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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
Structure of 2-METHYL-1-BUTANOL

SMILES

CCC(C)CO

InChI

InChIKey=QPRQEDXDYOZYLA-UHFFFAOYSA-N
InChI=1S/C5H12O/c1-3-5(2)4-6/h5-6H,3-4H2,1-2H3

HIDE SMILES / InChI
Molecular Formula C5H12O
Molecular Weight 88.1482
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Approval Year

Unknown
139594
PubMed

PubMed

TitleDatePubMed
Volatile metabolites from actinomycetes.
2002 Apr 24
One-pot sequences of reactions with sol-gel entrapped opposing reagents: an enzyme and metal-complex catalysts.
2002 Dec 4
Attractant volatiles released by female and male Triatoma infestans (Hemiptera: Reduviidae), a vector of chagas disease: chemical analysis and behavioral bioassay.
2002 Jan
Growth and aroma production by Staphylococcus xylosus, S. carnosus and S. equorum--a comparative study in model systems.
2002 May 5
Volatiles in a sausage surface model-influence of Penicillium nalgiovense, Pediococcus pentosaceus, ascorbate, nitrate and temperature.
2004 Feb
Growth and production of volatiles by Staphylococcus carnosus in dry sausages: Influence of inoculation level and ripening time.
2004 Jul
Dynamics of glass-forming liquids. VIII. Dielectric signature of probe rotation and bulk dynamics in branched alkanes.
2004 Nov 8
Higher-alcohols biorefinery: improvement of catalyst for ethanol conversion.
2004 Spring
Volatile metabolite production of spoilage micro-organisms on a mixed-lettuce agar during storage at 7 degrees C in air and low oxygen atmosphere.
2006 Nov 1
Potential of the volatile-producing fungus Muscodor albus for control of building molds.
2007 Mar
Using generic pheromone lures to expedite identification of aggregation pheromones for the cerambycid beetles Xylotrechus nauticus, Phymatodes lecontei, and Neoclytus modestus modestus.
2007 May
Carnobacterium: positive and negative effects in the environment and in foods.
2007 Sep
Filament formation in Saccharomyces cerevisiae--a review.
2008
Cultured skin microbiota attracts malaria mosquitoes.
2009 Dec 17
Profiling fruit volatiles in the progeny of a 'Royal Gala' x 'Granny Smith' apple (Malus x domestica) cross.
2009 Sep 9
Synthetic biology guides biofuel production.
2010
3-Methyl-1-butanol production in Escherichia coli: random mutagenesis and two-phase fermentation.
2010 Apr
Relationship between changes in the total concentration of acetic acid bacteria and major volatile compounds during the acetic acid fermentation of white wine.
2010 Dec
Evolution, genomic analysis, and reconstruction of isobutanol tolerance in Escherichia coli.
2010 Dec 21
Pentanol isomer synthesis in engineered microorganisms.
2010 Jan
Engineering the isobutanol biosynthetic pathway in Escherichia coli by comparison of three aldehyde reductase/alcohol dehydrogenase genes.
2010 Jan
Engineering Corynebacterium glutamicum for isobutanol production.
2010 Jul
Patents

Patents

08680095
2
Substance Class Chemical
Created
by admin
on Fri Dec 15 18:29:37 UTC 2023
Edited
by admin
on Fri Dec 15 18:29:37 UTC 2023
Record UNII
7VTJ239ASU
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
2-METHYL-1-BUTANOL
HSDB   MI  
Systematic Name English
SEC-BUTYLCARBINOL
Systematic Name English
(±)-2-METHYL-1-BUTANOL [FHFI]
Common Name English
ACTIVE AMYL ALCOHOL
Systematic Name English
PRIMARY ACTIVE AMYL ALCOHOL
Common Name English
2-METHYL-1-BUTANOL,(±)-
Common Name English
2-METHYL-N-BUTANOL
Common Name English
2-METHYLBUTYL ALCOHOL
Systematic Name English
2-METHYL-1-BUTANOL [HSDB]
Common Name English
ACTIVE PRIMARY AMYL ALCOHOL
Common Name English
FEMA NO. 3998
Code English
(±)-2-METHYL-1-BUTANOL
FHFI  
Systematic Name English
2-METHYL-1-BUTANOL [MI]
Common Name English
NSC-8431
Code English
Classification Tree Code System Code
JECFA EVALUATION (+/-)-2-METHYL-1-BUTANOL
Created by admin on Fri Dec 15 18:29:37 UTC 2023 , Edited by admin on Fri Dec 15 18:29:37 UTC 2023
EPA PESTICIDE CODE 431602
Created by admin on Fri Dec 15 18:29:37 UTC 2023 , Edited by admin on Fri Dec 15 18:29:37 UTC 2023
Code System Code Type Description
EPA CompTox
DTXSID5027069
Created by admin on Fri Dec 15 18:29:37 UTC 2023 , Edited by admin on Fri Dec 15 18:29:37 UTC 2023
PRIMARY
HSDB
5626
Created by admin on Fri Dec 15 18:29:37 UTC 2023 , Edited by admin on Fri Dec 15 18:29:37 UTC 2023
PRIMARY
FDA UNII
7VTJ239ASU
Created by admin on Fri Dec 15 18:29:37 UTC 2023 , Edited by admin on Fri Dec 15 18:29:37 UTC 2023
PRIMARY
NSC
8431
Created by admin on Fri Dec 15 18:29:37 UTC 2023 , Edited by admin on Fri Dec 15 18:29:37 UTC 2023
PRIMARY
JECFA MONOGRAPH
1208
Created by admin on Fri Dec 15 18:29:37 UTC 2023 , Edited by admin on Fri Dec 15 18:29:37 UTC 2023
PRIMARY
CAS
137-32-6
Created by admin on Fri Dec 15 18:29:37 UTC 2023 , Edited by admin on Fri Dec 15 18:29:37 UTC 2023
PRIMARY
MERCK INDEX
m7374
Created by admin on Fri Dec 15 18:29:37 UTC 2023 , Edited by admin on Fri Dec 15 18:29:37 UTC 2023
PRIMARY Merck Index
CHEBI
48945
Created by admin on Fri Dec 15 18:29:37 UTC 2023 , Edited by admin on Fri Dec 15 18:29:37 UTC 2023
PRIMARY
PUBCHEM
8723
Created by admin on Fri Dec 15 18:29:37 UTC 2023 , Edited by admin on Fri Dec 15 18:29:37 UTC 2023
PRIMARY
ECHA (EC/EINECS)
205-289-9
Created by admin on Fri Dec 15 18:29:37 UTC 2023 , Edited by admin on Fri Dec 15 18:29:37 UTC 2023
PRIMARY
WIKIPEDIA
2-METHYL-1-BUTANOL
Created by admin on Fri Dec 15 18:29:37 UTC 2023 , Edited by admin on Fri Dec 15 18:29:37 UTC 2023
PRIMARY
NIH
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