Details
Stereochemistry | RACEMIC |
Molecular Formula | C5H12O |
Molecular Weight | 88.1482 |
Optical Activity | ( + / - ) |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(C)C(C)O
InChI
InChIKey=MXLMTQWGSQIYOW-UHFFFAOYSA-N
InChI=1S/C5H12O/c1-4(2)5(3)6/h4-6H,1-3H3
Approval Year
PubMed
Title | Date | PubMed |
---|---|---|
Enantioseparation of chiral amino acids as the N(O,S)-ethoxycarbonylated diastereomeric esters by achiral dual-capillary column gas chromatography. | 2001 Dec |
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Enantioselectivity in Candida antarctica lipase B: a molecular dynamics study. | 2001 Feb |
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Rational design of enantioselective enzymes requires considerations of entropy. | 2001 Sep |
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Size as a parameter for solvent effects on Candida antarctica lipase B enantioselectivity. | 2002 Feb 11 |
|
Spectroscopic identification of amyl alcohol hydrates through free OH observation. | 2009 Aug 6 |
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Classification Tree | Code System | Code | ||
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JECFA EVALUATION |
3-METHYL-2-BUTANOL
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11732
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77517
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DTXSID20862268
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209-950-2
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598-75-4
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71162
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m7375
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3-METHYL-2-BUTANOL
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93FF0F303R
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SUBSTANCE RECORD