(S)-4-Aminovaleric acid

Base Information

Chemical Name:(S)-4-Aminovaleric acid
CAS No.:1558-59-4
Molecular Formula:C5H11NO2
Molecular Weight:117.148
Hs Code.:
UNII:G98ZJ0KD1D
DSSTox Substance ID:DTXSID301311352
Nikkaji Number:J80.229H
Wikidata:Q27278962
Metabolomics Workbench ID:1855
ChEMBL ID:CHEMBL284327
Mol file:1558-59-4.mol

Synonyms:(4S)-4-aminopentanoic acid;(S)-4-Aminovaleric acid;1558-59-4;(S)-4-Aminopentanoic acid;4S-aminopentanoic acid;(4S)-4-ammoniopentanoate;Pentanoic acid, 4-amino-, (S)-;4-Aminovaleric acid, (S)-;G98ZJ0KD1D;Pentanoic acid, 4-amino-, (4S)-;MFCD19203954;(S)-4-Aminopentanoicacid;D0N0ZK;UNII-G98ZJ0KD1D;SCHEMBL288484;CHEMBL284327;'(4S)-4-aminopentanoic acid';CHEBI:178407;DTXSID301311352;LMFA01100022;'(2E,4S)-4-aminopent-2-enoic acid;CS-0526945;EN300-1708022;Q27278962

Suppliers and Price of (S)-4-Aminovaleric acid

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

Total 10 raw suppliers

Chemical Property of (S)-4-Aminovaleric acid

Chemical Property:

Vapor Pressure:0.0123mmHg at 25°C
Melting Point:212-213 °C
Boiling Point:241°C at 760 mmHg
PKA:4.38±0.10(Predicted)
Flash Point:99.5°C
PSA：63.32000
Density:1.067g/cm³
LogP:0.89870
XLogP3:-2.7
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:3
Exact Mass:117.078978594
Heavy Atom Count:8
Complexity:82.5

Purity/Quality:: 98%+ ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(CCC(=O)O)N
Isomeric SMILES:C[C@@H](CCC(=O)O)N

Technology Process of (S)-4-Aminovaleric acid

There total 10 articles about (S)-4-Aminovaleric acid 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: 88.0%

: 123-76-2
levulinic acid

: 1558-59-4
(S)-4-Aminovaleric acid

Guidance literature:: With formate dehydrogenase from Candida boidinii; amine dehydrogenase from Petrotoga mobilis; NADH; In aq. buffer; at 50 ℃; for 24h; pH=8.5; Reagent/catalyst; Temperature; pH-value; enantioselective reaction; Catalytic behavior; Enzymatic reaction;
DOI:10.1039/c6cy01625a

Reference yield:

: 2627-86-3
(S)-1-phenyl-ethylamine

: 123-76-2
levulinic acid

: 1558-59-4
(S)-4-Aminovaleric acid

: 98-86-2
acetophenone

Guidance literature:: With pyridoxal 5'-phosphate; recombinant ω-transaminase from Burkholderia vietnamiensis G4; In aq. phosphate buffer; at 37 ℃; for 12h; pH=7.4; Time; enantioselective reaction; Enzymatic reaction;
DOI:10.1016/j.molcatb.2013.11.013