L-Homoserine

Names

[ 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

Biological Activity

[Description]:

H-D-Homoser-OH is a biochemical reagent that can be used as a biological material or organic compound for life science related research.

[Related Catalog]:

Research Areas >> Others

Signaling Pathways >> Others >> Others

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

Click to get detail 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

Click to get detail synthetic route

Precursor & DownStream

Precursor

DownStream

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...

Related Compounds

The content on this webpage is sourced from various professional data sources. If you have any questions or concerns regarding the content, please feel free to contact service1@chemsrc.com.