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N-(butan-2-yl)-2-hydroxypropanamide, also known as 2-hydroxypropionamide butyl ester, is a chemical compound with the molecular formula C7H15NO2. It is a colorless liquid with a molecular weight of 145.2 g/mol. N-(butan-2-yl)-2-hydroxypropanamide is formed by the esterification of 2-hydroxypropanamide (also known as glycolic acid amide) with butan-2-ol (also known as iso-butanol). It is used in various applications, including as a solvent, a chemical intermediate, and in the synthesis of other organic compounds. Due to its reactivity and potential applications, it is important to handle N-(butan-2-yl)-2-hydroxypropanamide with care, following proper safety protocols.

5422-35-5

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5422-35-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5422-35-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,2 and 2 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 5422-35:
(6*5)+(5*4)+(4*2)+(3*2)+(2*3)+(1*5)=75
75 % 10 = 5
So 5422-35-5 is a valid CAS Registry Number.

5422-35-5SDS

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 7,8-DIOXABICYCLO[3.2.1]OCT-6-YLMETHANAMINE

1.2 Other means of identification

Product number -
Other names N-sec-butyl-lactamide

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:5422-35-5 SDS

5422-35-5Downstream Products

5422-35-5Relevant academic research and scientific papers

FORUMLATIONS

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Page/Page column 4, (2009/09/25)

This invention relates to the use of lactamide compounds of formula (I): CH3CH(OH)C(=O)NR1R2, where R1 and R2 are each independently hydrogen; or C1-6 alkyl, C2-6 alkenyl or C3-6 cycloalkyl, each of which is optionally substituted by up to three substituents independently selected from phenyl, hydroxy, C1-5 alkoxy, morpholinyl and NR3R4 where R3 and R4 are each independently C1-3 alkyl; or phenyl optionally substituted by up to three substituents independently selected from C1-3 alkyl; or R1 and R2 together with the nitrogen atom to which they are attached form a morpholinyl, pyrrolidinyl, piperidinyl or azepanyl ring, each of which is optionally substituted by up to three substituents independently selected from C1-3 alkyl, in formulations to reduce the toxicity associated with other formulation components; to the use of certain lactamide compounds as solvents, especially in formulations, particularly in agrochemical formulations and in environmentally friendly formulations; to novel lactamide compounds; and to processes for preparing lactamide compounds.

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