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Isopropenyl acetate

CAS No.
108-22-5
Chemical Name:
Isopropenyl acetate
Synonyms
1-Acetoxy-1-methylethylene;2-Acetoxypropene;Isopropyl Acrtate;2-Acetoxypropylene;propen-2-ylacetate;IPA)Isopropenyl ace;Propen-2-yl acetate;ISOPROPENYL ACETATE;ISO-RPOPENYL ACETATE;1-propen-2-ylacetate
CBNumber:
CB9852741
Molecular Formula:
C5H8O2
Molecular Weight:
100.12
MDL Number:
MFCD00008709
MOL File:
108-22-5.mol
MSDS File:
SDS
Last updated:2023-09-12 19:13:56

Isopropenyl acetate Properties

Melting point -93 °C
Boiling point 94 °C (lit.)
Density 0.922 g/mL at 20 °C 0.909 g/mL at 25 °C (lit.)
vapor pressure 23 hPa (20 °C)
FEMA 4152 | ISOPROPENYL ACETATE
refractive index n20/D 1.401(lit.)
Flash point 66 °F
storage temp. Store below +30°C.
solubility 34g/l
form Liquid
color Clear colorless to very slightly yellow
PH 3 (34g/l, H2O, 20℃)
Odor at 100.00 %. ethereal acetic fruity sweet berry grape skin
Odor Type fruity
explosive limit 1.8%(V)
Water Solubility 34 g/L (20 ºC)
Merck 14,5203
JECFA Number 1835
BRN 1280347
LogP 1.28
Substances Added to Food (formerly EAFUS) ISOPROPENYL ACETATE
CAS DataBase Reference 108-22-5(CAS DataBase Reference)
FDA UNII 4AR9LAS337
NIST Chemistry Reference 1-Propen-2-ol, acetate(108-22-5)
EPA Substance Registry System Isopropenyl acetate (108-22-5)

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictogramsGHS hazard pictograms
GHS02,GHS07
Signal word  Danger
Hazard statements  H225-H335
Precautionary statements  P210
Hazard Codes  F
Risk Statements  11
Safety Statements  9-16-29-33
RIDADR  UN 2403 3/PG 2
WGK Germany  1
RTECS  UD4200000
10-21
Autoignition Temperature 439 °C DIN 51794
TSCA  Yes
HS Code  2915 39 00
HazardClass  3
PackingGroup  II
Toxicity LD50 orally in rats: 3.0 g/kg (Smyth)
NFPA 704
3
1 1

Isopropenyl acetate price More Price(17)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 10914 Isopropenyl acetate produced by Wacker Chemie AG, Burghausen, Germany, ≥99.0% (GC) 108-22-5 1kg $33.72 2024-03-01 Buy
Sigma-Aldrich 10914 Isopropenyl acetate produced by Wacker Chemie AG, Burghausen, Germany, ≥99.0% (GC) 108-22-5 25kg $1020 2024-03-01 Buy
Sigma-Aldrich 8.03138 Isopropenyl acetate for synthesis 108-22-5 100mL $35.4 2022-05-15 Buy
TCI Chemical A0035 Isopropenyl Acetate >98.0%(GC) 108-22-5 25mL $23 2024-03-01 Buy
TCI Chemical A0035 Isopropenyl Acetate >98.0%(GC) 108-22-5 500mL $53 2024-03-01 Buy
Product number Packaging Price Buy
10914 1kg $33.72 Buy
10914 25kg $1020 Buy
8.03138 100mL $35.4 Buy
A0035 25mL $23 Buy
A0035 500mL $53 Buy

Isopropenyl acetate Chemical Properties,Uses,Production

Description

Isopropenyl acetate is a kind of organic compound, corresponding to the acetate ester of the enol tautomer of acetone. It appears as a clear, colorless liquid with a fruit-like odor. It has a moderate solubility in water and a low flash point. It has a lower density than water but heavier vapor than the air. It is widely used as an industrial and consumer based solvent. For example, it is used as the principal precursor to acetylacetone and some other important chemicals. It can also be used as a kind of food additive. Moreover, it is also applied to coatings, cleaning fluids and printing inks as well as used as cosmetic and personal care solvent and fragrance solvents. It has various kinds of advantages including being a good resin solvent, belonging to a Non-HAP (hazardous air pollutant solvent), having mild odor and undergoing fast evaporating. It is manufactured through treatment of acetone with ketene. However, it is highly flammable and of certain toxicity, therefore proper protective measures should be used during the operation.

References

https://pubchem.ncbi.nlm.nih.gov/compound/Isopropenyl_acetate#section=Artificial-Sources
http://www.monumentchemical.com/documents/IPAc_TDS_MC.pdf
https://en.wikipedia.org/wiki/Isopropenyl_acetate

Chemical Properties

clear colorless to very slightly yellow liquid

Uses

Iodine in isopropenyl acetate is a unique catalyst for the acetylation of a variety of alcohols, phenols and amines under solvent free conditions. It is used as a solvent for cellulose, plastics, oil and fats. It is also a building block used for various organic synthesis.

Uses

Reagent for acylation of potential enols.

Definition

ChEBI: Isopropenyl acetate is an ester.

Synthesis Reference(s)

Journal of the American Chemical Society, 88, p. 2054, 1966 DOI: 10.1021/ja00961a043

General Description

A clear colorless liquid. Flash point near 60°F. Boiling point near 200°F. Less dense than water. Vapors heavier than air. Used to make other chemicals.

Air & Water Reactions

Highly flammable. Soluble in water.

Reactivity Profile

Isopropenyl acetate is an ester. Esters react with acids to liberate heat along with alcohols and acids. Strong oxidizing acids may cause a vigorous reaction that is sufficiently exothermic to ignite the reaction products. Heat is also generated by the interaction of esters with caustic solutions. Flammable hydrogen is generated by mixing esters with alkali metals and hydrides.

Hazard

Flammable, dangerous fire risk.

Health Hazard

May cause toxic effects if inhaled or absorbed through skin. Inhalation or contact with material may irritate or burn skin and eyes. Fire will produce irritating, corrosive and/or toxic gases. Vapors may cause dizziness or suffocation. Runoff from fire control or dilution water may cause pollution.

Fire Hazard

HIGHLY FLAMMABLE: Will be easily ignited by heat, sparks or flames. Vapors may form explosive mixtures with air. Vapors may travel to source of ignition and flash back. Most vapors are heavier than air. They will spread along ground and collect in low or confined areas (sewers, basements, tanks). Vapor explosion hazard indoors, outdoors or in sewers. May polymerize explosively when heated or involved in a fire. Runoff to sewer may create fire or explosion hazard. Containers may explode when heated. Many liquids are lighter than water.

Flammability and Explosibility

Flammable

Safety Profile

Moderately toxic by ingestion. A skin, eye, and mucous membrane irritant. A very dangerous fire hazard when exposed to heat or flame; can react vigorously with oxidizing materials. To fight fire, use alcohol foam, CO2, dry chemical. When heated to decomposition it emits acrid smoke and irritating fumes.

64-19-7
67-64-1
108-22-5
Synthesis of Isopropenyl acetate from Acetic acid and Acetone
Global( 298)Suppliers
Supplier Tel Email Country ProdList Advantage
Capot Chemical Co.,Ltd.
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View Lastest Price from Isopropenyl acetate manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Isopropenyl acetate pictures 2023-09-12 Isopropenyl acetate
108-22-5
US $0.00 / kg 1kg 99.00% 20tons Hebei Yanxi Chemical Co., Ltd.
Isopropenyl acetate pictures 2023-03-06 Isopropenyl acetate
108-22-5
US $10.50 / KG 1KG 99% 10 ton Hebei Guanlang Biotechnology Co,.LTD
Isopropenyl acetate pictures 2023-01-31 Isopropenyl acetate
108-22-5
US $0.00 / Kg/Drum 1Kg/Drum 99% 5000KG Hebei Mojin Biotechnology Co., Ltd
1-Propen-2-yl acetate ACETIC ACID ISOPROPENYL ESTER Acetatic acid,isopropenyl ester 1-METHYLVINYL ACETATE 1-PROPEN-2-OL ACETATE ISOPROPENYL ACETATE, WACKER QUALITY ISO-RPOPENYL ACETATE Essigsureisopropenylester ALPHA-Methylvinyl acetate 1-Methylvinyl acetate, IPA 1-Propene-2-ol=acetate Acetic acid 1-methylvinyl ester Acetic acid isopropenyl Isopropenyl acetate,99% Isopropenyl acetate,1-Methylvinyl acetate Isopropenyl acetate, 99% 250GR ISOPROPENYL ACETATE FOR SYNTHESIS Isopropenyl acetate (IPA) IPA)Isopropenyl ace Different allyl acetate Isopropenyl acetate 99% 1-propen-2-ylacetate 2-Acetoxypropene 2-Acetoxypropylene acetated’isopropenyle Acetic acid 1-methylethenyl ester Isopropenylester kyseliny octove isopropenylesterkyselinyoctove Propen-2-yl acetate propen-2-ylacetate propenylacetate(non-specificname) LABOTEST-BB LT00067724 ISOPROPENYL ACETATE ACETONE ENOL ACETATE Isopropyl Acrtate Isopropenyl Acetate > 1-Propen-2-ol, 2-acetate Isopropenyl acetate USP/EP/BP Isopropenyl Acetate extrapure, 99% 1-Acetoxy-1-methylethylene 108-22-5 108225 CH3CO2CCH3CH2 Building Blocks Carbonyl Compounds C2 to C5 Organic Building Blocks Esters Pharmaceutical intermediates