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Details

Stereochemistry ACHIRAL
Molecular Formula C6H14O
Molecular Weight 102.1748
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 1-HEXANOL

SMILES

CCCCCCO

InChI

InChIKey=ZSIAUFGUXNUGDI-UHFFFAOYSA-N
InChI=1S/C6H14O/c1-2-3-4-5-6-7/h7H,2-6H2,1H3

HIDE SMILES / InChI
Molecular Formula C6H14O
Molecular Weight 102.1748
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

Unknown
139594
PubMed

PubMed

TitleDatePubMed
Fragrance volatiles of developing and senescing carnation flowers.
2001 Apr
Dense nonaqueous phase liquid tracer tests: experimental results.
2001 Dec
Modulation of intercalating properties of pyrido[1,2-e]purins via side-chain modifications: NMR and MD studies.
2001 Feb
Absence of direct antioxidant effects from volatile anesthetics in primary mixed neuronal-glial cultures.
2001 Feb
Direct separation of the stereoisomers of methoxytetrahydronaphthalene derivatives, new agonist and antagonist ligands for melatonin receptors, by liquid chromatography on cellulose chiral stationary phases.
2001 Jan 12
Straight-chain alcohols exhibit a cutoff in potency for the inhibition of recombinant glutamate receptor subunits.
2001 Jul
Structure-activity relationships for a large diverse set of natural, synthetic, and environmental estrogens.
2001 Mar
Melatonin receptor agents: synthesis, resolution by HPLC on polysaccharides chiral stationary phases, absolute configuration, and pharmacology of the enantiomers of (+/-)-N-[[2[(7-fluoro-1,2,3,4-tetrahydronaphthalen-1-yl)ethyl]acetamide.
2001 May 5
Helical ribbon aggregate composed of a crown-appended cholesterol derivative which acts as an amphiphilic gelator of organic solvents and as a template for chiral silica transcription.
2001 Sep 12
Screening of variables in beta-xylosidase recovery using cetyl trimethyl ammonium bromide reversed micelles.
2001 Spring
Influence of lipid fraction, emulsifier fraction, and mean particle diameter of oil-in-water emulsions on the release of 20 aroma compounds.
2002 Apr 10
Selective protein extraction from Chlorobium tepidum chlorosomes using detergents. Evidence that CsmA forms multimers and binds bacteriochlorophyll a.
2002 Dec 3
Effects of primary alcohols on airway smooth muscle.
2002 Feb
Biochemical and structural changes in RBCs stored with different plasticizers: the role of hexanol.
2002 Jul
Sensory evaluation of character impact components in an apple model mixture.
2002 Jul
Organic modifiers for the separation of organic acids and bases by liquid chromatography.
2002 Jul 26
Solvent triggering between conformational states in amphiphilic shape-persistent macrocycles.
2002 Jun 12
ALA and ALA hexyl ester in free and liposomal formulations for the photosensitisation of tumour organ cultures.
2002 Mar 4
Sonolysis of surfactants in aqueous solutions: an accumulation of solute in the interfacial region of the cavitation bubbles.
2002 Sep
Organic solvent tolerance of halophilic archaea.
2003 Aug
Influence of solvent on the growth of ZnO nanoparticles.
2003 Jul 15
[Isolation of myoinositol from solutions of enzymatic biotransformation].
2003 Jul-Aug
Modulation of MRP1-like efflux activity in human erythrocytes caused by membrane perturbing agents.
2003 Jul-Sep
Cutinase-AOT interactions in reverse micelles: the effect of 1-hexanol.
2003 Jun
Energization of Comamonas testosteroni ATCC 17454 for indicating toxic effects of chlorophenoxy herbicides.
2003 Oct
Identification of the several new radicals formed in the reaction mixture of oxidized linoleic acid with ferrous ions using HPLC-ESR and HPLC-ESR-MS.
2003 Sep
Identification and sensory evaluation of volatile compounds in oxidized porcine liver.
2004 Jan 28
Patents

Patents

03932410
1
03937742
1
04014887
1
04049647
1
04105790
1
04430425
1
05182283
7
05264587
1
05476875
3
JP1063344A
1
JP2003522130A
4
JP2004532328A
2
JP2005029495A
1
JP2005132809A
1
JP2005338849A
1
JP2006025643A
1
JP2006325902A
2
JP2007511575A
1
JP2008260819A
1
JP2008531810A
4
JP2009161686A
1
JP2009501198A
1
JP2011508668A
16
JP2011512848A
2
JP4484432B2
1
JP4709825B2
1
JP4800960B2
3
JP5301553B2
1
JPH01184371A
1
JPH02300118A
1
JPH03261702A
1
JPH04103699A
1
JPH05117467A
1
JPH06263915A
1
JPH07305013A
1
JPH07313067A
1
JPS55105680A
1
JPS5665803A
1
JPS57126428A
1
JPS58164663A
1
JPS5841723A
1
JPS60192708A
1
JPS6094124A
1
JPS6136295A
1
JPS6185401A
1
JPS6245677A
1
JPS63305189A
2
JPS6396156A
1
JPS6490151A
1
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:12:20 GMT 2023
Edited
by admin
on Fri Dec 15 15:12:20 GMT 2023
Record UNII
6CP2QER8GS
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
1-HEXANOL
HSDB   MI  
Systematic Name English
N-HEXYL ALCOHOL
Common Name English
PENTYLCARBINOL
Systematic Name English
CAPROYL ALCOHOL
Systematic Name English
1-HEXANOL [MI]
Common Name English
HEXYL ALCOHOL
FCC   FHFI   INCI  
INCI  
Official Name English
FEMA NO. 2567
Code English
AMYLCARBINOL
Systematic Name English
HEXYL ALCOHOL [FCC]
Common Name English
1-HEXANOL [HSDB]
Common Name English
N-HEXANOL
Common Name English
HEXYL ALCOHOL [FHFI]
Common Name English
HEXYL ALCOHOL [INCI]
Common Name English
NSC-9254
Code English
1-HYDROXYHEXANE
Systematic Name English
Classification Tree Code System Code
CFR 21 CFR 172.515
Created by admin on Fri Dec 15 15:12:20 GMT 2023 , Edited by admin on Fri Dec 15 15:12:20 GMT 2023
JECFA EVALUATION HEXYL ALCOHOL
Created by admin on Fri Dec 15 15:12:20 GMT 2023 , Edited by admin on Fri Dec 15 15:12:20 GMT 2023
EPA PESTICIDE CODE 79047
Created by admin on Fri Dec 15 15:12:20 GMT 2023 , Edited by admin on Fri Dec 15 15:12:20 GMT 2023
Code System Code Type Description
WIKIPEDIA
1-HEXANOL
Created by admin on Fri Dec 15 15:12:20 GMT 2023 , Edited by admin on Fri Dec 15 15:12:20 GMT 2023
PRIMARY
NSC
9254
Created by admin on Fri Dec 15 15:12:20 GMT 2023 , Edited by admin on Fri Dec 15 15:12:20 GMT 2023
PRIMARY
SMS_ID
100000144469
Created by admin on Fri Dec 15 15:12:20 GMT 2023 , Edited by admin on Fri Dec 15 15:12:20 GMT 2023
PRIMARY
CAS
111-27-3
Created by admin on Fri Dec 15 15:12:20 GMT 2023 , Edited by admin on Fri Dec 15 15:12:20 GMT 2023
PRIMARY
PUBCHEM
8103
Created by admin on Fri Dec 15 15:12:20 GMT 2023 , Edited by admin on Fri Dec 15 15:12:20 GMT 2023
PRIMARY
EPA CompTox
DTXSID8021931
Created by admin on Fri Dec 15 15:12:20 GMT 2023 , Edited by admin on Fri Dec 15 15:12:20 GMT 2023
PRIMARY
ECHA (EC/EINECS)
203-852-3
Created by admin on Fri Dec 15 15:12:20 GMT 2023 , Edited by admin on Fri Dec 15 15:12:20 GMT 2023
PRIMARY
EVMPD
SUB121012
Created by admin on Fri Dec 15 15:12:20 GMT 2023 , Edited by admin on Fri Dec 15 15:12:20 GMT 2023
PRIMARY
JECFA MONOGRAPH
8
Created by admin on Fri Dec 15 15:12:20 GMT 2023 , Edited by admin on Fri Dec 15 15:12:20 GMT 2023
PRIMARY
FDA UNII
6CP2QER8GS
Created by admin on Fri Dec 15 15:12:20 GMT 2023 , Edited by admin on Fri Dec 15 15:12:20 GMT 2023
PRIMARY
MESH
C036260
Created by admin on Fri Dec 15 15:12:20 GMT 2023 , Edited by admin on Fri Dec 15 15:12:20 GMT 2023
PRIMARY
CHEBI
87393
Created by admin on Fri Dec 15 15:12:20 GMT 2023 , Edited by admin on Fri Dec 15 15:12:20 GMT 2023
PRIMARY
MERCK INDEX
m6004
Created by admin on Fri Dec 15 15:12:20 GMT 2023 , Edited by admin on Fri Dec 15 15:12:20 GMT 2023
PRIMARY Merck Index
HSDB
565
Created by admin on Fri Dec 15 15:12:20 GMT 2023 , Edited by admin on Fri Dec 15 15:12:20 GMT 2023
PRIMARY
NIH
NCATS
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