Merck
All Photos(4)

H6034

Sigma-Aldrich

L-Histidine

suitable for cell culture, meets EP, USP testing specifications, from non-animal source

Synonym(s):
(S)-2-Amino-3-(4-imidazolyl)propionic acid, NSC 137773
Empirical Formula (Hill Notation):
C6H9N3O2
CAS Number:
Molecular Weight:
155.15
Beilstein:
84088
Número EC:
Número MDL:
eCl@ss:
32160406
ID de substância PubChem:
NACRES:
NA.26

fonte biológica

non-animal source

Nível de qualidade

200

Agency

meets EP testing specifications
meets USP testing specifications

teor

98.5-101.0%

forma

powder

technique(s)

cell culture | mammalian: suitable

Impurezas

endotoxin, tested

cor

white to off-white

pf

282 °C (dec.) (lit.)

solubilidade

H2O: 50 mg/mL

application(s)

peptide synthesis
pharmaceutical (small molecule)

SMILES string

N[C@@H](Cc1c[nH]cn1)C(O)=O

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

InChI key

HNDVDQJCIGZPNO-YFKPBYRVSA-N

Gene Information

human ... CA1(759) , CA2(760)

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Aplicação

L-histidine has been used as a component in agar plates containing 5-fluorocytosine (5-FC) for the selection of yeast transformants. It has also been used as a component of adult mouse keratinocyte growth medium.

Embalagem

10 mg in glass bottle
25, 100 g in poly bottle
1 kg in poly bottle

Ações bioquímicas/fisiológicas

L-Histidine is an essential amino acid that binds to metal ions and may aid in the transport of copper. Histidine is widely present at the active sites of enzymes. It also has a role in binding of heme groups, macromolecules and phosphate groups in the binding sites of proteins.
Precursor of histamine by action of histidine decarboxylase.

Código de classe de armazenamento

11 - Combustible Solids

WGK

WGK 1

Ponto de fulgor (ºF)

Not applicable

Ponto de fulgor (ºC)

Not applicable

Equipamento de proteção individual

Eyeshields, Gloves, type N95 (US)

Certificate of Analysis

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Certificate of Origin

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