![L-Histidine monohydrochloride monohydrat [5934-29-2] L-Histidine monohydrochloride monohydrat [5934-29-2]](https://www.targetmol.com/group3/M00/37/E3/CgoaEGayUziEGbIxAAAAAKKSKOI808.png)
L-Histidine monohydrochloride monohydrat [5934-29-2]
T4826
CAS Number5934-29-2
Product group Chemicals
Molecular Weight209.63
Overview
- SupplierTargetMol Chemicals
- Product NameL-Histidine monohydrochloride monohydrat
- Delivery Days Customer4
- CAS Number5934-29-2
- Category SupplierChemical
- CertificationResearch Use Only
- Chemical NameL-Histidine monohydrochloride monohydrat
- Molecular FormulaC6H12ClN3O3
- Molecular Weight209.63
- Scientific DescriptionHistidine (abbreviated as His or H) is an alpha-amino acid. The L-isomer is one of the 22 proteinogenic amino acids, i.e., the building blocks of proteins. It is classified as a charged, polar because of the hydrophilic nature of the imidazole side chain. L-Histidine is a positively charged (pKa 6.5) aromatic amino acid. Histidine residues are often found in enzyme active sites, where the chemistry of the imidazole ring of histidine makes it a nucleophile and a good acid/base catalyzer. Histidine is special in that its biosynthesis is inherently linked to the pathways of nucleotide formation. In the first step of histidine synthesis, PRPP (5-phosphoribosyl-alpha-pyrophosphate) condenses with ATP to form a purine, N1-5-phosphoribosyl ATP, in a reaction that is driven by the subsequent hydrolysis of the pyrophosphate that condenses out. Glutamine plays a role as an amino group donor resulting in the formation of 5-aminoamidazole-4-carboximide ribonucleotide (ACAIR), which is an intermediate in purine biosynthesis. Hisitidne is catabolized by the enzyme histidine ammonia-lyase which converts histidine into ammonia and urocanic acid.
- Shelf life instruction3 years
- SMILESO.Cl.NC(Cc1c[nH]cn1)C(O)=O
- Storage Instruction-20°C
- UNSPSC12352209