Welcome to LookChem.com Sign In|Join Free

CAS

  • or

13256-07-0

Post Buying Request

13256-07-0 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

13256-07-0 Usage

Chemical Properties

Yellow Viscous Liquid

Uses

A potent esophageal carcinogen

Safety Profile

Poison by ingestion, subcutaneous, and intraperitoneal routes. Suspected carcinogen with experimental carcinogenic, neoplas tigenic, and tumorigenic data. Mutation data reported. When heated to decomposition it emits toxic NO,. See also NITROSAMINES and N-NITROSO COMPOUNDS.

Check Digit Verification of cas no

The CAS Registry Mumber 13256-07-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,2,5 and 6 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 13256-07:
(7*1)+(6*3)+(5*2)+(4*5)+(3*6)+(2*0)+(1*7)=80
80 % 10 = 0
So 13256-07-0 is a valid CAS Registry Number.
InChI:InChI=1/C6H14N2O/c1-3-4-5-6-8(2)7-9/h3-6H2,1-2H3

13256-07-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name N-Amyl-N-methylnitrosamine

1.2 Other means of identification

Product number -
Other names N-methyl-N-pentylnitrous amide

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:13256-07-0 SDS

13256-07-0Relevant articles and documents

β-KETONITROSAMINES. SYNTHETIC EQUIVALENTS OF α-METHYLENE ALKYLAMINO ANIONS (-CH2NHR).

Saavedra, Joseph E.,Farnsworth, David W.,Farrelly, James G.

, p. 1147 - 1156 (2007/10/02)

β-Ketonitrosamines are important in the study of nitrosamine metabolism, carcinogenesis and in vivo alkylation.The enhanced acidity of protons at the α-carbon, as well as the ease of fragmentation of the title compounds establishes them as synthetic equivalents of α-methylene alkylamino anions (-CH2NHR).Anion formation is carried out with powdered sodium hydroxide - sodium carbonate in DMF or THF at 25 deg C.Reaction with an alkyl halide gives a good yield of the alkylated product.Retro-Claisen cleavage in aqueous basic media gives the corresponding dialkyl - nitrosamine or, with D2O, the deuterated analog.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 13256-07-0