Cyclic propylene carbonate
Texacar PC
Arconate 5000
1,2-Propanediol carbonate
1-Methylethylene carbonate
Cyclic 1,2-propylene carbonate
Dipropylene carbonate
1,2-Propanediyl carbonate
4-Methyldioxalone-2
Propylene glycol cyclic carbonate
Cyclic methylethylene carbonate
4-Methyl-2-oxo-1,3-dioxolane
Carbonic acid, propylene ester
Carbonic acid, cyclic propylene ester
NSC 11784
Propylenester kyseliny uhlicite
Carbonic acid cyclic methylethylene ester
HSDB 6806
EINECS 203-572-1
Propylene carbonate [NF]
Carbonic acid, cyclic propylene ether
Propylenester kyseliny uhlicite [Czech]
BRN 0107913
AI3-19724
4-methyl-1,3-dioxolane-2-one
Propylene carbonate (NF)
Propylene carbonate, 99.5%
CAS-108-32-7
PC-HP
Propylene carbonate, 99.5%, anhydrous, AcroSeal(R)
Propylene carbonate [USAN]
Solvenon PC
propylen carbonate
MFCD00005385
Carbonic acid propylene

1, 3-Dioxolan-2-one, 4-methyl-
1,2-Propanediol cyclic carbonate
1,3-Dioxolan-2-one, 4-methyl- [ACD/Index Name]
107913
108-32-7 [RN]
4-Methyl-1,3-dioxol-2-one [ACD/IUPAC Name]
4-Methyl-1,3-dioxolan-2-on [German] [ACD/IUPAC Name]
4-Methyl-1,3-dioxolan-2-one [ACD/IUPAC Name]
4-Méthyl-1,3-dioxolan-2-one [French] [ACD/IUPAC Name]
4-Methyl-2-oxo-1,3-dioxolane
8D08K3S51E
Arconate 1000
Carbonic acid cyclic 1,2-propylene ester
Carbonic acid, cyclic propylene ether
Cyclic propylene carbonate
FF9650000
Jeffsol PC
MFCD00005385 [MDL number]
PC
PC-HP
Propylene carbonate [Wiki]
Propylene glycol cyclic carbonate
UNII:8D08K3S51E
(4S)-4-Methyl-1,3-dioxolan-2-one [ACD/IUPAC Name]
(R)-4-Methyl-1,3-dioxolan-2-one
(S)-4-Methyl-1,3-dioxolan-2-one
[108-32-7]
1,2-PDC
1,2-PROPANEDIOL CARBONATE
1,2-Propanediyl carbonate
1,2-PROPYLENE CARBONATE
1,2-Propylene glycol carbonate
1,2-Propylene-d6 Carbonate
1-Methylethylene carbonate
2-(Piperidin-4-yl)acetonitrile
202480-74-8 [RN]
2-Oxo-4-methyl-1,3-dioxolane
4-METHYL-1,3-DIOXOLANE-2-ONE
Arconate 5000
Arconate propylene carbonate
Carbonic acid cyclic methylethylene ester
Carbonic acid, cyclic propylene ester
Carbonic acid, propylene ester
CYCLIC 1,2-PROPYLENE CARBONATE
Cyclic methylethylene carbonate
Dipropylene carbonate
propylenecarbonate
Propylenester kyseliny uhlicite [Czech]
Propylenester kyseliny uhlicite
Solvenon PC
Texacar PC
WLN: T5OVOTJ D

OTHER LANGUAGES
(propán-1,2-diyl)-karbonát (sk)
4-metil-1,3-diossolan-2-one (it)
4-metylo-1,3-dioksolan-2-on (pl)
carbonate de propylène (fr)
carbonato de propileno (es)
carbonato de propileno (pt)
carbonato di propilene (it)
propilen carbonat (ro)
propilen karbonat (hr)
propilen karbonat (sl)
propilenkarbonatas (lt)
propilén-karbonát (hu)
propilēnkarbonāts (lv)
propyleencarbonaat (nl)
Propyleenikarbonaatti (fi)
propylencarbonat (da)
Propylencarbonat (de)
propylenkarbonat (no)
propylenkarbonat (sv)
propylenkarbonát (cs)
Propüleenkarbonaat (et)
węglan glikolu propylenowego (pl)
węglan propano-1,2-diylu (pl)
ανθρακικό προπυλένιο (el)
пропилен карбонат (bg)

CAS names
1,3-Dioxolan-2-one, 4-methyl-
Other
IUPAC names
1,2-Propanediol cyclic carbonate
1,2-Propylencarbonat
1,3-Dioxolan-2-one, 4-methyl-
1,3-dioxolan-2-one, 4-methyl-
2-(carboxyoxy)-1-methylethyl carbonate
4-methyl-1, 3-dioxolan-2-one
4-Methyl-1,3-Dioxolan-2-One
4-Methyl-1,3-dioxolan-2-one
4-methyl-1,3-dioxolan-2-one

propylen carbonate
Propylencarbonat
Propylencarbonate
PROPYLENE CARBONATE
Propylene Carbonate
Propylene carbonate
propylene carbonate
Propylene Carbonate
Propylene carbonate
propylene carbonate
Propylene carbonate 

Trade names
1,2-Propanediol carbonate
1,2-Propanediol cyclic carbonate
1,2-Propylene carbonate
1,3-Dioxolan-2-one, 4-methyl- (9CI)
1-Methylethylene carbonate
4-Methyl-1,3-dioxolan-2-one
4-Methyl-2-oxo-1,3-dioxolane
Cyclic 1,2-propylene carbonate
Cyclic methylethylene carbonate
Cyclic propylene carbonate
PC
Propylencarbonat
PROPYLENE CARBONATE
Propylene Carbonate
Propylene carbonate
Propylene glycol cyclic carbonate

Other identifiers: 104083-03-6
CAS number:104083-03-6
Deleted CAS number:108-32-7
CAS number: 127128-76-1
CAS number: 127128-76-1
Deleted CAS number:30141-77-6
CAS number:30141-77-6
Deleted CAS number:607-194-00-1

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