L-histidinol

Base Information

Chemical Name:L-histidinol
CAS No.:4836-52-6
Molecular Formula:C6H11N3O
Molecular Weight:141.173
Hs Code.:
DSSTox Substance ID:DTXSID50863460
Nikkaji Number:J80.912H
Wikidata:Q27101817
Pharos Ligand ID:MM1Q63ZACVJR
Metabolomics Workbench ID:38331
ChEMBL ID:CHEMBL278081
Mol file:4836-52-6.mol

Synonyms:Histidinol;Histidol

Suppliers and Price of L-histidinol

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Chemenu
(2S)-2-Amino-3-(1H-imidazol-5-yl)propan-1-ol 95%+
10g
$ 288.00

Chemenu
(2S)-2-Amino-3-(1H-imidazol-5-yl)propan-1-ol 95%+
5g
$ 175.00

Chemenu
(2S)-2-Amino-3-(1H-imidazol-5-yl)propan-1-ol 95%+
1g
$ 54.00

American Custom Chemicals Corporation
HISTIDINOL 95.00%
5MG
$ 505.67

Total 8 raw suppliers

Chemical Property of L-histidinol

Chemical Property:

Vapor Pressure:4.34E-09mmHg at 25°C
Melting Point:197-199.5℃
Boiling Point:455.5°Cat760mmHg
PKA:12.63±0.10(Predicted)
Flash Point:229.3°C
PSA：74.93000
Density:1.261g/cm³
LogP:-0.02790
XLogP3:-1.2
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:3
Exact Mass:141.090211983
Heavy Atom Count:10
Complexity:99

Purity/Quality:

97% ^*data from raw suppliers

(2S)-2-Amino-3-(1H-imidazol-5-yl)propan-1-ol 95%+ ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=C(NC=N1)CC(CO)N
Isomeric SMILES:C1=C(NC=N1)C[C@@H](CO)N

Technology Process of L-histidinol

There total 7 articles about L-histidinol which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

: 25679-93-0
L-histidinol 1-phosphate

: 4836-52-6
(S)-histidinol

Guidance literature:: With L-histidinol-phosphatephosphohydrolase; In water; Enzymatic reaction;
DOI:10.1021/acs.biochem.9b00579

Reference yield:

: 1499-46-3
L-Histidine methyl ester

: 4836-52-6
(S)-histidinol

Guidance literature:: With lithium aluminium tetrahydride; In tetrahydrofuran; for 3h; Yield given; Heating;
DOI:10.1002/ardp.19803130810

Reference yield:

: 645-35-2
L-histidine monohydrochloride

: 4836-52-6
(S)-histidinol

Guidance literature:: Multi-step reaction with 2 steps

1: 95 percent / HCl / 3 h / Heating

2: LiAlH₄ / tetrahydrofuran / 3 h / Heating

With hydrogenchloride; lithium aluminium tetrahydride; In tetrahydrofuran;
DOI:10.1002/ardp.19803130810