L-Histidine - UltraBio™, ≥99.5%(NT) , CAS No.71-00-1

CAS: 71-00-1 Cat. No.: L755708 Formule: C₆H₉N₃O₂ Poids moléculaire: 155.15 Beilstein Registry Number: 84088 Numéro CE: 200-745-3

GRADE & PURITY UltraBio™, ≥99.5%(NT)

Storage

Room temperature

Shipped In

Normal

Vue d’ensemble

L-Histidine has been used for characterization of ZnO nanorod in an attempt to develop a technique for the ultra-low level detection of l-histidine.

Specifications

Spécifications et pureté

UltraBio™, ≥99.5%(NT)

Mécanismes biochimiques et physiologiques

Precursor of histamine by action of histidine decarboxylase.L-Histidine is involved in the one-carbon unit metabolism. It is associated with protein methylation. L-Histidine is a part of hemoglobin structure and function. L-Histidine is a component of dip

Conditions de stockage de stockage

Room temperature

Expédié en

Normal

Grade

UltraBio™

Pureté

≥99.5%(NT)

Noms et identifiants

Pubchem Sid

528765205

PH

7.0-8.0 (25 °C, 0.1 M in H 2 O)

Sourires canoniques

C1=C(NC=N1)CC(C(=O)O)N

IUPAC Name

(2S)-2-amino-3-(1H-imidazol-5-yl)propanoic acid

InChIKey

HNDVDQJCIGZPNO-YFKPBYRVSA-N

INCHI

1S/C6H9N3O2/c7-5(6(10)11)1-4-2-8-3-9-4/h2-3,5H,1,7H2,(H,8,9)(H,10,11)/t5-/m0/s1

Isomères SMILES

C1=C(NC=N1)C[C@@H](C(=O)O)N

WGK Allemagne

1

RTECS

MS3070000

CAS alternatif

71-00-1,26062-48-6

Termes d'entrée MeSH

Histidine;Histidine, L isomer;Histidine, L-isomer;L-Histidine;L-isomer Histidine

Poids moléculaire

155.15

Beilstein

84088

Reaxy-Rn

7800

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=7800&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic acids and derivatives
    • Classe Carboxylic acids and derivatives
      • Subclass Amino acids, peptides, and analogues
        • Level5 Amino acids and derivatives
          • Level6 Alpha amino acids and derivatives
            • Level7 Histidine and derivatives

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Classe: Carboxylic acids and derivatives
• Subclass: Amino acids, peptides, and analogues
• Intermediate Tree Nodes: Amino acids and derivatives - Alpha amino acids and derivatives
• Direct Parent: Histidine and derivatives
• Alternative Parents: L-alpha-amino acids Imidazolyl carboxylic acids and derivatives Aralkylamines Heteroaromatic compounds Amino acids Monocarboxylic acids and derivatives Carboxylic acids Azacyclic compounds Organopnictogen compounds Organic oxides Monoalkylamines Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aromatic heteromonocyclic compounds
• Substituents: Histidine or derivatives - Alpha-amino acid - L-alpha-amino acid - Imidazolyl carboxylic acid derivative - Aralkylamine - Azole - Imidazole - Heteroaromatic compound - Amino acid - Carboxylic acid - Azacycle - Organoheterocyclic compound - Monocarboxylic acid or derivatives - Organic nitrogen compound - Organooxygen compound - Organonitrogen compound - Primary amine - Primary aliphatic amine - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Carbonyl group - Organic oxygen compound - Amine - Aromatic heteromonocyclic compound
• Description: This compound belongs to the class of organic compounds known as histidine and derivatives. These are compounds containing cysteine or a derivative thereof resulting from reaction of cysteine at the amino group or the carboxy group, or from the replacement of any hydrogen of glycine by a heteroatom.
• External Descriptors: Common amino acids

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

Propriétés chimiques et physiques

• Solubilité: H 2 O: 0.1 M at 20 °C, clear, colorless
• Rotation spécifique [α]: 13 ° (C=11, 6mol/L HCl)
• Point de fusion (°C): 282°C
• Poids moléculaire: 155.150 g/mol
• XLogP3: -3.200
• Hydrogen Bond Donor Count: 3
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 3
• Exact Mass: 155.069 Da
• Monoisotopic Mass: 155.069 Da
• Topological Polar Surface Area: 92.000 Ų
• Heavy Atom Count: 11
• Formal Charge: 0
• Complexity: 151.000
• 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: 1