L-Homoserine

Suppliers

Names

[ CAS No. ]:
6027-21-0

[ Name ]:
L-Homoserine

[Synonym ]:
Homoserine
(2R)-2-amino-4-hydroxybutanoic acid
(2S)-2-Amino-4-hydroxybutyric Acid
(S)-2-amino-4-hydroxy-Butanoic acid
(R)-homoserine
(S)-Homoserine
(R)-3-amino-5-hydroxypentanoic acid
(R)-(+)-2-Amino-4-hydroxybutyric acid
Homoserine,D
MFCD00077786
AmbotzHAA1028
H-D-HoSer-OH
R-2-Amino-4-hydroxybutyric acid (D-Homoser)
D-Homoserine
(S)-2-Amino-4-hydroxybutanoic acid

Chemical & Physical Properties

[ Density]:
1.3±0.1 g/cm3

[ Boiling Point ]:
368.7±32.0 °C at 760 mmHg

[ Melting Point ]:
205ºC

[ Molecular Formula ]:
C4H9NO3

[ Molecular Weight ]:
119.12

[ Flash Point ]:
176.8±25.1 °C

[ Exact Mass ]:
119.058243

[ PSA ]:
83.55000

[ LogP ]:
-1.13

[ Vapour Pressure ]:
0.0±1.9 mmHg at 25°C

[ Index of Refraction ]:
1.511

[ Storage condition ]:
2~8°C

MSDS

Safety Information

[ Personal Protective Equipment ]:
Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter

[ Hazard Codes ]:
Xi

[ Safety Phrases ]:
S24/25

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2922509090

Synthetic Route

Precursor & DownStream

Precursor

  • (2R)-methionine methysulfonium iodide
  • 3-AMINO-3-(FURAN-2-YL)PROPAN-1-OL
  • D-Homoserine Lactone hydrochloride
  • D-methionine
  • 2(3H)-Furanone,3-aminodihydro-,(3R)-(9CI)
  • Cbz-D-Homoserine lactone

DownStream

  • N-[(Benzyloxy)carbonyl]-D-homoserine
  • Cbz-D-Homoserine lactone

Customs

[ HS Code ]: 2922509090

[ Summary ]:
2922509090. other amino-alcohol-phenols, amino-acid-phenols and other amino-compounds with oxygen function. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

Articles

A Simple Enzymatic Method for Production of a Wide Variety of D-Amino Acids Using L-Amino Acid Oxidase from Rhodococcus sp. AIU Z-35-1.

Enzyme Res. 2010 , 567210., (2010)

A simple enzymatic method for production of a wide variety of D-amino acids was developed by kinetic resolution of DL-amino acids using L-amino acid oxidase (L-AAO) with broad substrate specificity fr...

Engineering d-amino acid containing novel protease inhibitors using catalytic site architecture.

Bioorg. Med. Chem. 14 , 214-236, (2006)

The mechanism of proteolysis by serine proteases is a reasonably well-understood process. Typically, a histidine residue acting as a general base deprotonates the catalytic serine residue and the hydr...

Structure of the O-antigen of Acinetobacter lwoffii EK30A; identification of d-homoserine, a novel non-sugar component of bacterial polysaccharides.

Org. Biomol. Chem. 8 , 3571-3577, (2010)

We established a peculiar structure of the O-specific polysaccharide (O-antigen) of a psychrotrophic strain of Acinetobacter lwoffii, EK30A, isolated from a 1.6-1.8 million-year-old Siberian permafros...


More Articles


Related Compounds

  • L-Homoserine
  • L-Homoserine
  • L-Homoserine
  • L-homoserine
  • L-Homoserine
  • Cbz-L-Homoserine