H6034

L-Histidine

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

• Sinónimos: NSC 137773, (S)-2-Amino-3-(4-imidazolyl)propionic acid
• Empirical Formula (Hill Notation): C₆H₉N₃O₂
• Número de CAS: 71-00-1
• Peso molecular: 155.15
• Beilstein: 84088
• Número de EC: 200-745-3
• Número MDL: MFCD00064315
• eCl@ss: 32160406
• ID de la sustancia en PubChem: 24895728
• NACRES: NA.26

Propiedades

• Nivel de calidad: 200
• origen biológico: non-animal source
• Agency: meets EP testing specifications; meets USP testing specifications
• ensayo: 98.5-101.0%
• formulario: powder
• technique(s): cell culture | mammalian: suitable
• impurezas: endotoxin, tested
• color: white to off-white
• mp: 282 °C (dec.) (lit.)
• solubilidad: 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)

Descripción

Aplicación

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.

Envase

10 mg in glass bottle

25, 100 g in poly bottle

1 kg in poly bottle

Acciones bioquímicas o 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.

Información de seguridad

• Código de clase de almacenamiento: 11 - Combustible Solids
• WGK: WGK 1
• Punto de inflamabilidad F: Not applicable
• Punto de inflamabilidad C: Not applicable
• Equipo de protección personal: Eyeshields, Gloves, type N95 (US)