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2832-19-1

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2832-19-1 Usage

Description

N-Methylolchloroacetamide, also known as 2-Chloro-N-(hydroxymethyl)acetamide, is a N-hydroxymethyl derivative of chloroacetamide. It is a white or almost white crystalline powder that has been reported to be a formaldehyde releaser and an infrequent sensitizer to formaldehyde contact allergy. One of the methods reported for its synthesis is by the reaction of 2-chloracetamide with formaldehyde. It has high biocide action and is utilized as a preservative.

Uses

Used in Cooling Fluids and Cosmetics:
N-Methylolchloroacetamide is used as a preservative in cooling fluids and cosmetics due to its high biocide action, which helps maintain the freshness and longevity of these products.
Used in Organic Synthesis:
N-Methylolchloroacetamide is used as an organic building block, making it an important raw material and intermediate in the field of organic synthesis.
Used in Pharmaceuticals:
It is also utilized in the pharmaceuticals industry as a key intermediate for the synthesis of various drugs.
Used in Agrochemicals:
N-Methylolchloroacetamide is used as a vital intermediate in the production of agrochemicals, contributing to the development of effective agricultural products.
Used as a Dyestuff Intermediate:
It serves as an essential intermediate in the manufacturing of dyes, playing a crucial role in the dyeing and coloring processes.
Used in the Synthesis of 1-(aminomethyl)-2-methoxynaphthalene Hydrochloride:
N-Methylolchloroacetamide may be used as a reagent in the synthesis of 1-(aminomethyl)-2-methoxynaphthalene hydrochloride, a compound with potential applications in various industries.
Used as an Amidomethylating Reagent for N,N-dialkylanilines (Tscherniac-Einhorn Reaction):
It is employed as an amidomethylating reagent for N,N-dialkylanilines in the Tscherniac-Einhorn reaction, which is a significant process in the synthesis of various organic compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 2832-19-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,8,3 and 2 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 2832-19:
(6*2)+(5*8)+(4*3)+(3*2)+(2*1)+(1*9)=81
81 % 10 = 1
So 2832-19-1 is a valid CAS Registry Number.
InChI:InChI=1/C3H6ClNO2/c4-1-3(7)5-2-6/h6H,1-2H2,(H,5,7)

2832-19-1 Well-known Company Product Price

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  • CAS number
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  • Alfa Aesar

  • (A12247)  2-Chloro-N-(hydroxymethyl)acetamide, 98%   

  • 2832-19-1

  • 10g

  • 572.0CNY

  • Detail
  • Alfa Aesar

  • (A12247)  2-Chloro-N-(hydroxymethyl)acetamide, 98%   

  • 2832-19-1

  • 50g

  • 1375.0CNY

  • Detail

2832-19-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-chloro-N-(hydroxymethyl)acetamide

1.2 Other means of identification

Product number -
Other names N-hydroxymethylchloroacetic amide

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:2832-19-1 SDS

2832-19-1Relevant articles and documents

FUNGICIDAL PENFLUFEN MIXTURES

-

, (2014/04/03)

The invention relates to mixtures comprising penflufen, to the use of these mixtures for protecting industrial materials and to a method for treating industrial materials with the penflufen mixtures.

Bromonitrothienyldioxanes

-

, (2008/06/13)

The invention relates to novel 5-bromo-5-nitro-2-thienyl-1,3-dioxanes of the formula (I) in which R1, R2 and R3 are as defined in the description are highly suitable for use as biocides for protecting plants and industrial materials.

O-aryl dithiazole dioxides

-

, (2012/09/11)

The invention relates to new O-aryldithiazole dioxides, to two processes for their preparation, and to their use as pesticides in crop protection and in the protection of materials.

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