Basic information Safety Supplier Related

3-Hydroxyglutaric Acid

Basic information Safety Supplier Related

3-Hydroxyglutaric Acid Basic information

Product Name:
3-Hydroxyglutaric Acid
Synonyms:
  • 2,4-Dideoxypentaric Acid
  • 3-Hydroxyglutaric Acid
  • 3-Hydroxy-pentanedioic Acid
  • b-Hydroxyglutaric Aci
  • Pentanedioic acid,3-hydroxy-
  • 3-Hydroxyglutaric acid,Endogenous Metabolite,3 Hydroxyglutaric acid,inhibit,Inhibitor,3Hydroxyglutaric acid
CAS:
638-18-6
MF:
C5H8O5
MW:
148.11
Product Categories:
  • Aliphatics
Mol File:
638-18-6.mol
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3-Hydroxyglutaric Acid Chemical Properties

Melting point:
94-96°C
Boiling point:
365.0±32.0 °C(Predicted)
Density 
1.508±0.06 g/cm3(Predicted)
storage temp. 
-20°C Freezer
solubility 
Methanol (Slightly), Water (Slightly)
form 
Solid
pka
3.93±0.10(Predicted)
color 
White to Pale Orange
InChI
InChI=1S/C5H8O5/c6-3(1-4(7)8)2-5(9)10/h3,6H,1-2H2,(H,7,8)(H,9,10)
InChIKey
ZQHYXNSQOIDNTL-UHFFFAOYSA-N
SMILES
C(O)(=O)CC(O)CC(O)=O
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3-Hydroxyglutaric Acid Usage And Synthesis

Chemical Properties

Off-White to Light Pink Solid

Uses

3-Hydroxyglutaric Acid (cas# 638-18-6) is a compound useful in organic synthesis.

Definition

ChEBI: 3-hydroxyglutaric acid is a 3 hydroxy carboxylic acid that is glutaric acid which is substituted by a hydroxy group at position 3. It is a diagnostic marker for glutaric aciduria type I. It has a role as a human urinary metabolite and a human blood serum metabolite. It is a 3-hydroxy carboxylic acid and an alpha,omega-dicarboxylic acid. It is functionally related to a glutaric acid. It is a conjugate acid of a 3-hydroxyglutarate(2-).

Biological Activity

3-Hydroxyglutaric acid is a glutaric acid derivative which is the byproduct of glutaric acidemia type I. Glutaric aciduria type I (glutaryl-CoA dehydrogenase deficiency) is an inborn error of metabolism th at usually manifests in infancy by an acute encephalopathic crisis and often results in permanent motor handicap. Studies indicate th at 3-hydroxyglutaric acid can be used as biomarker for GCDH (glutaryl-CoA dehydrogenase) deficiency. It is believed th at the excretion of 3-hydroxyglutaric acid is increased during ketosis, which occurs during glutaryl-CoA dehydrogenase deficiency. Studies on striatal cultures show th at IGF-1 and FGF-2 (bFGF) reduces 3-hydroxyglutaric acid toxicity in striatal neurons.

IC 50

Human Endogenous Metabolite

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