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13552-21-1

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13552-21-1 Usage

Chemical Properties

colourless or slightly yellow liquid

General Description

Slightly yellow liquid.

Air & Water Reactions

Avoid exposing 1-AMINO-2-BUTANOL to air for prolonged periods of time . Water soluble.

Reactivity Profile

1-AMINO-2-BUTANOL is an aminoalcohol. Amines are chemical bases. They neutralize acids to form salts plus water. These acid-base reactions are exothermic. The amount of heat that is evolved per mole of amine in a neutralization is largely independent of the strength of the amine as a base. Amines may be incompatible with isocyanates, halogenated organics, peroxides, phenols (acidic), epoxides, anhydrides, and acid halides. Flammable gaseous hydrogen is generated by amines in combination with strong reducing agents, such as hydrides.

Fire Hazard

Flash point data are not available for 1-AMINO-2-BUTANOL, but 1-AMINO-2-BUTANOL is probably combustible.

Check Digit Verification of cas no

The CAS Registry Mumber 13552-21-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,5,5 and 2 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 13552-21:
(7*1)+(6*3)+(5*5)+(4*5)+(3*2)+(2*2)+(1*1)=81
81 % 10 = 1
So 13552-21-1 is a valid CAS Registry Number.

13552-21-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-Aminobutan-2-ol

1.2 Other means of identification

Product number -
Other names 2-Butanol, 1-amino-

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:13552-21-1 SDS

13552-21-1Relevant articles and documents

Formation of potentially prebiotic amphiphiles by reaction of β-hydroxy-n-alkylamines with cyclotriphosphate

Mullen, Lee B.,Sutherland, John D.

, p. 4166 - 4168 (2007)

(Chemical Equation Presented) The long and the short of it: In water, long-chain β-hydroxy-n-alkylamines are converted to their O-monophosphates by reaction with cyclotriphosphate. With short-chain pVhydroxy-n-alkylamines, N-triphosphates are formed instead. The difference results from the formation of surfactant assemblies from the long-chain compounds. This surfactant control of reactivity may be of relevance to the prebiotic formation of amphiphiles. P: phosphate unit.

HYDROXYPYRIDOXAZEPINES AS NRF2 ACTIVATORS

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Page/Page column 94, (2020/08/28)

The present invention relates hydroxypyridoxazepine compounds, methods of making them, pharmaceutical compositions containing them and their use as Nrf2 activators. In particular, the invention relates to compounds of Formula (I), and pharmaceutically acc

BISARYL AMIDES AS NRF2 REGULATORS

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Page/Page column 127, (2018/09/11)

The present invention relates to bisaryl amide analogs, pharmaceutical compositions containing them and their use as NRF2 activators. In particular, the invention relates to bisaryl heterocycles of Formula (I).

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