Skip to Content
Merck
All Photos(3)

Key Documents

287725

Sigma-Aldrich

Butyl acetate

anhydrous, ≥99%

Synonym(s):

n-Butyl acetate

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
CH3COO(CH2)3CH3
CAS Number:
Molecular Weight:
116.16
Beilstein:
1741921
EC Number:
MDL number:
UNSPSC Code:
12352108
PubChem Substance ID:
NACRES:
NA.21

grade

anhydrous

Quality Level

vapor density

4 (vs air)

vapor pressure

15 mmHg ( 25 °C)
8 mmHg ( 20 °C)

Assay

≥99%

form

liquid

autoignition temp.

790 °F

expl. lim.

7.6 %

impurities

<0.005% water

evapn. residue

<0.0005%

refractive index

n20/D 1.394 (lit.)

pH

6.2 (20 °C, 5.3 g/L)

bp

124-126 °C (lit.)

mp

−78 °C (lit.)

density

0.88 g/mL at 25 °C (lit.)

SMILES string

CCCCOC(C)=O

InChI

1S/C6H12O2/c1-3-4-5-8-6(2)7/h3-5H2,1-2H3

InChI key

DKPFZGUDAPQIHT-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

General description

Butyl acetate is an aliphatic linear ester commonly used as an organic solvent in cosmetic and pharmaceutical industries and as a flavoring agent in food industry. It is a promising candidate as biofuel additive.

Pictograms

FlameExclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Flam. Liq. 3 - STOT SE 3

Target Organs

Central nervous system

Supplementary Hazards

Storage Class Code

3 - Flammable liquids

WGK

WGK 1

Flash Point(F)

80.6 °F - closed cup

Flash Point(C)

27 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Potential biofuel additive from renewable sources-kinetic study of formation of butyl acetate by heterogeneously catalyzed transesterification of ethyl acetate with butanol.
Ali SH, et al.
Bioresource Technology, 102(21), 10094-10103 (2011)
Yingying Jiang et al.
Advanced materials (Deerfield Beach, Fla.), 31(2), e1805761-e1805761 (2018-11-13)
Fast deposition of aligning ambipolar polymers for high-performance organic field-effect transistors (OFETs) and inverter circuits are highly desired for both scientific studies and industry applications. Here, large-area and ordered polymer films are prepared by a bar-coating method at a rate
Eagleson M.
Concise Encyclopedia Chemistry, 154-154 (1994)
Photocatalytic oxidation of butyl acetate in vapor phase on TiO2, Pt/TiO2 and WO3/TiO2 catalysts.
Keller V, et al.
J. Catal., 215(1), 129-138 (2003)
The spectrophotometric and fluorometric determination of aluminum with 8-hydroxyquinoline and butyl acetate extraction.
Bloom PR, et al.
Soil Science Society of America Journal. Soil Science Society of America, 42(5), 713-716 (1978)

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service