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Thermo Scientific Chemicals L-Histidine monohydrochloride monohydrate, 99%

L-Histidine monohydrochloride monohydrate, CAS # 5934-29-2, is a histidine precursor through histidine decarboxylase.

42.61 € - 261.30 €

Chemical Identifiers

CAS 5934-29-2
Molecular Formula C6H12ClN3O3
Molecular Weight (g/mol) 209.63
MDL Number MFCD00151027
InChI Key CMXXUDSWGMGYLZ-XRIGFGBMSA-N
Synonym l-histidine hydrochloride hydrate, l-histidine hydrochloride monohydrate, s-2-amino-3-1h-imidazol-4-yl propanoic acid hydrochloride hydrate, h-his-oh.hcl.h2o, l-histidine monohydrochloride monohydrate, l-histidine, monohydrochloride, monohydrate, l-histidin hydrate hydrochloride, histidine, monohydrochloride, monohydrate, l, h-his-ohhclh2o, l-histidine, hydrochloride, monohydrate
PubChem CID 165377
IUPAC Name (2S)-2-amino-3-(1H-imidazol-5-yl)propanoic acid;hydrate;hydrochloride
SMILES C1=C(NC=N1)CC(C(=O)O)N.O.Cl
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Thermo Scientific Chemicals
A17627.18
50 g
42.61 €
50g
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Thermo Scientific Chemicals
A17627.30
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A17627.36
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Description

Description

L-Histidine monohydrochloride monohydrate is used as a precursor through histidine decarboxylase. It is also used to study the cultures of the human T-lymphoblastic leukemia cell line, modulation of apoptosis. It is also used to enhance the biosynthesis of Lovastatin by cultured aspergillus terreus. It is utilized as a single nitrogen source to probe swarming in Pseudomonas aeruginosa on agar. It is employed as a component to avoid the risk of contaminating bioproducts with adventitious viruses.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

General Description

• L-Histidine monohydrochloride monohydrate is a histidine precursor via histidine decarboxylase.

Application

• As a precursor of histidine, it can be used to enhance the biosyntyhesis of lovastatin by cultured Aspergillus terreus
• It is utilized as a single nitrogen source to probe swarming in Pseudomonas aeruginosa on agar
• It can be employed in laboraotry applications as a component to avoid the risk of contaminating bioproducts with adventitious viruses
• It is also used for laboratory study of cultures of the human T-lymphoblastic leukemia cell line, and modulation of apoptosis

Specifications

Chemical Identifiers

5934-29-2
209.63
CMXXUDSWGMGYLZ-XRIGFGBMSA-N
165377
C1=C(NC=N1)CC(C(=O)O)N.O.Cl
C6H12ClN3O3
MFCD00151027
l-histidine hydrochloride hydrate, l-histidine hydrochloride monohydrate, s-2-amino-3-1h-imidazol-4-yl propanoic acid hydrochloride hydrate, h-his-oh.hcl.h2o, l-histidine monohydrochloride monohydrate, l-histidine, monohydrochloride, monohydrate, l-histidin hydrate hydrochloride, histidine, monohydrochloride, monohydrate, l, h-his-ohhclh2o, l-histidine, hydrochloride, monohydrate
(2S)-2-amino-3-(1H-imidazol-5-yl)propanoic acid;hydrate;hydrochloride

Specifications

∽240°C (decomposition)
99%
MFCD00151027
14,4720
Soluble in water.
C1=C(NC=N1)CC(C(=O)O)N.O.Cl
209.63
209.63 (191.62 anhydrous)
L-Histidine Monohydrochloride Monohydrate
5934-29-2
C6H12ClN3O3
4168261
l-histidine hydrochloride hydrate, l-histidine hydrochloride monohydrate, s-2-amino-3-1h-imidazol-4-yl propanoic acid hydrochloride hydrate, h-his-oh.hcl.h2o, l-histidine monohydrochloride monohydrate, l-histidine, monohydrochloride, monohydrate, l-histidin hydrate hydrochloride, histidine, monohydrochloride, monohydrate, l, h-his-ohhclh2o, l-histidine, hydrochloride, monohydrate
CMXXUDSWGMGYLZ-XRIGFGBMSA-N
(2S)-2-amino-3-(1H-imidazol-5-yl)propanoic acid;hydrate;hydrochloride
165377
99%
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Safety and Handling

Safety and Handling

missing translation for 'einecsNumber' : 211-438-9

missing translation for 'rtecsNumber' : MS3119000

missing translation for 'tsca' : Yes

Recommended Storage : Ambient temperatures

SDS
Documents

Documents

Product Certifications

RUO – Research Use Only

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