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1-nitrosopyrrolidin-2-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

65734-39-6

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65734-39-6 Usage

Chemical classification

1-Nitrosopyrrolidin-2-ol is a nitrosamine.

Physical state

It is a pale yellow solid at room temperature.

Uses

It is used mainly as an intermediate in the synthesis of other organic compounds, such as pharmaceuticals and agricultural chemicals.

Industrial byproduct

It is found as a byproduct of certain industrial processes, including the synthesis of rubber accelerators and antioxidants.

Potential health risk

NOP-OH is considered to be potentially carcinogenic, as nitrosamines are known to be cancer-causing agents.

Check Digit Verification of cas no

The CAS Registry Mumber 65734-39-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,7,3 and 4 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 65734-39:
(7*6)+(6*5)+(5*7)+(4*3)+(3*4)+(2*3)+(1*9)=146
146 % 10 = 6
So 65734-39-6 is a valid CAS Registry Number.

65734-39-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-nitrosopyrrolidin-2-ol

1.2 Other means of identification

Product number -
Other names 2-Pyrrolidinol,1-nitroso

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:65734-39-6 SDS

65734-39-6Downstream Products

65734-39-6Relevant academic research and scientific papers

Cyclic α-acetoxynitrosamines: Mechanisms of decomposition and stability of α-hydroxynitrosamine and nitrosiminium ion reactive intermediates

Chahoua, Latifa,Cai, Hongliang,Fishbein, James C.

, p. 5161 - 5169 (2007/10/03)

A study of the kinetics and mechanism of the decay of α-acetoxy-N- nitrosopyrrolidine and α-acetoxy-N-nitrosopiperidine are reported. The compounds differ in reactivity by more than 2 orders of magnitude at physiological pH. On the basis of thermodynamic

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