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45999

Sigma-Aldrich

Methyl acetate

suitable for HPLC, ≥99.8%

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About This Item

Linear Formula:
CH3COOCH3
CAS Number:
79-20-9
Molecular Weight:
74.08
Beilstein:
1736662
EC Number:
201-185-2
MDL number:
MFCD00008711
UNSPSC Code:
12190000
PubChem Substance ID:
329757046
NACRES:
NA.01

vapor density

2.55 (vs air)

vapor pressure

165 mmHg ( 20 °C)

Assay

≥99.8% (GC)
≥99.8%

form

liquid

autoignition temp.

936 °F

shelf life

limited shelf life, expiry date on the label

expl. lim.

16 %

technique(s)

HPLC: suitable

impurities

≤0.05% water

evapn. residue

≤0.001%

refractive index

n20/D 1.361 (lit.)
n20/D 1.362

bp

57-58 °C (lit.)

mp

−98 °C (lit.)

density

0.934 g/mL at 25 °C

solvent strength ε (Al2O3)

0.60

λ

1 cm path, H2O reference

UV absorption

λ: 255 nm Amax: 1.0
λ: 275 nm Amax: 0.1
λ: 300 nm Amax: 0.01

SMILES string

COC(C)=O

InChI

1S/C3H6O2/c1-3(4)5-2/h1-2H3

InChI key

KXKVLQRXCPHEJC-UHFFFAOYSA-N

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Application

  • Agglomeration of celecoxib by quasi-emulsion solvent diffusion method without stabilizer: effect of good solvent.: This research explored the agglomeration of celecoxib using the quasi-emulsion solvent diffusion method, highlighting the role of methyl acetate as a good solvent to improve particle size and distribution without the need for stabilizers (Maghsoodi & Nokhodchi, 2018).
  • Formulation and in vitro evaluation of ketoprofen in palm oil esters nanoemulsion for topical delivery.: The formulation and evaluation of ketoprofen in a nanoemulsion system for topical delivery were examined, with methyl acetate used as a solvent to enhance solubility and stability of the active ingredient (Sakeena et al., 2010).
  • Preparation of surfactant-free nanoparticles of methacrylic acid copolymers used for film coating.: This paper presented a method for preparing surfactant-free nanoparticles using methyl acetate as a solvent, emphasizing its role in the formation of uniform nanoparticle dispersions for coating applications (Nguyen et al., 2006).

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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

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Jeanne Mager Stellman
Encyclopaedia of Occupational Health and Safety: Guides, indexes, directory, 104-156 (1998)
Sergii Yakunin et al.
Nature communications, 12(1), 981-981 (2021-02-14)
Traditional fluorescence-based tags, used for anticounterfeiting, rely on primitive pattern matching and visual identification; additional covert security features such as fluorescent lifetime or pattern masking are advantageous if fraud is to be deterred. Herein, we present an electrohydrodynamically printed unicolour
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
Nicolas Salem et al.
Molecular imaging and biology : MIB : the official publication of the Academy of Molecular Imaging, 13(1), 140-151 (2010-04-20)
Studies have established the value of [(methyl)1-(11)C]-acetate ([(11)C]Act) combined with 2-deoxy-2[(18)F]fluoro-D-glucose (FDG) for detecting hepatocellular carcinoma (HCC) using positron emission tomography (PET). In this study, the metabolic fate of [(11)C]Act in HCC was characterized. Experiments with acetic acid [1-(14)C] sodium
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
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