AZOXYMETHANE

Base Information

• Chemical Name: AZOXYMETHANE
• CAS No.: 25843-45-2
• Molecular Formula: C2H6 N2 O
• Molecular Weight: 74.0824
• Hs Code.: 2927000090
• Mol file: 25843-45-2.mol

Synonyms:Azoxymethane(7CI,8CI); NSC 171779

Chemical Property of AZOXYMETHANE

Chemical Property:

• Vapor Pressure: 59.7mmHg at 25°C
• Refractive Index: 1.4368 (estimate)
• Boiling Point: 92°Cat760mmHg
• Flash Point: 9.4°C
• PSA: 41.11000
• Density: 0.98g/cm³
• LogP: 0.73170
• Storage Temp.: −20°C

Purity/Quality:

98%,99%, ^*data from raw suppliers

Azoxymethane 13.4 M, ≥98% ^*data from reagent suppliers

Safty Information:

• Hazard Codes: T
• Statements: 45-46-10-25-34-36/38
• Safety Statements: 53-26-36/37/39-45

MSDS Files:

SDS file from LookChem

Useful:

• Uses: Azoxymethane (AOM), a gene mutation agent, may be used with dextran sulfate sodium (DSS) to create cancer models in laboratory animals which can be used to study mechanisms of cancer progression and chemoprevention.

Technology Process of AZOXYMETHANE

There total 7 articles about AZOXYMETHANE 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:

MeN((15)NO)OH → Azoxymethane (25843-45-2)

Guidance literature:

DOI:10.1039/b805329d

Reference yield:

(Z)-azomethane (4143-42-4,503-28-6) → azoxymethane (54168-20-6,87339-13-7,25843-45-2)

Guidance literature:

With Perbenzoic acid;

Reference yield:

→ azoxymethane (54168-20-6,87339-13-7,25843-45-2)

Guidance literature:

Azomethan markiert, m-Chlorperbenzoesaeure;

DOI:10.1002/jlcr.2590040210

upstream raw materials:

(Z)-azomethane

N-nitroso-O,N-dimethylhydroxylamine

methyllithium

6-hydroxyamino-1,3-dimethylpyrimidine-2,4(1H,3H)-dione

Refernces

• 1、 Zarovkina, N. Yu,Sazonova,Artemov,Fukin. "Chemistry of unsaturated arenetricarbonylchromium compounds 1. Reaction of (η6-arene)tricarbonylchromium complexes of nitrones with methyl phenylpropiolate". . p. 970 - 975. Retrieved 2015/02/05.
• 2、 Meesters, A. C. M.,Rueerger, H.,Rajeswari, K.,Benn, M. H.. "THE FORMATION OF AZOXYALKANES IN REACTIONS OF SOME ORGANOMETALLIC REAGENTS WITH N-nitroso-O,N-DIALKYLHYDROXYLAMINES: THE NONPHOTOCHEMICAL SYNTHESIS OF AN ACYCLIC (E)-AZOXYALKANE". . p. 264 - 268. Retrieved 2007/10/02.