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589918

Sigma-Aldrich

Methyl formate-12C

99.9 atom % 12C, 13C depleted

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About This Item

Formula condensata:
H12CO2CH3
Numero CAS:
1196157-81-9
Peso molecolare:
60.04
Numero MDL:
MFCD00198117
Codice UNSPSC:
12352202
ID PubChem:
24881259

Purezza isotopica

99.9 atom % 12C

Qualità

13C depleted

P. ebollizione

34 °C (lit.)

Punto di fusione

-100 °C (lit.)

Densità

0.974 g/mL at 25 °C

Spostamento di massa

depleted

Stringa SMILE

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

InChI

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

Categorie correlate

Confezionamento

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.

Pittogrammi

FlameExclamation mark
GHS02,GHS07

Avvertenze

Danger

Indicazioni di pericolo

H224,H302 + H332,H319,H335

Classi di pericolo

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

Organi bersaglio

Respiratory system

Codice della classe di stoccaggio

3 - Flammable liquids

Classe di pericolosità dell'acqua (WGK)

WGK 2

Punto d’infiammabilità (°F)

-16.6 °F - closed cup

Punto d’infiammabilità (°C)

-27 °C - closed cup

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Certificati d'analisi (COA)

Lot/Batch Number

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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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