(Z)-acetaldehyde oxime

Base Information Edit

Chemical Name:(Z)-acetaldehyde oxime
CAS No.:107-29-9
Molecular Formula:C2H5NO
Molecular Weight:59.0678
Hs Code.:2928.00
European Community (EC) Number:203-479-6
NSC Number:4974
UN Number:2332
UNII:IF220J2972
DSSTox Substance ID:DTXSID401016246
Nikkaji Number:J4.062B,J1.779.301B
Wikipedia:Acetaldoxime
Wikidata:Q2823824
Metabolomics Workbench ID:57526
Mol file:107-29-9.mol

Synonyms:(Z)-acetaldehyde oxime;(Z)-Acetaldoxime;cis-Acetaldehyde oxime;acetaldehyde, oxime, (1Z)-;(1Z)-acetaldehyde oxime;Acetaldehyde oxime, (1Z)-;Acetaldehyde, oxime, (Z)-;(1Z)-ethanal oxime;5775-72-4;UNII-IF220J2972;107-29-9;IF220J2972;Acetaldehyde, oxime;acetaldehydoxim-;UN 2332;acetaldehydeoxime;E-Acetaldoxime;(NZ)-N-ethylidenehydroxylamine;NA2332;WLN: QNU2;CHEBI:50719;NSC4974;DTXSID401016246;NSC-4974;F13401;A801662;Q2823824

Suppliers and Price of (Z)-acetaldehyde oxime

Supply Marketing:Edit

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

TRC
Acetaldoxime
25g
$ 50.00

TRC
Acetaldoxime
10g
$ 45.00

TCI Chemical
Acetaldoxime >99.0%(GC)
25mL
$ 30.00

Sigma-Aldrich
Acetaldehyde oxime, mixture of syn and anti 99%
25g
$ 44.90

Sigma-Aldrich
Acetaldoxime (mixture of cis and trans isomers) for synthesis. CAS 107-29-9, molar mass 59.07 g/mol., (mixture of cis and trans isomers) for synthesis
8410850250
$ 245.00

Sigma-Aldrich
Acetaldoxime (mixture of cis and trans isomers) for synthesis
250 mL
$ 234.95

Sigma-Aldrich
Acetaldoxime (mixture of cis and trans isomers) for synthesis. CAS 107-29-9, molar mass 59.07 g/mol., (mixture of cis and trans isomers) for synthesis
8410850050
$ 75.70

Sigma-Aldrich
Acetaldoxime (mixture of cis and trans isomers) for synthesis
50 mL
$ 72.52

Oakwood
Acetaldehydeoxime 98%
1g
$ 9.00

Frontier Specialty Chemicals
Acetaldehydeoxime,99%,mixtureofsynandanti
500g
$ 605.00

Total 67 raw suppliers

Chemical Property of (Z)-acetaldehyde oxime Edit

Chemical Property:

Appearance/Colour:white low melting solid or clear liquid
Vapor Pressure:13mmHg at 25°C
Melting Point:44-46 °C
Refractive Index:n20/D 1.426(lit.)
Boiling Point:114.5 °C at 760 mmHg
PKA:11.82±0.10(Predicted)
Flash Point:40 °C
PSA：32.59000
Density:0.969 g/cm³
LogP:0.46630
Storage Temp.:0-6°C
Solubility.:185g/l
Water Solubility.:soluble
XLogP3:-0.1
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:0
Exact Mass:59.037113783
Heavy Atom Count:4
Complexity:25.2
Transport DOT Label:Flammable Liquid

Purity/Quality:

99% ^*data from raw suppliers

Acetaldoxime ^*data from reagent suppliers

Safty Information:

Pictogram(s): Xi,Xn
Hazard Codes:Xi,Xn
Statements: 36/37/38-20/21/22-10-36-20/22
Safety Statements: 26-36-24/25-16

MSDS Files:: SDS file from LookChem

Useful:

Chemical Classes:Nitrogen Compounds -> Oximes
Canonical SMILES:CC=NO
Isomeric SMILES:C/C=N\O
Uses Pesticide intermediate, synthesis of pesticides “Methomyl”, “Thiodicarb”, etc.; organic synthesis intermediate. When melted, excellent solvent for many inorganic and organic compounds, organic synthesis, stabilizer, plasticizer, alcohol denaturant. Creation of acylamide through the aldehyde oxime one-pot method. With the presence of catalyst InCl3, acetaldehyde oxime replaces water and reacts with nitrile water to create acylamide at a high yield. Acetaldoxime is used as an oxygen scavenger in boiler water. It is also used as an intermediate in chemical synthesis and pharmaceuticals. It is involved in the rearrangement reaction to prepare acetamide by using nickel(II) acetate as a catalyst. It acts as a precursor to prepare heterocyclic compound such as spiroisoxazoline. Further, it is used to prepare alkylated(Z)-oximes by deprotonation followed by reaction with benzyl bromide.

Technology Process of (Z)-acetaldehyde oxime

There total 26 articles about (Z)-acetaldehyde oxime which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 97.0%