A1002
Acetaldehyde oxime, mixture of syn and anti
99%
Synonym(s):
Acetaldoxime
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About This Item
Linear Formula:
CH3CH=NOH
CAS Number:
Molecular Weight:
59.07
Beilstein:
1209252
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
Assay
99%
form
liquid
refractive index
n20/D 1.426 (lit.)
bp
115 °C (lit.)
density
0.969 g/mL at 25 °C (lit.)
storage temp.
2-8°C
SMILES string
C\C=N\O
InChI
1S/C2H5NO/c1-2-3-4/h2,4H,1H3/b3-2+
InChI key
FZENGILVLUJGJX-NSCUHMNNSA-N
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Related Categories
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 3 Inhalation - Acute Tox. 4 Oral - Aquatic Chronic 3 - Eye Irrit. 2 - Flam. Liq. 3
Storage Class Code
3 - Flammable liquids
WGK
WGK 1
Flash Point(F)
104.0 °F - open cup
Flash Point(C)
40 °C - open cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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The Journal of biological chemistry, 279(46), 47619-47625 (2004-09-02)
Aldoxime dehydratase (OxdA), which is a novel heme protein, catalyzes the dehydration of an aldoxime to a nitrile even in the presence of water in the reaction mixture. The combination of site-directed mutagenesis of OxdA (mutation of all conserved histidines
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We report the synthesis of new polymers based on a dimethylacrylamide-methacrylate (DMAA-MA) co-polymer backbone that support both chemical and biological agent decontamination. Polyurethanes containing the redox enzymes glucose oxidase and horseradish peroxidase can convert halide ions into active halogens and
Weng-Keong Loke et al.
European journal of pharmacology, 442(3), 279-287 (2002-06-18)
O-Substituted aldoximes of the cholinesterase reactivator pralidoxime (O-methyl 1, O-benzyl 2, O-propynyl 3 and O-butynyl 4 derivatives) were synthesized and found to exhibit strong binding affinities for muscarinic receptors in rat brain, heart and submandibulary glands. The aldoximes were noncompetitive
K Mlícková et al.
Biochimie, 83(11-12), 995-1002 (2002-03-07)
The reactions of pea diamine oxidase (PSAO) and 2-phenylethylamine oxidase from Arthrobacter globiformis (AGAO) with pyridine-derived oximes were studied. Pyridine carbaldoximes and alkyl pyridyl ketoximes act as strong non-competitive inhibitors of the enzymes. The inhibition constants K(i) of these compounds
Yasuhisa Asano
Journal of biotechnology, 94(1), 65-72 (2002-01-17)
As a typical example of screening for a microbial biocatalyst from nature, isolation of aldoxime-degrading microorganisms, characterization of a new enzyme phenylacetaldoxime dehydratase, and application of this enzyme to nitrile synthesis are described. The pathway in which aldoximes are successively
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