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Molecule
ID:104162
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₁₀H₂₀O₂
Molecular Mass
172.2646
Exact Mass
172.14632988
Charge
0
InChI
InChI=1S/C10H20O2/c1-3-5-6-7-8-9-10(11)12-4-2/h3-9H2,1-2H3
InChIKey
YYZUSRORWSJGET-UHFFFAOYSA-N
Canonic Smiles
CCCCCCCC(=O)OCC
Isomeric Smiles
CCCCCCCC(=O)OCC
Calculated Properties
JChem
LogD (pH = 7.4)
3.20
LogD (pH = 5.5)
3.20
Log P
3.20
Rotatable Bonds
8
H Donor
0
H Acceptors
1
Lipinski's Rule of Five
true
Acid pKa
-7.03
Polar Surface Area
26.30
Polarizability
21.50
Molar Refractivity
49.79
LOG S
-3.05
Data Source
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Names and Identifiers
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Registration numbers
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Properties
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Related Proteins
No Data Available
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Molecular Spectra
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Molecule Details
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References
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Bioactivity
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Quote
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General Information
Calculated Properties
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RDKit
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JChem
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Academic Data
Names and Identifiers
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Synonyms
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IUPAC name
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IUPAC Traditional name
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Properties
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Safety Information
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Product Information
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Physical Property
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Pharmacology Properties
Related Proteins
Molecular Spectra
Molecule Details
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MP Biomedicals
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Sigma Aldrich
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ChEBI
References
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PubChem Literature
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From Data Sources
Bioactivity
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PubChem BioAssay
Data Source
Commercial Catalog
MP Biomedicals
02154927
Sigma Aldrich
W244902
W244910
112321
21670
Alfa Aesar
B23450
Academic Data
PubChem
7799
ChEBI
CHEBI:87426
Names and Identifiers
Synonyms
Ethyl octanoate
CAPRYLIC ACID ETHYL ESTER
Ethyl caprylate
亚羊脂酸乙酯
Ethyl octanoate
辛酸乙酯
Octanoic acid ethyl ester
ethyl n-octanoate
ethyl octanoate
ethyl caprylate
caprylic acid ethyl ester
IUPAC name
ethyl octanoate
IUPAC Traditional name
ethyl octanoate
Registration numbers
CAS Number
106-32-1
EC Number
203-385-5
Beilstein Number
1754470
Flavis Number
9.111
MDL Number
MFCD00009552
Council of Europe Number
392c
392
FEMA ID
2449
PubChem SID
24901096
24847087
162091580
24901095
24852974
252237803
PubChem CID
7799
Merck Index
143778
Reaxys Registry
1754470
PubMed Citation Links
20096565
26213084
ACToR Database
106-32-1
CHEMBL
CHEMBL4633100
BRENDA Database
3.1.1.1
3.1.1.73
3.1.1.74
MetaboLights Database
MTBLS2330
MTBLS2096
MTBLS1391
MTBLS3840
MTBLS212
KEGG ID
C12292
BKMS React Database
67072
119100
BRENDA Ligand Database
119100
67072
HMDB Database
HMDB0040195
CHEBI ID
CHEBI:31574
CHEBI:87426
CompTox Database
DTXSID8051542
LIPID MAPS Instance
LMFA07010447
KNApSAcK Database
C00035613
SureChEMBL Database
SCHEMBL454
Molecule Details
MP Biomedicals
02154927
(Ethyl caprylate; Ethyl octanoate) Purity: 99.5% 1 ml = approx. 0.87 g
Sigma Aldrich
W244902
Packaging
1 kg in glass bottle
1 sample in glass bottle
4, 8, 9, 20 kg in poly drum
W244910
Packaging
1 kg in poly bottle
1 sample in glass bottle
100 g in poly bottle
4 kg in poly drum
112321
Packaging
5, 100, 500 g in glass bottle
Legal Information
ReagentPlus is a registered trademark of Sigma-Aldrich Co. LLC
Selectophore is a trademark of Sigma-Aldrich GmbH
ChEBI
CHEBI:87426
A fatty acid ethyl ester resulting from the formal condensation of octanoic acid with ethanol.
References
PubChem Literature
No Data Available
Click here to submit data
Bioactivity
PubChem BioAssay
Registration numbers
•
CAS Number
•
EC Number
•
Beilstein Number
•
Flavis Number
•
MDL Number
•
Council of Europe Number
•
FEMA ID
•
PubChem SID
•
PubChem CID
•
Merck Index
•
Reaxys Registry
•
PubMed Citation Links
•
ACToR Database
•
CHEMBL
•
BRENDA Database
•
MetaboLights Database
•
KEGG ID
•
BKMS React Database
•
BRENDA Ligand Database
•
HMDB Database
•
CHEBI ID
•
CompTox Database
•
LIPID MAPS Instance
•
KNApSAcK Database
•
SureChEMBL Database
Properties
Safety Information
MSDS Link
Download link
Source
Download link
Source
Download link
Source
Download link
Source
Download link
Source
RH0680000
Source
0°C
Source
FDA 21 CFR (172.515)
Source
EU Regulation 1334/2008 & 178/2002
Source
FCC
Source
2
Source
Warning
Source
Eyeshields, full-face respirator (US), Gloves, multi-purpose combination respirator cartridge (US), type ABEK (EN14387) respirator filter
Source
H315
Source
H227
Source
Irritant (Xi)
38
Source
Acute toxicity (oral, dermal, inhalation), category 4
Skin irritation, category 2
Eye irritation, category 2
Skin sensitisation, category 1
Specific Target Organ Toxicity – Single exposure, category 3
26
-
36
Source
是
Source
Product Information
99.5%
Source
≥98%
Source
≥99%
Source
≥98.0% (GC)
Source
99%
Source
Download link
Source
FG
Physical Property
0.87 g/ml
Source
0.867 g/mL at 20 °C(lit.)
Source
0.872
Source
206-208 °C(lit.)
Source
206-208°C
Source
75 °C
Source
167 °F
Source
Pharmacology Properties
no known allergens
Source
Source
Source
Source
natural
Source
Kosher
Source
NI
Source
Halal
Source
ReagentPlus®
Source
purum
Source
CH3(CH2)6COOC2H5
Source
178 °F
Source
81 °C
Source
79°C(174°F)
Source
0.02 mmHg ( 25 °C)
Source
n20/D 1.417(lit.)
Source
n20/D 1.418
Source
1.4170
Source
-48--47 °C(lit.)
Source
-47°C
Source
banana; floral; pear; pineapple; wine-like
Source
apricot; floral; pear; pineapple
Source
RTECS
Storage Condition
Regulation Compliance
German water hazard class
GHS Signal Word
Personal Protective Equipment
GHS Hazard statements
European Hazard Symbols
Risk Statements
GHS Pictograms
Safety Statements
TSCA Listed
Purity
Certificate of Analysis
Grade
Density
Boiling Point
Flash Point
Allergens
Linear Formula
Vapor Pressure
Refractive Index
Melting Point
Organoleptic