Propyl acetate

Propyl acetate
Template:Longitem	Template:Unbulleted list
ChEBI	Template:Unbulleted list
ChemSpider	Template:Unbulleted list
DrugBank	Template:Unbulleted list
EC Number	Template:Unbulleted list
KEGG	Template:Unbulleted list
Template:Longitem	Template:Unbulleted list
RTECS number	Template:Unbulleted list
UN number	1276
	Script error: No such module "collapsible list".
	Script error: No such module "collapsible list".
Template:Longitem	Template:Chembox Elements/molecular formula
Molar mass	Template:Chem molar mass
Appearance	Colorless liquid
Odor	Mild, fruity
Density	0.89Script error: No such module "String".g/cm3
Melting point	Template:Chembox CalcTemperatures
Boiling point	Template:Chembox CalcTemperatures
Vapor pressure	25Script error: No such module "String".mmHg (20Script error: No such module "String".°C)
Template:Longitem	−65.91·10−6 cm3/mol
NFPA 704 (fire diamond)	Template:NFPA 704 diamond
Flash point	Template:Chembox CalcTemperatures
Template:Longitem	Template:Chembox CalcTemperatures
Explosive limits	1.7–8%
Template:Longitem	Ethyl acetate; Isopropyl acetate; n-butyl acetate; Isobutyl acetate
Template:Longitem	Propan-1-ol; Acetic acid

Template:Chembox image cell Template:Chembox image cell Template:Chembox AllOtherNames Template:Chembox headerbar Template:Chembox Indexlist Template:Chembox Jmol Template:Chembox ChEMBL Template:Chembox ECHA Template:Chembox E number Template:Chembox IUPHAR ligand Template:Chembox UNII Template:Chembox CompTox Template:Chembox headerbar Template:Chembox SolubilityInWater Template:Chembox headerbar Template:Chembox GHS (set)Template:Chembox Lethal amounts (set)Template:Chembox setHeader Template:Chembox setDatarow Template:Chembox setDatarow Template:Chembox setDatarow Template:Chembox headerbar Template:Chembox Datapage check Template:Chembox Footer

Template:Chembox Footer/trackingScript error: No such module "TemplatePar".Template:Short description

Propyl acetate, also known as propyl ethanoate, is an organic compound. Nearly 20,000 tons are produced annually for use as a solvent. This colorless liquid is known by its characteristic odor of pears. Due to this fact, it is commonly used in fragrances and as a flavor additive. It is formed by the esterification of acetic acid and propan-1-ol, often via Fischer–Speier esterification, with sulfuric acid as a catalyst and water produced as a byproduct.^[6]

References

↑ ^a ^b ^c ^d ^e ^f Script error: No such module "citation/CS1".
↑ ^a ^b Record in the GESTIS Substance Database of the Institute for Occupational Safety and HealthScript error: No such module "TemplatePar". Script error: No such module "TemplatePar".
↑ Template:IDLH
↑ Union Carbide Data Sheet. Vol. 1/25/1965
↑ Template:IDLH
↑ Script error: No such module "citation/CS1".

Script error: No such module "Check for unknown parameters".

External links

NIOSH Pocket Guide to Chemical Hazards
Acetic acid, propyl ester - Toxicity Data
N-Propyl Acetate MSDS

Template:Esters Template:Asbox

[PGCH-1] ↑ ^a ^b ^c ^d ^e ^f Script error: No such module "citation/CS1".

[GESTIS-2] Record in the GESTIS Substance Database of the Institute for Occupational Safety and HealthScript error: No such module "TemplatePar". Script error: No such module "TemplatePar".

[3] Template:IDLH

[4] Union Carbide Data Sheet. Vol. 1/25/1965

[5] Template:IDLH

[6] Script error: No such module "citation/CS1".

[1]

[2]

[6]

Propyl acetate

References

External links

Navigation menu

Search