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3715-92-2

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3715-92-2 Usage

Safety Profile

Poison by ingestion.Experimental teratogenic and reproductive effects.Questionable carcinogen with experimental neoplastigenicdata. Mutation data reported. Many N-nitroso compoundsare carcinogens. When heated to decomposition it emitsvery toxic fumes

Check Digit Verification of cas no

The CAS Registry Mumber 3715-92-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,7,1 and 5 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 3715-92:
(6*3)+(5*7)+(4*1)+(3*5)+(2*9)+(1*2)=92
92 % 10 = 2
So 3715-92-2 is a valid CAS Registry Number.
InChI:InChI=1/C3H5N3OS/c7-5-6-2-1-4-3(6)8/h1-2H2,(H,4,8)

3715-92-2SDS

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 1-nitrosoimidazolidine-2-thione

1.2 Other means of identification

Product number -
Other names NO-Etu

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:3715-92-2 SDS

3715-92-2Upstream product

3715-92-2Relevant articles and documents

The reaction of ethylenethiourea with nitrite and transnitrosation by N-nitrosoethylenethiourea

Yamamoto,Yamada,Tanimura

, p. 3678 - 3683 (1983)

Ethylenethiourea (ETU), a degradation and metabolic product of ethylenebisdithiocarbamate fungicides, was nitrosated by NaNO2 to form N-nitrosoethylenethiourea (NETU), ETU was nitrosated much more rapidly than morpholine and methylurea, which are easily nitrosatable compounds, and NETU formation increased with lowering of the pH. NETU was most unstable around pH 10 and was rather stable in strongly alkaline media above pH 12. The main decomposition reaction of NETU in acidic media was denitrosation. Transnitrosation by NETU to secondary amines gave high yields of nitrosamines at pH 3 and even at pH 5.

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