6341-24-8

Basic information

• Product Name: D-Histidine hydrochloride monohydrate
• Synonyms: D-HISTIDINE HCL;d-histidine,monohydrochloride;D-α-Amino-β-(4-imidazolyl)propionic acid monohydrochloride;d-histidineHClmonohydrate;D-Histidine monohydrate monohydrochloride;D-2-Amino-3-(4-imidazolyl)propionic acid hydrochloride monohydrate;D-HISTIDINE HYDROCHLORIDE MONOHYDRATE 99%;D-Histidine hydrochloride monohydrate,99%
• CAS NO: 6341-24-8
• Molecular Formula: C₆H₁₀N₃O₂*Cl
• Molecular Weight: 209.63
• EINECS: 228-733-3
• Mol File: 6341-24-8.mol
• Article Data: 3

Chemical Properties

• Melting Point: 254 °C (dec.)(lit.)
• Appearance: White/Powder
• Storage Temp.: Store at RT.
• Water Solubility: Soluble
• BRN: 4161356
• CAS DataBase Reference: D-Histidine hydrochloride monohydrate(CAS DataBase Reference)
• NIST Chemistry Reference: D-Histidine hydrochloride monohydrate(6341-24-8)
• EPA Substance Registry System: D-Histidine hydrochloride monohydrate(6341-24-8)

Safety Data

• Safety Statements: 22-24/25
• WGK Germany: 3
• Hazardous Substances Data: 6341-24-8(Hazardous Substances Data)

Usage

Chemical Properties

White crystalline powder

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

Upstream product

• 6459-59-2 histidine hydrochloride 

Downstream Products

• 117365-14-7 (5R)-5-(4-imidazolylmethyl)-3-<(R)-1-phenylethyl>-2,4-imidazolidinedione 
• 134540-80-0 (5R)-5-(4-imidazolylmethyl)-3-(4-methylphenyl)-2,4-imidazolidinedione 
• 4467-54-3 (R)-histidine methyl ester dihydrochloride 
• 1399858-69-5 Z-L-Lys-Z-D-His-OMe 
• 1399858-66-2 Z-L-Val-D-His-OMe 
• 1399858-68-4 Z-L-Tyr(Bn)-D-His-OMe 
• 1399858-74-2 Z-L-Trp-D-His-OMe 
• 1399858-75-3 Z-L-Ser(tBu)-D-His-OMe 
• 1399858-76-4 Z-L-Met-D-His-OMe 
• 1399858-65-1 Z-L-His-D-His-OMe 
• 1399858-67-3 Z-L-Glu(γBn)-D-His-OMe 
• 1399858-71-9 Z-L-Asn-D-His-OMe 
• 75614-85-6 R-(-)-4-(2-Amino-3-chlorpropyl)-imidazol-dihydrochlorid 
• 75614-93-6 [3H]-(R)α-methylhistamine 

Relevant articles and documents

Design of Polymeric Inhibitors for the Control of Crystal Polymorphism. Induced Enantiomeric Resolution of Racemic Histidine by Crystallization at 25 deg C

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DESIGN OF STEREOSPECIFIC INHIBITORS FOR CRYSTAL DISSOLUTION

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.