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D-Histidine hydrochloride monohydrate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

6341-24-8

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6341-24-8 Usage

Chemical Properties

White crystalline powder

Check Digit Verification of cas no

The CAS Registry Mumber 6341-24-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,4 and 1 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 6341-24:
(6*6)+(5*3)+(4*4)+(3*1)+(2*2)+(1*4)=78
78 % 10 = 8
So 6341-24-8 is a valid CAS Registry Number.
InChI:InChI=1/C6H9N3O2.ClH.H2O/c7-5(6(10)11)1-4-2-8-3-9-4;;/h2-3,5H,1,7H2,(H,8,9)(H,10,11);1H;1H2/t5-;;/m1../s1

6341-24-8 Well-known Company Product Price

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  • Sigma

  • (H7625)  D-Histidinemonohydrochloridemonohydrate  ≥98% (TLC)

  • 6341-24-8

  • H7625-5G

  • 2,026.44CNY

  • Detail

6341-24-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (R)-2-Amino-3-(1H-imidazol-4-yl)propanoic acid hydrochloride

1.2 Other means of identification

Product number -
Other names D-Histidine, hydrochloride

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:6341-24-8 SDS

6341-24-8Upstream product

6341-24-8Relevant academic research and scientific papers

Resolution of DL-racemic mixtures

-

Page column 7-8, (2008/06/13)

The present invention relates to a process for the resolution of DL-racemic mixtures of compounds which crystalize in the form of a conglumerate. Both, the D and L-enantiomers are obtained according to the invention in a industrially feasable process by adding chiral enantioselective polymers to the supersaturated solution of the racemat to inhibit crystalization of one enantiomer. Next a DL-racemic mixture of said compound is suspended in about twice the amount of the crystallized enantiomer. Consequently, the opposite enantiomer could be recovered by said suspension by physical separation.

DESIGN OF STEREOSPECIFIC INHIBITORS FOR CRYSTAL DISSOLUTION

Shimon, L. J. W.,Zbaida, D.,Addadi, L.,Leiserowitz, L.,Lahav, M.

, p. 199 - 222 (2007/10/02)

A new class of monomeric and polymeric crystal dissolution inhibitors has been prepared taking into consideration the packing arrangements and the morphologies of organic crystals.The efficiency of these inhibitors has been demonstrated by comparative morphological studies of α-glycine and by the kinetic resolution of the racemic conglomerates of his*HCl*H2O, threonine, glu*HCl, and 2,4-sec-phenetyl-3,5-dinitrobenzoate.

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