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W267619

Sigma-Aldrich

Methyl acetate

natural, 98%, FG

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About This Item

Linear Formula:
CH3COOCH3
CAS Number:
79-20-9
Molecular Weight:
74.08
FEMA Number:
2676
Beilstein:
1736662
EC Number:
201-185-2
Council of Europe no.:
213c
MDL number:
MFCD00008711
UNSPSC Code:
12164502
PubChem Substance ID:
24901242
Flavis number:
9.023
NACRES:
NA.21
grade:
FG
Halal
Kosher
natural
food allergen:
no known allergens
Pricing and availability is not currently available.

grade

FG
Halal
Kosher
natural

Quality Level

400

reg. compliance

EU Regulation 1334/2008 & 178/2002
FDA 21 CFR 117
FDA 21 CFR 175.105

vapor density

2.55 (vs air)

vapor pressure

165 mmHg ( 20 °C)

Assay

98%

form

liquid

autoignition temp.

936 °F

expl. lim.

16 %

refractive index

n20/D 1.361 (lit.)

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1 of 4

This Item
W2676005.8959345997
Methyl acetate natural, 98%, FG

W267619

Methyl acetate

Methyl acetate ≥98%, FG

W267600

Methyl acetate

Methyl acetate 99.5%, anhydrous

5.89593

Methyl acetate

Methyl acetate analytical standard

45997

Methyl acetate

organoleptic

ethereal; fruity; sweet

organoleptic

fruity; ethereal; sweet

organoleptic

-

organoleptic

-

food allergen

no known allergens

food allergen

no known allergens

food allergen

-

food allergen

-

documentation

see Safety & Documentation for available documents

documentation

see Safety & Documentation for available documents

documentation

-

documentation

-

assay

98%

assay

≥98%

assay

99.5%

assay

≥99.9% (GC)

density

0.934 g/mL at 25 °C

density

0.934 g/mL at 25 °C

density

0.934 g/mL at 25 °C

density

0.934 g/mL at 25 °C

Pictograms

FlameExclamation mark
GHS02,GHS07

Signal Word

Danger

Hazard Statements

H225,H319,H336

Hazard Classifications

Eye Irrit. 2 - Flam. Liq. 2 - STOT SE 3

Target Organs

Central nervous system

Supplementary Hazards

EUH066

Storage Class Code

3 - Flammable liquids

WGK

WGK 1

Flash Point(F)

8.6 °F - closed cup

Flash Point(C)

-13 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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    Certificates of Analysis (COA)

    Lot/Batch Number
    SHBN7782
    SHBL6420
    MKCG6517
    MKCF3825
    STBG8562

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    DeLu Tyler Yin et al.
    Chemistry (Weinheim an der Bergstrasse, Germany), 18(26), 8130-8139 (2012-05-24)
    Several serine hydrolases catalyze a promiscuous reaction: perhydrolysis of carboxylic acids to form peroxycarboxylic acids. The working hypothesis is that perhydrolases are more selective than esterases for hydrogen peroxide over water. In this study, we tested this hypothesis, and focused
    M L Senent et al.
    The Journal of chemical physics, 138(4), 044319-044319 (2013-02-08)
    Highly correlated ab initio calculations (CCSD(T)) are used to compute gas phase spectroscopic parameters of three isotopologues of the methyl acetate (CH(3)COOCH(3), CD(3)COOCH(3), and CH(3)COOCD(3)), searching to help experimental assignments and astrophysical detections. The molecule shows two conformers cis and
    Marco Candelaresi et al.
    The journal of physical chemistry. A, 113(46), 12783-12790 (2009-10-02)
    The solvation dynamics of methyl acetate in heavy water are analyzed by means of two-dimensional infrared spectroscopy, in conjunction with Car-Parrinello molecular dynamics simulations. The C horizontal lineO stretching infrared band of methyl acetate in water splits into a doublet
    Franc Avbelj et al.
    Proceedings of the National Academy of Sciences of the United States of America, 106(9), 3137-3141 (2009-02-10)
    Recent calorimetric measurements of the solvation enthalpies of some dipeptide analogs confirm our earlier prediction that the principle of group additivity is not valid for the interaction of the peptide group with water. We examine the consequences for understanding the
    Benjamin Bechem et al.
    The Journal of organic chemistry, 75(5), 1795-1798 (2010-02-06)
    5-Substituted-2-furan methanols 1a-c are subject to enantioselective carbonyl allylation, crotylation and tert-prenylation upon exposure to allyl acetate, alpha-methyl allyl acetate, or 1,1-dimethylallene in the presence of an ortho-cyclometalated iridium catalyst modified by (R)-Cl,MeO-BIPHEP, (R)-C3-TUNEPHOS, and (R)-C3-SEGPHOS, respectively. In the presence
    View All Related Papers

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