Skip to Content
Merck
All Photos(3)

Documents

306967

Sigma-Aldrich

Isopentyl acetate

anhydrous, ≥99%

Synonym(s):

Acetic acid 3-methylbutyl ester, Isoamyl acetate

Sign Into View Organizational & Contract Pricing
All Photos(3)

About This Item

Linear Formula:
CH3COOCH2CH2CH(CH3)2
CAS Number:
123-92-2
Molecular Weight:
130.18
Beilstein:
1744750
EC Number:
204-662-3
MDL number:
MFCD00008946
UNSPSC Code:
12352108
PubChem Substance ID:
57648464
NACRES:
NA.21

grade

anhydrous

Quality Level

100

vapor density

4.5 (vs air)

vapor pressure

5 mmHg ( 25 °C)

Assay

≥99%

form

liquid

autoignition temp.

680 °F

expl. lim.

7.5 %

impurities

<0.005% water

evapn. residue

<0.0005%

refractive index

n20/D 1.4 (lit.)

bp

142 °C/756 mmHg (lit.)

mp

−78 °C (lit.)

density

0.876 g/mL at 25 °C (lit.)

SMILES string

CC(C)CCOC(C)=O

InChI

1S/C7H14O2/c1-6(2)4-5-9-7(3)8/h6H,4-5H2,1-3H3

InChI key

MLFHJEHSLIIPHL-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Application

Isopentyl acetate can be used as a green solvent for the extraction of target compounds from complex matrices.

Pictograms

Flame
GHS02

Signal Word

Warning

Hazard Statements

H226

Hazard Classifications

Flam. Liq. 3

Supplementary Hazards

EUH066

Storage Class Code

3 - Flammable liquids

WGK

WGK 1

Flash Point(F)

91.4 °F - closed cup

Flash Point(C)

33 °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
STBK4821
SHBM5515
SHBJ0997
SHBG4648V
SHBF2582V

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.

Search for a COA

Already Own This Product?

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

Visit the Document Library

Biomonitoring of pesticides in urine by using isoamyl acetate as a sustainable extraction solvent
Journal of Pharmaceutical and Biomedical Analysis, 223, 115150-115150 (2023)
Miao Jing et al.
Nature methods, 17(11), 1139-1146 (2020-09-30)
The ability to directly measure acetylcholine (ACh) release is an essential step toward understanding its physiological function. Here we optimized the GRABACh (GPCR-activation-based ACh) sensor to achieve substantially improved sensitivity in ACh detection, as well as reduced downstream coupling to
David Tadres et al.
PLoS biology, 18(7), e3000712-e3000712 (2020-07-15)
Tools enabling closed-loop experiments are crucial to delineate causal relationships between the activity of genetically labeled neurons and specific behaviors. We developed the Raspberry Pi Virtual Reality (PiVR) system to conduct closed-loop optogenetic stimulation of neural functions in unrestrained animals.
Atsushi Ugajin et al.
PloS one, 7(3), e32902-e32902 (2012-03-21)
Anti-predator behaviors are essential to survival for most animals. The neural bases of such behaviors, however, remain largely unknown. Although honeybees commonly use their stingers to counterattack predators, the Japanese honeybee (Apis cerana japonica) uses a different strategy to fight
Hiroshi Sahara et al.
Journal of bioscience and bioengineering, 108(5), 359-364 (2009-10-07)
By application of the high-efficiency loss of heterozygosity (HELOH) method for disrupting genes in diploid sake yeast (Kotaka et al., Appl. Microbiol. Biotechnol., 82, 387-395 (2009)), we constructed, from a heterozygous integrant, a homozygous diploid that overexpresses the alcohol acetyltransferase
View All Related Papers

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