U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ACHIRAL
Molecular Formula C10H20O2
Molecular Weight 172.2646
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of OCTYL ACETATE

SMILES

CCCCCCCCOC(C)=O

InChI

InChIKey=YLYBTZIQSIBWLI-UHFFFAOYSA-N
InChI=1S/C10H20O2/c1-3-4-5-6-7-8-9-12-10(2)11/h3-9H2,1-2H3

HIDE SMILES / InChI

Molecular Formula C10H20O2
Molecular Weight 172.2646
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Odorant-binding proteins of the malaria mosquito Anopheles funestus sensu stricto.
2010-10-22
Characterization of volatile compounds of Daucus crinitus Desf. Headspace Solid Phase Microextraction as alternative technique to Hydrodistillation.
2010-09-21
Sample preparation based on matrix solid-phase dispersion and solid-phase extraction cleanup for the determination of organochlorine pesticides in fish.
2010-07-16
Structures, biological activities and phylogenetic relationships of terpenoids from marine ciliates of the genus Euplotes.
2010-07-08
Chemical composition and antibacterial activity of essential oil of Heracleum rechingeri Manden from Iran.
2010-07
Chemical composition, allelopatic and antimicrobial potentials of the essential oil of Zosima absinthifolia (Vent.) Link fruits from Iran.
2010-07
Membrane plasmalogen composition and cellular cholesterol regulation: a structure activity study.
2010-06-14
Relation between developmental stage, sensory properties, and volatile content of organically and conventionally grown pac choi (Brassica rapa var. Mei Qing Choi).
2010-05
Synthesis of hydrophilic and amphiphilic acryl sucrose monomers and their co-polymerisation with styrene, methylmethacrylate and α- and β-pinenes.
2010-04-16
DHP-derivative and low oxygen tension effectively induces human adipose stromal cell reprogramming.
2010-02-09
Antioxidant activities of some cameroonian plants extracts used in the treatment of intestinal and infectious diseases.
2010-01
Optogenetically Induced Olfactory Stimulation in Drosophila Larvae Reveals the Neuronal Basis of Odor-Aversion behavior.
2010
Simultaneous determination of cyclodol and diprazin by thin layer chromatography and high performance liquid chromatography.
2009-11
Isolation, characterization and antioxidative effect of phyllanthin against CCl4-induced toxicity in HepG2 cell line.
2009-10-30
The Mediterranean red alga Asparagopsis: a source of compounds against Leishmania.
2009-08-11
Anti-inflammatory and analgesic properties of Heracleum persicum essential oil and hydroalcoholic extract in animal models.
2009-07-30
Platensimycin activity against mycobacterial beta-ketoacyl-ACP synthases.
2009-07-17
Bioassay screening of the essential oil and various extracts from 4 spices medicinal plants.
2009-07
Development and validation of a sensitive and rapid non-aqueous LC-ESI-MS/MS method for measurement of diosgenin in the plasma of normal and hyperlipidemic rats: a comparative study.
2009-05-15
Identification of host attractants for the ethiopian fruit fly, Dacus ciliatus loew.
2009-05
A circuit supporting concentration-invariant odor perception in Drosophila.
2009
Ethyl 1-(4-chloro-phen-yl)-3-[1-(4-meth-oxy-phen-yl)-4-oxo-3-phenyl-azetidin-2-yl]-2-nitro-2,3,10,10a-tetra-hydro-1H,5H-pyr-rolo[1,2-b]isoquinoline-10a-carboxyl-ate.
2008-09-30
5-Bromo-2,4,6-trimethyl-3-phenyl-sulfinyl-1-benzofuran.
2008-08-23
2-Methyl-3-phenyl-sulfonyl-5-propyl-1-benzofuran.
2008-08-16
3-Methyl-sulfinyl-2-phenyl-1-benzofuran.
2008-08-06
1-[(4,5-Dimethyl-cyclo-hexa-1,4-dien-1-yl)sulfon-yl]-4-methyl-benzene.
2008-08-06
3,4-O-(2,3-Dimethoxy-butane-2,3-di-yl)-S-(4-methyl-phen-yl)-1-thia-α-d-manno-pyran-oside.
2008-06-28
(3S,3aS,5aS,7S,8S,10aS,10bR)-7,8-Dihydr-oxy-3-isopropyl-5a,8-dimethyl-2,3,4,5,5a,6,7,8,10a,10b-deca-hydro-cyclo-hepta-[e]indene-3a(1H)-carboxylic acid.
2008-06-28
6-[(E)-3,7-Dimethyl-octa-2,6-dien-yl]-5,7-dihydr-oxy-8-(2-methyl-butano-yl)-4-phenyl-2H-chromen-2-one from Mesua kunstleri King (Kosterm).
2008-06-25
5-Isopropyl-2-methyl-3-phenyl-sulfonyl-1-benzofuran.
2008-06-13
Methyl 5a-acetoxy-methyl-3-isopropyl-8-methyl-1,2,3,3a,4,5,5a,6,7,10,10a,10b-dodeca-hydro-7,10-endo-epidioxy-cylohepta-[e]indene-3a-carboxyl-ate.
2008-06-07
2,4,6,7-Tetra-methyl-3-phenyl-sulfinyl-1-benzofuran.
2008-05-24
5-Iodo-7-methyl-3-methyl-sulfinyl-2-phenyl-1-benzofuran.
2008-05-21
5-Ethyl-2-methyl-3-phenyl-sulfonyl-1-benzofuran.
2008-05-07
7-Bromo-2-methyl-1-(phenyl-sulfon-yl)naphtho[2,1-b]furan.
2008-04-30
5-Iodo-2,7-dimethyl-3-phenyl-sulfonyl-1-benzofuran.
2008-04-30
2,5-Dimethyl-3-phenyl-sulfonyl-1-benzofuran.
2008-04-16
3-(4-Chloro-phenyl-sulfon-yl)-2-methyl-naphtho[1,2-b]furan.
2008-04-16
2,5,7-Trimethyl-3-phenyl-sulfonyl-1-benzofuran.
2008-04-02
5-Bromo-2-methyl-3-phenyl-sulfonyl-1-benzofuran.
2008-04-02
2-Methyl-1-(phenyl-sulfon-yl)naphtho[2,1-b]furan.
2008-03-20
(±)-N-[4-Acetyl-5-methyl-5-(4-methyl-cyclo-hex-3-en-yl)-4,5-dihydro-1,3,4-thia-diazol-2-yl]acetamide.
2008-02-20
Racemic 4-(4-tert-butyl-phen-yl)-2,6-dimethyl-cyclo-hex-3-enecarboxylic acid.
2008-02-06
N-(1-Acetyl-r-7,c-9-diphenyl-4,8-dithia-1,2-diaza-spiro-[5.4]dec-2-en-3-yl)acet-amide.
2008-01-23
5-Iodo-2,7-dimethyl-3-phenyl-sulfinyl-1-benzofuran.
2008-01-23
2-Methyl-3-(phenyl-sulfon-yl)naphtho[1,2-b]furan.
2008-01-16
5-Hydr-oxy-7-meth-oxy-4H-chromen-4-one.
2007-12-18
cis-3-Methyl-1-phenyl-8a,9,10,11,12,12a,12b-hexa-hydro-1H,3bH-pyrazolo[3,4:2',3']pyrano[4',5',6'-kl]xanthene.
2007-12-12
7-Bromo-3-ethyl-9-phenyl-2-tosyl-pyrrolo[3,4-b]quinoline.
2007-12-06
Multiresidue determination of pesticides in juice by solid-phase extraction and gas chromatography-mass spectrometry.
2005-05-15
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:54:02 GMT 2025
Edited
by admin
on Mon Mar 31 18:54:02 GMT 2025
Record UNII
X0FN2J413S
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
NSC-67348
Preferred Name English
OCTYL ACETATE
FCC   FHFI  
Systematic Name English
OCTYL ACETATE [FCC]
Common Name English
N-OCTYL ACETATE
Common Name English
FEMA NO. 2806
Code English
ACETIC ACID, OCTYL ESTER
Common Name English
OCTYL ACETATE [FHFI]
Common Name English
CAPRYLYL ACETATE
Systematic Name English
Classification Tree Code System Code
CFR 21 CFR 172.515
Created by admin on Mon Mar 31 18:54:02 GMT 2025 , Edited by admin on Mon Mar 31 18:54:02 GMT 2025
JECFA EVALUATION OCTYL ACETATE
Created by admin on Mon Mar 31 18:54:02 GMT 2025 , Edited by admin on Mon Mar 31 18:54:02 GMT 2025
Code System Code Type Description
RXCUI
2048711
Created by admin on Mon Mar 31 18:54:02 GMT 2025 , Edited by admin on Mon Mar 31 18:54:02 GMT 2025
PRIMARY
NSC
67348
Created by admin on Mon Mar 31 18:54:02 GMT 2025 , Edited by admin on Mon Mar 31 18:54:02 GMT 2025
PRIMARY
PUBCHEM
8164
Created by admin on Mon Mar 31 18:54:02 GMT 2025 , Edited by admin on Mon Mar 31 18:54:02 GMT 2025
PRIMARY
JECFA MONOGRAPH
250
Created by admin on Mon Mar 31 18:54:02 GMT 2025 , Edited by admin on Mon Mar 31 18:54:02 GMT 2025
PRIMARY
EVMPD
SUB179219
Created by admin on Mon Mar 31 18:54:02 GMT 2025 , Edited by admin on Mon Mar 31 18:54:02 GMT 2025
PRIMARY
EPA CompTox
DTXSID8044202
Created by admin on Mon Mar 31 18:54:02 GMT 2025 , Edited by admin on Mon Mar 31 18:54:02 GMT 2025
PRIMARY
SMS_ID
100000164613
Created by admin on Mon Mar 31 18:54:02 GMT 2025 , Edited by admin on Mon Mar 31 18:54:02 GMT 2025
PRIMARY
WIKIPEDIA
OCTYL ACETATE
Created by admin on Mon Mar 31 18:54:02 GMT 2025 , Edited by admin on Mon Mar 31 18:54:02 GMT 2025
PRIMARY
CAS
112-14-1
Created by admin on Mon Mar 31 18:54:02 GMT 2025 , Edited by admin on Mon Mar 31 18:54:02 GMT 2025
PRIMARY
ECHA (EC/EINECS)
203-939-6
Created by admin on Mon Mar 31 18:54:02 GMT 2025 , Edited by admin on Mon Mar 31 18:54:02 GMT 2025
PRIMARY
CHEBI
87495
Created by admin on Mon Mar 31 18:54:02 GMT 2025 , Edited by admin on Mon Mar 31 18:54:02 GMT 2025
PRIMARY
DAILYMED
X0FN2J413S
Created by admin on Mon Mar 31 18:54:02 GMT 2025 , Edited by admin on Mon Mar 31 18:54:02 GMT 2025
PRIMARY
FDA UNII
X0FN2J413S
Created by admin on Mon Mar 31 18:54:02 GMT 2025 , Edited by admin on Mon Mar 31 18:54:02 GMT 2025
PRIMARY