L-Pentahomoserine

Base Information

Chemical Name:L-Pentahomoserine
CAS No.:6152-89-2
Molecular Formula:C5H11 N O3
Molecular Weight:133.147
Hs Code.:2922509090
UNII:4U1FH45CS8
Nikkaji Number:J1.289.756A
Wikidata:Q27094062
Metabolomics Workbench ID:147642
ChEMBL ID:CHEMBL495224
Mol file:6152-89-2.mol

Synonyms:2-amino-5-hydroxypentanoic acid;2-amino-5-hydroxyvaleric acid;2-amino-5-hydroxyvaleric acid, (DL)-isomer;2-amino-5-hydroxyvaleric acid, (L)-isomer;5-hydroxy-2-aminovalerate;5-hydroxy-2-aminovaleric acid;5-hydroxynorvaline;5-OH-2-NH2-valerate;alpha-amino-delta-hydroxyvaleric acid;HAVA-5 cpd

Suppliers and Price of L-Pentahomoserine

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

Crysdot
(S)-2-Amino-5-hydroxypentanoicacid 98%
1g
$ 743.00

Chemenu
(S)-2-amino-5-hydroxypentanoicacid 98%
1g
$ 701.00

Activate Scientific
(S)-2-Amino-5-hydroxypentanoic acid HCl 95% ee
1 g
$ 804.00

Acrotein
(S)-2-Amino-5-hydroxypentanoicacid 97%
1g
$ 660.00

Total 12 raw suppliers

Chemical Property of L-Pentahomoserine

Chemical Property:

Vapor Pressure:7.36E-05mmHg at 25°C
Boiling Point:306.1°C at 760 mmHg
PKA:2.51±0.24(Predicted)
Flash Point:138.9°C
PSA：83.55000
Density:1.241g/cm³
LogP:-0.12890
Storage Temp.:2-8°C
XLogP3:-4.2
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:4
Exact Mass:133.07389321
Heavy Atom Count:9
Complexity:94.2

Purity/Quality:

97% ^*data from raw suppliers

(S)-2-Amino-5-hydroxypentanoicacid 98% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

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

Technology Process of L-Pentahomoserine

There total 2 articles about L-Pentahomoserine 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:

: 1499-55-4
L-glutamic acid 5-methyl ester

: 6152-89-2
(S)-5-hydroxy-2-aminovaleric acid

: 147-85-3,25191-13-3,37159-97-0,4305-67-3,4607-28-7
L-proline

Guidance literature:: L-glutamic acid 5-methyl ester; With lithium borohydride; In tetrahydrofuran; Inert atmosphere; Reflux;

With water; acetic acid; In tetrahydrofuran; methanol; pH=5; Cooling with ice;
DOI:10.1016/j.phytochem.2009.03.001

Reference yield:

: 70-26-8,25104-12-5,410523-47-6
L-ornithine

: 16814-81-6
(S)-2-hydroxy-5-aminopentanoic acid

: 6152-89-2
(S)-5-hydroxy-2-aminovaleric acid

Guidance literature:: With hydrogenchloride; sodium nitrite; In water; for 24h; Ambient temperature; NaNO₂: 1 equivalent;

Reference yield:

: 6152-89-2
(S)-5-hydroxy-2-aminovaleric acid

: 147-85-3,25191-13-3,37159-97-0,4305-67-3,4607-28-7
L-proline

Guidance literature:: (S)-5-hydroxy-2-aminovaleric acid; With NosE gene from Escherichia coli; NAD; zinc(II) sulfate; glycine; In water; at 42 ℃; for 5h; pH=10;

With NosF gene from Escherichia coli; In water; for 0.25h; pH=10; Further stages.;
DOI:10.1021/jo026479q