L-Histidinol dihydrochloride - 10mM in DMSO , CAS No.1596-64-1

CAS: 1596-64-1 Cat. No.: L421910 Molecular Weight: 214.09 Beilstein Registry Number: 3914853 EC Number: 216-482-2

GRADE & PURITY 10mM in DMSO

Synonyms

FRCAFNBBXRWXQA-XRIGFGBMSA-N | L-Histidinol dihydrochloride, >=98 (TLC) | HY-W014233 | MFCD00078058 | 8,10-DIAZA-6-HYDROXY-5-METHYLENE-1-(2-METHYL-1,2,3-TRIHYDROXYPROPYL)-2-OXABICYCLO(4.2.2)DECAN-7,9-DIONE | EINECS 216-482-2 | l-histidinol 2hcl | CHEBI:135

Storage

Store at -80°C

Shipped In

Dry ice packs + Cold packs

Overview

Precursor of histamine,reversible inhibitor of protein synthesis.

Specifications

Synonyms

FRCAFNBBXRWXQA-XRIGFGBMSA-N | L-Histidinol dihydrochloride, >=98 (TLC) | HY-W014233 | MFCD00078058 | 8, 10-DIAZA-6-HYDROXY-5-METHYLENE-1-(2-METHYL-1, 2, 3-TRIHYDROXYPROPYL)-2-OXABICYCLO(4.2.2)DECAN-7, 9-DIONE | EINECS 216-482-2 | l-histidinol 2hcl | CHEBI:135

Specifications & Purity

10mM in DMSO

Storage

Store at -80°C

Shipped In

Dry ice packs + Cold packs

This product requires cold chain shipping. Ground and other economy services are not available.

Names and Identifiers

• Canonical Smiles: C1=C(NC=N1)CC(CO)N.Cl.Cl
• IUPAC Name: (2S)-2-amino-3-(1H-imidazol-5-yl)propan-1-ol;dihydrochloride
• InChIKey: FRCAFNBBXRWXQA-XRIGFGBMSA-N
• INCHI: 1S/C6H11N3O.2ClH/c7-5(3-10)1-6-2-8-4-9-6;;/h2,4-5,10H,1,3,7H2,(H,8,9);2*1H/t5-;;/m0../s1
• Isomeric SMILES: C1=C(NC=N1)C[C@@H](CO)N.Cl.Cl
• WGK Germany: 3
• RTECS: NI8260000
• Alternate CAS: 4836-52-6
• Molecular Weight: 214.09
• Beilstein: 3914853

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic nitrogen compounds
    • Class Organonitrogen compounds
      • Subclass Amines

• Kingdom: Organic compounds
• Superclass: Organic nitrogen compounds
• Class: Organonitrogen compounds
• Subclass: Amines
• Intermediate Tree Nodes: Not available
• Direct Parent: Aralkylamines
• Alternative Parents: Imidazoles Heteroaromatic compounds 1,2-aminoalcohols Azacyclic compounds Primary alcohols Organopnictogen compounds Monoalkylamines Hydrochlorides Hydrocarbon derivatives
• Molecular Framework: Aromatic heteromonocyclic compounds
• Substituents: Aralkylamine - Azole - Imidazole - Heteroaromatic compound - 1,2-aminoalcohol - Organoheterocyclic compound - Azacycle - Organic oxygen compound - Primary amine - Primary alcohol - Organooxygen compound - Primary aliphatic amine - Hydrocarbon derivative - Organopnictogen compound - Alcohol - Hydrochloride - Aromatic heteromonocyclic compound
• Description: This compound belongs to the class of organic compounds known as aralkylamines. These are alkylamines in which the alkyl group is substituted at one carbon atom by an aromatic hydrocarbyl group.
• External Descriptors: Not available

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Chemical and Physical Properties

• Sensitivity: Moisture sensitive.
• Molecular Weight: 214.090 g/mol
• Hydrogen Bond Donor Count: 5
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 3
• Exact Mass: 213.044 Da
• Monoisotopic Mass: 213.044 Da
• Topological Polar Surface Area: 74.900 Ų
• Heavy Atom Count: 12
• Formal Charge: 0
• Complexity: 99.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 1
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 3

XLogP3

References

1. Shuping Fei, Jiatong Zhao, Wenwen Wu, Chaoqun Lian, Wanggang Tang.  (2025)  Biochemical characterization of histidinol dehydrogenase from the human pathogen Neisseria gonorrhoeae.  PROTEIN EXPRESSION AND PURIFICATION,      [PMID:41016688] [10.1016/j.pep.2025.106824]