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13325-11-6

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13325-11-6 Usage

Physical state

Colorless liquid

Odor

Faint amine odor

Primary use

Intermediate in the synthesis of pharmaceuticals and other organic compounds

Classification

Tertiary amine

Molecular structure

Six-carbon chain with a hydroxyl group and an amino group at the third carbon

Potential applications

Production of drugs, surfactants, and corrosion inhibitors

Handling precautions

Handle with caution and proper safety measures due to potential hazards if not used properly.

Check Digit Verification of cas no

The CAS Registry Mumber 13325-11-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,3,2 and 5 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 13325-11:
(7*1)+(6*3)+(5*3)+(4*2)+(3*5)+(2*1)+(1*1)=66
66 % 10 = 6
So 13325-11-6 is a valid CAS Registry Number.

13325-11-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-aminohexan-3-ol

1.2 Other means of identification

Product number -
Other names 2-amino-3-hexanol

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:13325-11-6 SDS

13325-11-6Downstream Products

13325-11-6Relevant articles and documents

Enzyme-Catalyzed Reactions, 8. - Stereoselective Synthesis of 2-Amino Alcohols from (R)- and (S)-Cyanohydrins

Effenberger, Franz,Gutterer, Beate,Ziegler, Thomas

, p. 269 - 273 (2007/10/02)

erythro-2-Amino alcohols (1R,2S)- and (1S,2R)-4 may be synthesized stereoselectively by addition of Grignard compounds to cyanohydrins (R)-, (S)-1 and their O-trimethylsilyl derivatives 3, respectively, followed by hydrogenation.The threo-2-amino alcohols (1S,2S)- and (1R,2R)-4 are easily accessible by inversion at C-1 of the (1R,2S) and (1S,2R) compounds.

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