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N-NITROSO-N-METHYL-4-AMINOBUTYRIC ACID is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

61445-55-4

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61445-55-4 Usage

Chemical Properties

Yellow Oil

Check Digit Verification of cas no

The CAS Registry Mumber 61445-55-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,4,4 and 5 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 61445-55:
(7*6)+(6*1)+(5*4)+(4*4)+(3*5)+(2*5)+(1*5)=114
114 % 10 = 4
So 61445-55-4 is a valid CAS Registry Number.
InChI:InChI=1/C5H10N2O3/c1-7(6-10)4-2-3-5(8)9/h2-4H2,1H3,(H,8,9)

61445-55-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-[methyl(nitroso)amino]butanoic acid

1.2 Other means of identification

Product number -
Other names N-Methyl-N-(3-carboxypropyl)nitrosamine

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:61445-55-4 SDS

61445-55-4Relevant academic research and scientific papers

Structural effects on the n-nitrosation of amino acids

Gil, Rafael,Casado, Julio,Izquierdo, Carmen

, p. 495 - 504 (1997)

The relative importance of three different routes for the N-nitrosation of amino acids (nitrosation by N2O3, by NO+/NO2H2+ and by intramolecular migration of the nitroso group from the init

Synthesis method of N-nitroso-N-methyl-4-aminobutyric acid

-

Paragraph 0008; 0029; 0031-0032; 0034-0035; 0037, (2020/12/30)

The invention discloses a synthesis method of N-nitroso-N-methyl-4-aminobutyric acid, which comprises the following steps: carrying out alkali ring opening and hydrolysis on N-methyl pyrrolidone as shown in a formula I to form a compound as shown in a formula II, and reacting the compound as shown in the formula II with a nitrite to obtain a product as shown in a formula III. The method disclosedby the invention is simple in process route, simple and convenient to operate and mild in reaction condition, the target product N-nitroso-N-methyl-4-aminobutyric acid is obtained through two-step organic synthesis, and HNMR result shows that no impure peak exists.

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