Histidine hydrochloride hydrate

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Names

[ CAS No. ]:
123333-71-1

[ Name ]:
Histidine hydrochloride hydrate

[Synonym ]:
l-histidine mono hydrochloride monohydrate
Histidine hydrochloride hydrate
(2S)-2-amino-3-(1H-imidazol-5-yl)propanoic acid hydrate hydrochloride
L-histidine, hydrochloride, hydrate
L-histidine, monohydrochloride, monohydrate
Histidine, hydrochloride, hydrate (1:1:1)
MFCD00064555
DL-Histidine monohydrochloride monohydrate
(S)-2-Amino-3-(1H-imidazol-4-yl)propanoic acid hydrochloride hydrate
L-HISTIDINE monohydrochloride MONOHYDRATE
EINECS 229-266-8
L-Histidine Hydrochloride Monohydrate

Chemical & Physical Properties

[ Boiling Point ]:
458.9ºC at 760mmHg

[ Melting Point ]:
253ºC (dec.)

[ Molecular Formula ]:
C6H12ClN3O3

[ Molecular Weight ]:
209.631

[ Flash Point ]:
231.3ºC

[ Exact Mass ]:
209.056717

[ PSA ]:
101.23000

[ LogP ]:
0.80210

[ Vapour Pressure ]:
3.25E-09mmHg at 25°C

[ Water Solubility ]:
H2O: 0.1 g/mL, clear | 0.1 G/ML

MSDS

Click to get detail MSDS

Safety Information

[ Personal Protective Equipment ]:
Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter

[ Hazard Codes ]:
Xn

[ Risk Phrases ]:
22-36/37/38

[ Safety Phrases ]:
S24/25

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

Articles

Quantification of plasma lactate concentrations using capillary electrophoresis with contactless conductivity detection.

Electrophoresis 32 , 884-889, (2011)

The quantification of plasma lactate and evaluation of the lactate threshold by CE with capacitively coupled contactless conductivity is demonstrated. The only sample preparation needed was deproteini...

Amino acid ionic liquids as chiral ligands in ligand-exchange chiral separations.

Chemistry 15 , 9889-9896, (2009)

Recently, amino acid ionic liquids (AAILs) have attracted much research interest. In this paper, we present the first application of AAILs in chiral separation based on the chiral ligand exchange prin...


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Related Compounds

  • Histidine hydrochloride hydrate
  • Histidine hydrochloride
  • histidine hydrochloride
  • Valacyclovir hydrochloride hydrate
  • Topotecan hydrochloride hydrate
  • BIX01294 (hydrochloride hydrate)
  • 4-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-4-({2-[methyl(propyl)amino]ethyl}carbamoyl)butanoic acid
  • 3-cyclopropyl-4-[3-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-2,2-dimethylpropanamido]butanoic acid
  • 2-[3-cyclopropyl-4-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)butanamido]-3-methoxy-2-methylpropanoic acid
  • (3S)-3-{2-[1-benzyl-4-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)piperidin-4-yl]acetamido}pentanoic acid
  • (3S)-3-[3-cyclopropyl-3-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)butanamido]butanoic acid
  • (3S)-3-{[3-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)furan-2-yl]formamido}butanoic acid
  • (3S)-3-{2-[1-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)cyclopropyl]acetamido}butanoic acid
  • 1-[4-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-2,2-dimethylbutanoyl]-4-methylpiperidine-3-carboxylic acid
  • (2R)-1-[1-benzyl-3-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)pyrrolidine-3-carbonyl]pyrrolidine-2-carboxylic acid
  • 4-{[1-benzyl-4-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)piperidin-4-yl]formamido}-3-hydroxybutanoic acid
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