L-Homoserin
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- CAS-Nr.
- 672-15-1
- Bezeichnung:
- L-Homoserin
- Englisch Name:
- L-Homoserine
- Synonyma:
- HOMOSERINE;HSE;(S)-2-AMINO-4-HYDROXYBUTANOIC ACID;H-HOMOSER-OH;H-HSE-OH;H-HOSER-OH;H-HOMOSERINE;(2S)-2-Amino-4-hydroxybutanoic acid;RODH;SDR9C6
- CBNumber:
- CB2854094
- Summenformel:
- C4H9NO3
- Molgewicht:
- 119.12
- MOL-Datei:
- 672-15-1.mol
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L-Homoserin Eigenschaften
- Schmelzpunkt:
- 203 °C (dec.)(lit.)
- Siedepunkt:
- 222.38°C (rough estimate)
- alpha
- -8.5 º (c=2, H2O 22 ºC)
- Dichte
- 1.3126 (rough estimate)
- Brechungsindex
- 1.4183 (estimate)
- storage temp.
- Store below +30°C.
- Löslichkeit
- 1100g/l
- Aggregatzustand
- Crystalline Powder
- pka
- 2.71(at 25℃)
- Farbe
- White to light yellow
- Wasserlöslichkeit
- 1100 g/L (30 ºC)
- Merck
- 14,4739
- BRN
- 1721681
- InChIKey
- UKAUYVFTDYCKQA-VKHMYHEASA-N
- LogP
- -1.289 (est)
- CAS Datenbank
- 672-15-1(CAS DataBase Reference)
L-Homoserin Chemische Eigenschaften,Einsatz,Produktion Methoden
S-Sätze Betriebsanweisung:
S24/25:Berührung mit den Augen und der Haut vermeiden.
Chemische Eigenschaften
white to light yellow crystalline powder
Verwenden
L-Homoserine is used in the biosynthesis of methionine, threonine and isoleucine. It is also used as an internal standard for neurotransmitter analysis and amino acids quantification.
Definition
ChEBI: L-homoserine is the L-enantiomer of homoserine. It has a role as a human metabolite, an algal metabolite, a Saccharomyces cerevisiae metabolite and an Escherichia coli metabolite. It is an enantiomer of a D-homoserine. It is a tautomer of a L-homoserine zwitterion.
Allgemeine Beschreibung
L-Homoserine is a variant of serine with an additional carbon on its side chain.
Biochem/physiol Actions
L-Homoserine is synthesized by deoxidation process, catalysed by homoserine dehydrogenase. This is one of the steps in the synthesis of L-threonine. The carbon flux in in bacteria such as E. coli is maintained by this reaction.
läuterung methode
Likely impurities are N-chloroacetyl-L-homoserine, N-chloroacetyl-D-homoserine, L-homoserine, homoserine lactone, homoserine anhydride (formed in strong solutions of homoserine if slightly acidic). It cyclises to the lactone in strongly acidic solution. It crystallises from water by adding 9 volumes of EtOH. [Greenstein & Winitz The Chemistry of the Amino Acids J. Wiley, Vol 3 pp 2612-2616 1961, Beilstein 4 IV 3187.]
L-Homoserin Upstream-Materialien And Downstream Produkte
Upstream-Materialien
Downstream Produkte
L-Homoserin Anbieter Lieferant Produzent Hersteller Vertrieb Händler.
Global( 455)Lieferanten
672-15-1(L-Homoserin)Verwandte Suche:
- (S)-(-)-2-AMINO-4-HYDROXYBUTYRIC ACID
- (S)-2-AMINO-4-HYDROXYBUTYRIC ACID
- L-2-AMINO-4-HYDROXYBUTANOIC ACID
- L-2-AMINO-4-HYDROXYBUTYRIC ACID
- L-2-AMINO-4-HYDROXYBUTYRIC ACID HYDROCHLORIDE
- H-L-HSE-OH
- H-HOSER-OH HCL
- HOMOSERINE-L
- 2-AMINO-4-HYDROXYBUTYRIC ACID
- L-2-Amino-4-hydroxybutyricacid=H-Hser-OH
- (S)-Homeserine
- HOMOSERINE, (S)-2-AMINO-4-HYDROXYBUTYRIC ACID
- L-Homoserine, (S)-2-Amino-4-hydroxybutyric acid
- H-HOSER-OHCL
- L-Beta-Homo-Ser
- H-HoSer-OHCl;H-HoSer-OHCl
- L-Homoserine,97%
- (S)-2-Amino-4-hydroxybutyric acid Hse
- (S)-2-Amino-4-hydroxybutyric acid Hse H-HoSer-OH
- H-Hser-OH ,98%
- L-Homoserine
- NSC 206251
- L-(-)-HOMOSERINE FOR SYNTHESIS
- L-HoMoserine, 95+%
- HSD17B6
- RODH
- SDR9C6
- L-Homoserine, >=98%
- L-Homoserine 98%
- L-Homoserine>
- L-Homoserine USP/EP/BP
- laevo-homoserine
- (2S)-2-azaniumyl-4-hydroxybutanoate
- L-Homoserine 672-15-1
- H-HSE-OH
- H-HOSER-OH
- H-HOMOSER-OH
- H-HOMOSERINE
- HSE
- HOMOSERINE
- (S)-2-AMINO-4-HYDROXYBUTANOIC ACID
- (2S)-2-Amino-4-hydroxybutanoic acid
- L-Homoserine (9CI, ACI)
- (2S)-2-amino-4-hydroxybutanoic acid (homoserine)
- Lysine Impurity 12 (L-?Homoserine)
- Carisoprodol Impurity 3 (Carisoprodol EP Impurity C)
- 672-15-1
- 6-00-6
- 627-15-1
- HOCH2CH2CHNH2COOH
- Amino Acid Library
- BioChemical
- Homo-Amino Acids
- Metabolomics
- Metabolic Libraries
- Peptide Synthesis
- Specialty Synthesis
- Unnatural Amino Acid Derivatives
