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589918

Sigma-Aldrich

Methyl formate-12C

99.9 atom % 12C, 13C depleted

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About This Item

Linear Formula:
H12CO2CH3
CAS Number:
1196157-81-9
Molecular Weight:
60.04
MDL number:
MFCD00198117
UNSPSC Code:
12352202
PubChem Substance ID:
24881259

isotopic purity

99.9 atom % 12C

Quality Level

200

quality

13C depleted

bp

34 °C (lit.)

mp

-100 °C (lit.)

density

0.974 g/mL at 25 °C

mass shift

depleted

SMILES string

[H][12C](=O)OC

InChI

1S/C2H4O2/c1-4-2-3/h2H,1H3/i2+0

InChI key

TZIHFWKZFHZASV-ULIRUUBJSA-N

Related Categories

Packaging

This product may be available from bulk stock and can be packaged on demand. For information on pricing, availability and packaging, please contact Stable Isotopes Customer Service.

Pictograms

FlameExclamation mark
GHS02,GHS07

Signal Word

Danger

Precautionary Statements

P210 - P261 - P305 + P351 + P338

Hazard Classifications

Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Flam. Liq. 1 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

3 - Flammable liquids

WGK

WGK 2

Flash Point(F)

-16.6 °F - closed cup

Flash Point(C)

-27 °C - closed cup

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Daren J Burke et al.
The journal of physical chemistry. A, 119(26), 6837-6849 (2015-06-10)
We present the first detailed comparative study of the adsorption and thermal processing of the three astrophysically important C2O2H4 isomers glycolaldehyde, methyl formate, and acetic acid adsorbed on a graphitic grain analogue at 20 K. The ability of the individual
Daren J Burke et al.
The Journal of chemical physics, 143(16), 164704-164704 (2015-11-02)
The formation, chemical, and thermal processing of complex organic molecules (COMs) is currently a topic of much interest in interstellar chemistry. The isomers glycolaldehyde, methyl formate, and acetic acid are particularly important because of their role as pre-biotic species. It
Paula Urquhart et al.
Journal of lipid research, 56(8), 1419-1433 (2015-06-03)
Arachidonoyl ethanolamine (anandamide) and pros-taglandin ethanolamines (prostamides) are biologically active derivatives of arachidonic acid. Although available through different precursor phospholipids, there is considerable overlap between the biosynthetic pathways of arachidonic acid-derived eicosanoids and anandamide-derived prostamides. Prostamides exhibit physiological actions and
M Masoodi et al.
Leukemia, 28(7), 1381-1387 (2014-01-15)
Oleoylethanolamide (OEA) is a bioactive lipid that stimulates nuclear and G protein-coupled receptors and regulates appetite and fat metabolism. It has not previously been shown to have a role in cancer. However, a mass spectrometry-based lipidomics platform revealed the presence

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