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615-53-2

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615-53-2 Usage

Chemical Properties

Yellow Oil

Uses

N-Methyl-N-nitrosourethane is a nitrosamide which causes chromosomal damage in HeLa cells. It is also used in the synthesis of antifungal agents such as azoxybacillin.

General Description

Solid.

Reactivity Profile

N-NITROSO-N-METHYLURETHANE is a N-nitrosated carbamate ester. Incompatible with strong acids and bases. Especially incompatible with strong reducing agents such as hydrides. Flammable gaseous hydrogen may be produced by the combination with active metals or nitrides Incompatible with oxidizing acids, peroxides, and hydroperoxides.

Health Hazard

TOXIC; inhalation, ingestion or skin contact with material may cause severe injury or death. Contact with molten substance may cause severe burns to skin and eyes. Avoid any skin contact. Effects of contact or inhalation may be delayed. Fire may produce irritating, corrosive and/or toxic gases. Runoff from fire control or dilution water may be corrosive and/or toxic and cause pollution.

Fire Hazard

Non-combustible, substance itself does not burn but may decompose upon heating to produce corrosive and/or toxic fumes. Some are oxidizers and may ignite combustibles (wood, paper, oil, clothing, etc.). Contact with metals may evolve flammable hydrogen gas. Containers may explode when heated.

Safety Profile

Confirmed carcinogen with experimental carcinogenic, tumorigenic, and teratogenic data. Poison by ingestion, intraperitoneal, subcutaneous, and intravenous routes. Moderately toxic by inhalation. Experimental reproductive effects. Mutation data reported. Has been implicated as a transplacental brain carcinogen. Combustible when exposed to heat, sparks, open flame, and powerful oxidizers. Explodes when heated. A storage hazard. When heated to decomposition it emits toxic fumes of NOx.

Check Digit Verification of cas no

The CAS Registry Mumber 615-53-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,1 and 5 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 615-53:
(5*6)+(4*1)+(3*5)+(2*5)+(1*3)=62
62 % 10 = 2
So 615-53-2 is a valid CAS Registry Number.
InChI:InChI=1/C4H8N2O3/c1-3-9-4(7)6(2)5-8/h3H2,1-2H3

615-53-2 Well-known Company Product Price

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  • (Code)Product description
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  • TCI America

  • (N0265)  N-Methyl-N-nitrosourethane  >95.0%(GC)

  • 615-53-2

  • 5g

  • 290.00CNY

  • Detail
  • TCI America

  • (N0265)  N-Methyl-N-nitrosourethane  >95.0%(GC)

  • 615-53-2

  • 25g

  • 980.00CNY

  • Detail

615-53-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl N-methyl-N-nitrosocarbamate

1.2 Other means of identification

Product number -
Other names N-Nitroso-N-methyl-urethan

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:615-53-2 SDS

615-53-2Relevant articles and documents

IMPROVEMENTS IN OR RELATING TO ORGANIC COMPOUNDS

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Page/Page column 18-19, (2015/05/06)

A process of converting a carbon-carbon multiple bond to a cyclopropane ring, comprising the addition of a N-alkyl-N-nitroso compound to a mixture of alkene precursor, aqueous base and Pd(II)-catalyst, with the N-alkyl-N-nitroso compound obtained directly from an alkyl amine derivative, NaNO2 and an acid via phase separation of the N-alkyl-N-nitroso compound from the aqueous phase.

Formation of Nitrosamines by Alkylation of Diazotates

Cooper, Curt S.,Peyton, Albert L.,Weinkam, Robert J.

, p. 4116 - 4119 (2007/10/02)

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