H7750

DL-Histidine

≥99% (TLC), suitable for ligand binding assays

Manufacturer: Sigma Aldrich

CAS Number: 4998-57-6

Synonym(S): (±)-2-Amino-3-(4-imidazolyl)propionic acid

Select a Size

Pack Size SKU Availability Price
25 G H7750-25-G In Stock ₹ 21,834.03
100 G H7750-100-G In Stock ₹ 48,939.83

H7750 - 25 G

₹ 21,834.03

In Stock

Quantity

1

Base Price: ₹ 21,834.03

GST (18%): ₹ 3,930.125

Total Price: ₹ 25,764.155

Quality Level

200

Assay

≥99% (TLC)

form

powder

technique(s)

ligand binding assay: suitable

mp

273 °C (dec.) (lit.)

solubility

0.5 M HCl: soluble

application(s)

peptide synthesis

SMILES string

NC(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)

InChI key

HNDVDQJCIGZPNO-UHFFFAOYSA-N

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Description

  • Application: DL-Histidine has been used to study the fouling behaviour of polyethersulfone ultrafiltration membranes made with different PVP (polyvinylpyrrolidone).[1]
  • Biochem/physiol Actions: 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 dipeptides with antioxidative property. Histidine serves as a precursor for the formation of histamine, which is associated with allergic responses. Urocanic acid, an immune response modulator in skin is also biosynthesised from histidine.[2]

SAFETY INFORMATION

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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≥99% (TLC), suitable for ligand bin...


Quality Level:
200

Assay:
≥99% (TLC)

form:
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technique(s):
ligand binding assay: suitable

mp:
273 °C (dec.) (lit.)

solubility:
0.5 M HCl: soluble

application(s):
peptide synthesis

SMILES string:
NC(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)

InChI key:
HNDVDQJCIGZPNO-UHFFFAOYSA-N

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CN[C@H]1C[C@@H](N)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@@H]3O[C@]4(O[C@H]([C@H](N)CO)[C@H](O)[C@H](O)[C@H]4O)O[C@H]23)[C@@H]1O

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