require_once( "../navigation.include" ); ?>
check_image( "../cid_images/cid_441.png" ); ?>
check_image( "../cid_thumbs/cid_440030.png" ); ?>
check_image( "../cid_thumbs/cid_94318.png" ); ?>
check_image( "../cid_thumbs/cid_92135.png" ); ?>
check_image( "../cid_thumbs/cid_4841246.png" ); ?>
check_image( "../cid_thumbs/cid_4172682.png" ); ?>
check_image( "../cid_thumbs/cid_3571656.png" ); ?>
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check_image( "../cid_thumbs/cid_10920440.png" ); ?>
check_image( "../cid_thumbs/cid_3647261.png" ); ?>
check_image( "../cid_thumbs/cid_2935517.png" ); ?>
check_image( "../cid_thumbs/cid_339320.png" ); ?>
check_image( "../cid_thumbs/cid_2802693.png" ); ?>
check_image( "../cid_thumbs/cid_3542929.png" ); ?>
check_image( "../cid_thumbs/cid_6098237.png" ); ?>
check_image( "../cid_thumbs/cid_4445035.png" ); ?>
check_image( "../cid_thumbs/cid_1720510.png" ); ?>
check_image( "../cid_thumbs/cid_4480019.png" ); ?>
check_image( "../cid_thumbs/cid_3545205.png" ); ?>
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[1. The d-stereoisomer is one of the ketone bodies and is formed in ketogenesis; it is an important fuel for extrahepatic tissues; as an acyl derivative it is also an intermediate in fatty acid biosynthesis. The l-isomer is found as a coenzyme A derivative in β oxidation of fatty acids.
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pre_formula( "InChI=1/C4H8O3/c1-3(5)2-4(6)7/h3,5H,2H2,1H3,(H,6,7)/f/h6H", "jqp061/441.html" ); ?>
Molecular Formula:
C4H8O3
InChI: InChI=1/C4H8O3/c1-3(5)2-4(6)7/h3,5H,2H2,1H3,(H,6,7)/f/h6H
InChIKey: InChIKey=WHBMMWSBFZVSSR-BRMMOCHJCA
SMILES: CC(O)CC(O)=O
CAS number 300-85-6
Names:
beta-Hydroxybutyric acid
beta-Hydroxy-n-butyric acid
Butanoic acid, 3-hydroxy-
Butyric acid, 3-hydroxy-
3-hydroxybutanoic acid
3-hydroxybutyric acid
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Registries:
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PubChem CID 441
Beilstein =773861
CAS 300-85-6 (from NIST)
ChEBI 20067
PubChem ID 10329218
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require_once( "../ads.include" ); ?>
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