Acetic anhydride

Code: 91204-25ML-F D2-231

Application

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Suitable for the derivatization of acetyl, acetaminophen, alcohols, aldoses and partially methylated...


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€88.00 EACH
€108.24 inc. VAT

Application

Learn more in the Product Information

Suitable for the derivatization of acetyl, acetaminophen, alcohols, aldoses and partially methylated aldoses, aldosterone, amines, amino acids, amino sugars (in polysaccharides), amino sugar methyl glycosides, 2-amino-2-deoxyhexoses, arginyl peptides, aryl sulfate esters, bile acids, carbamates, carbohydrates, cerebrosides, cystine and cysteine (in peptides), desmethyldoxepin, 3,4-dihydroxyphenylglycol, estrogens, glycitols, hexopyranosides, hexosamines, hydroxamic acids, hydroxyamines, n-hydroxycarbamates, hydroxy steroids, inositols, 4-methoxy and 3,4-dimethoxyphenethylamine, methyl ester, methyl(methyl O-methyl-a-D-glucopyranosid)uronates, nucleosides, nucleoside bases and sugars, partially methylated pentose and hexŒs, peptides, phenolalkylamines, phenylethylamines, polysaccharide constituents, postaglandins A,B and E, serotonin, sialic acids, sugars, natural sugars and tryptamine.

General description

Acylation, an alternative to silylation, enables the conversion of compounds that comprise of active hydrogens (-OH, -SH and -NH) into esters, thiŒsters, and amides by the action of a carboxylic acid or derivative. The carbonyl group adjacent to the halogenated carbons favors the improvement of electron capture detector (ECD) response. Acylation has several benefits: It increases the stability of compounds by protecting unstable groups. It may render volatility on substances like carbohydrates or amino acids, that have several polar groups that they are non-volatile and generally decompose on heating. It allows the separations not possible with underivatized compounds. Compounds are detectable at very low levels with an ECD.Acetic anhydride is a reagent utilized to form fragmentation-directing derivatives for GC/MS analysis.

Acetic anhydride is an esterification agent which is corrosive to metals. It is a colourless liquid with strong vinegar-like odour. It is mostly used in making plastics, fibers, pharmaceuticals, dyes and explosives.

Legal Information

LiChropur is a trademark of Merck KGaA, Darmstadt, Germany

Other Notes

Reagent for acetic anhydride, acetyl, n-acetyl, n-acetyl-n, o-acetyl, acetate, aldononitrile acetate, aminoglycitol acetate, aryl acetate, permethyl acetyl, methyl ester, trifluoroacetyl, bis-trimethylsilyl, trimethylsilyl polyamino alcohol, and O-trimethylsilyl (TMS).

Packaging

10×1 mL in glass insert

assay≥99.0%, ≥99.0% (GC)
autoignition temp.629 °F
bp138-140 °C (lit.)
density1.08 g/mL (lit.)
evapn. residue≤0.003%
expl. lim.10.3 %
formliquid
gradefor GC derivatization
InChI keyWFDIJRYMOXRFFG-UHFFFAOYSA-N
InChI1S/C4H6O3/c1-3(5)7-4(2)6/h1-2H3
mp−73 °C (lit.)
Quality Level100
qualityLiChropur
reaction suitabilityreagent type: derivatization reagentreaction type: Acylations
refractive indexn20/D 1.390 (lit.)
SMILES stringCC(=O)OC(C)=O
solubilityH2O: slightly soluble
technique(s)gas chromatography (GC): suitable
vapor density3.5 (vs air)
vapor pressure10 mmHg ( 36 °C), 4 mmHg ( 20 °C)
Cas Number108-24-7
Hazard Class8
Un Number1715
Pack GroupII
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