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Catalog | BBC71001 |
CAS | 71-00-1 |
Structure | ![]() |
Description | Histidine (abbreviated as His or H; encoded by the codons CAU and CAC) is an α-amino acid that is used in the biosynthesis of proteins. It contains an α-amino group (which is in the protonated –NH3+ form under biological conditions), a carboxylic acid group (which is in the deprotonated –COO− form under biological conditions), and a side chain imidazole, classifying it as a positively charged amino acid at physiological pH. Initially thought essential only for infants, longer-term studies have shown it is essential for adults also.Histidine was first isolated by German physician Albrecht Kossel and Sven Hedin in 1896. It is also a precursor to histamine, a vital inflammatory agent in immune responses. The acyl radical is histidyl. |
Synonyms | 4-(2-Amino-2-carboxyethyl)imidazole |
IUPAC Name | (2S)-2-Amino-3-(1H-imidazol-5-yl)propanoic acid |
Molecular Weight | 155.15 |
Molecular Formula | C6H9N3O2 |
Canonical SMILES | C1=C(NC=N1)CC(C(=O)O)N |
InChI | 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 |
Boiling Point | 278.95 °C |
Melting Point | 282 °C(lit.) |
Flash Point | 282ºC |
Purity | 99% |
Density | 1.3092 g/cm³ |
Solubility | Soluble in water, insoluble in ether |
Appearance | Solid |
Storage | 2-8 °C |
Active Content | 95% |
EC Number | 225-660-9 |
pH | 7-8.5 |
pKa | 1.8(at 25 °C) |
Refractive Index | 1.731 |
Solubility in Water | 41.6 g/L (25 ºC) |
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