Welcome to LookChem.com Sign In|Join Free

CAS

  • or

84237-38-7

Post Buying Request

84237-38-7 Suppliers

Recommended suppliersmore

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

84237-38-7 Usage

Safety Profile

Confirmed carcinogen. When heated to decomposition it emits toxic vapors of NOx.

Check Digit Verification of cas no

The CAS Registry Mumber 84237-38-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,2,3 and 7 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 84237-38:
(7*8)+(6*4)+(5*2)+(4*3)+(3*7)+(2*3)+(1*8)=137
137 % 10 = 7
So 84237-38-7 is a valid CAS Registry Number.

84237-38-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name Pyridine, 3-(1-nitroso-2-pyrrolidinyl)-

1.2 Other means of identification

Product number -
Other names PYRIDINE,3-(1-NITROSO-2-PYRROLIDINYL)-

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:84237-38-7 SDS

84237-38-7Relevant articles and documents

N-nitrosation of myosmine yields HPB (4-hydroxy-1-(3-pyridyl)-1- butanone) and NNN (N-nitrosonornicotine)

Zwickenpflug, Wolfgang

, p. 392 - 394 (2007/10/03)

N-Nitrosonornicotine (NNN) is formed by synthetic or biological N- nitrosation of the tobacco alkaloid nornicotine. Following metabolic activation of NNN, DNA and protein adducts are formed releasing 4-hydroxy-1- (3-pyridyl)-1-butanone (HPB), an actual biomarker to differentiate between tobacco smokers and passive smokers, NNN and HPB can be prepared in a new one-step reaction by N-nitrosation of the nicotinoid myosmine which has been found not only in tobacco but also in nut products. The reaction was tested also in human gastric juice. The formation rate of NNN and HPB depends on the pH value in the reaction solutions. This is important under the aspect of myosmine uptake by humans from other biological sources and subsequent biological activation. The new reaction pathway indicates that human exposure to nicotinoid nitrosation products seems to be not restricted exclusively to tobacco.

Reaction of nicotine and sodium nitrite: Formation of nitrosamines and fragmentation of the pyrrolidine ring

Hecht,Chen,Ornaf,Jacobs,Adams,Hoffmann

, p. 72 - 76 (2007/10/04)

-

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 84237-38-7