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Key Documents

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A1002

Sigma-Aldrich

Acetaldehyde oxime, mixture of syn and anti

99%

Sinónimos:

Acetaldoxime

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About This Item

Fórmula lineal:
CH3CH=NOH
Número de CAS:
107-29-9
Peso molecular:
59.07
Beilstein/REAXYS Number:
1209252
EC Number:
203-479-6
MDL number:
MFCD00002124
UNSPSC Code:
12352100
PubChem Substance ID:
24890491
NACRES:
NA.22

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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pictograms

FlameSkull and crossbones
GHS02,GHS06

signalword

Danger

Hazard Classifications

Acute Tox. 3 Inhalation - Acute Tox. 4 Oral - Aquatic Chronic 3 - Eye Irrit. 2 - Flam. Liq. 3

Storage Class

3 - Flammable liquids

wgk_germany

WGK 1

flash_point_f

104.0 °F - open cup

flash_point_c

40 °C - open cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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Sigma-Aldrich

438227

Hydroxylamine solution

Kazunobu Konishi et al.
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
Gabi Amitai et al.
Biomaterials, 31(15), 4417-4425 (2010-03-05)
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
M D Mikkelsen et al.
The Journal of biological chemistry, 275(43), 33712-33717 (2000-08-03)
Glucosinolates are natural plant products known as flavor compounds, cancer-preventing agents, and biopesticides. We report cloning and characterization of the cytochrome P450 CYP79B2 from Arabidopsis. Heterologous expression of CYP79B2 in Escherichia coli shows that CYP79B2 catalyzes the conversion of tryptophan
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