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DL-GAMMA-AMINO-B-HYDROXYBUTYRIC ACIDCRYS TALLINE

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DL-GAMMA-AMINO-B-HYDROXYBUTYRIC ACIDCRYS TALLINE Basic information

Product Name:
DL-GAMMA-AMINO-B-HYDROXYBUTYRIC ACIDCRYS TALLINE
Synonyms:
  • (3R)-4-ammonio-3-hydroxybutanoate
  • Aminohydroxybutyric
  • DL-G-AMINO-B-HYDROXYBUTYRICACID
  • (+-)-3-Hydroxy-4-aminobutanoic acid
  • (RS)-3-Hydroxy-γ-aminobutyric acid
  • (RS)-4-Amino-3-hydroxybutanoic acid
  • (RS)-γ-Amino-β-hydroxybutyric acid
  • 3-Hydroxy-4-aminobutanoic acid
CAS:
924-49-2
MF:
C4H9NO3
MW:
119.12
EINECS:
213-106-9
Product Categories:
  • GAMIBETAL
  • Pharmaceutical material and intermeidates
Mol File:
924-49-2.mol
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DL-GAMMA-AMINO-B-HYDROXYBUTYRIC ACIDCRYS TALLINE Chemical Properties

Melting point:
223 °C (dec.) (lit.)
Boiling point:
222.38°C (rough estimate)
Density 
1.3126 (rough estimate)
refractive index 
1.4183 (estimate)
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
solubility 
Water (Sparingly)
pka
pK1: 3.834(+1);pK2: 9.487(0) (25°C,μ=0.1)
form 
Powder
color 
White to Yellow
Water Solubility 
almost transparency
Merck 
14,444
Stability:
Hygroscopic
LogP
-1.730 (est)
EPA Substance Registry System
4-Amino-3-hydroxybutyric acid (924-49-2)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36
WGK Germany 
3
RTECS 
ES7015000
TSCA 
Yes
HS Code 
29224985
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DL-GAMMA-AMINO-B-HYDROXYBUTYRIC ACIDCRYS TALLINE Usage And Synthesis

Chemical Properties

White crystalline powder

Uses

antiepileptic

Uses

Reduces uptake of iodine by the thyroid glands in animals. Antispasmodic

Definition

ChEBI: Gamma-amino-beta-hydroxybutyric acid is a gamma-amino acid comprising 4-aminobutyric acid having a 2-hydroxy substituent. It is a gamma-amino acid and a 3-hydroxy monocarboxylic acid. It is functionally related to a butyric acid. It is a conjugate acid of a 4-amino-3-hydroxybutanoate. It is a tautomer of a gamma-amino-beta-hydroxybutyric acid zwitterion.

Purification Methods

Crystallise the acid from H2O or aqueous EtOH. Recrystallise it by dissolving it (CO2H), pK Est( 2) in H2O and adding MeOH or EtOH. It is not very soluble in CHCl3 or EtOAc. [Renaud & Seebach Synthesis 424 1986, Beilstein 4 IV 3187.]

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