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Molecule
ID:102759
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₁₈H₃₈O
Molecular Mass
270.49372
Exact Mass
270.29226584
Charge
0
InChI
InChI=1S/C18H38O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19/h19H,2-18H2,1H3
InChIKey
GLDOVTGHNKAZLK-UHFFFAOYSA-N
Canonic Smiles
CCCCCCCCCCCCCCCCCCO
Isomeric Smiles
CCCCCCCCCCCCCCCCCCO
Calculated Properties
JChem
LogD (pH = 7.4)
7.03
LogD (pH = 5.5)
7.03
Log P
7.03
Rotatable Bonds
16
H Donor
1
H Acceptors
1
Lipinski's Rule of Five
false
Acid pKa
-1.99
Polar Surface Area
20.23
Polarizability
38.65
Molar Refractivity
86.55
LOG S
-7.60
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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General Information
Calculated Properties
•
RDKit
•
JChem
Data Source
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Commercial Catalog
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Academic Data
Names and Identifiers
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IUPAC Traditional name
•
Synonyms
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IUPAC name
Registration numbers
Properties
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Physical Property
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Product Information
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Safety Information
Related Proteins
Molecular Spectra
Molecule Details
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MP Biomedicals
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Wikipedia
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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
•
PubChem BioAssay
Data Source
Commercial Catalog
MP Biomedicals
05217056
02102959
Sigma Aldrich
S5751
258768
O709
74722
PHR1115
74723
74720
Bide Pharmatech
BD17593
Alfa Aesar
A12020
Academic Data
Wikipedia
Stearyl_alcohol
PubChem
8221
ChEBI
CHEBI:32154
Names and Identifiers
IUPAC Traditional name
stearyl alcohol
Synonyms
Octadecyl alcohol
n-OCTADECYL ALCOHOL TECHNICAL GRADE
STEARYL ALCOHOL
1-Octadecanol
1-十八醇
stearyl alcohol
1-Octadecanol
硬脂醇
十八烷醇
Stearyl Alcohol
n-Octadecyl alcohol
Octadecan-1-ol
octadecan-1-ol
1-hydroxyoctadecane
n-octadecyl alcohol
octadecan-1-ol
1-octadecanol
n-1-octadecanol
n-octadecanol
octadecanol
stearyl alcohol
Stearylalkohol
IUPAC name
octadecan-1-ol
Registration numbers
CAS Number
112-92-5
EC Number
204-017-6
Beilstein Number
1362907
MDL Number
MFCD00002823
PubChem CID
8221
Unique Ingredient Identifier
2KR89I4H1Y
Chemspider ID
7928
Wikipedia Title
Stearyl_alcohol
CHEMBL
24640
CHEMBL24640
CHEBI ID
32154
CHEBI:32154
PubChem SID
162090072
24898043
24855658
24886710
29214853
Merck Index
148805
BKMS React Database
13295
106750
183336
MetaboLights Database
MTBLS2279
MTBLS2224
MTBLS1196
MTBLS208
MTBLS739
MTBLS1918
MTBLS763
MTBLS802
MTBLS3038
MTBLS804
MTBLS1561
MTBLS1858
MTBLS2074
MTBLS298
MTBLS3657
MTBLS2021
Patent number
EP1813276
EP1557167
EP1616562
EP1867317
US2007248632
EP1647268
US2007259045
WO2007130364
EP1352647
US2007207089
EP1522233
EP1647269
EP1901064
US2007191321
US2007265239
EP1547576
WO2005061515
US2007237820
EP1719509
WO2005019396
US2003022936
US2007190015
WO2007089100
US2006135623
EP1695700
WO2007099434
WO2006050002
EP1889609
US2005037067
EP1525882
EP1798234
US2008274094
US2007224143
US2007253911
EP1532990
EP1602355
EP1941901
WO2007115840
US2008293816
US2007254039
US2007178156
US2007196284
EP1764104
EP1847268
EP0964029
EP1857809
US2007269389
WO2007110878
US2007196504
US2007258911
WO2007105229
WO2007126777
EP1889621
EP1752128
EP1566176
EP1707200
US2007218092
EP1891953
WO2005108383
US2006084154
EP1506782
EP1897545
EP1057822
EP1639997
US2004170658
EP1541144
US2007207099
US2007196483
US2007207988
WO2007097818
US2007264344
EP1757261
EP1552815
US2003021759
WO2007132972
WO2007085637
EP1985287
WO2007136151
US2007248560
EP0966974
EP1552817
EP1690544
EP1839643
IntEnz Database
EC 1.2.1.84
ACToR Database
68911-61-5
112-92-5
Golm Database
73e385b5-653b-4eb2-a6d9-75090ace0603
7bd1189c-d353-4d44-893a-95a3c4661f23
5ee91ece-6862-4026-b849-f63aa1e70fe5
d144fb1b-27b4-4e8a-be6f-7c6f6a75f67d
e5f5b432-bb2e-48e4-b108-f769e67099cd
SwissLipids Database Link
SLM:000000583
PubMed Citation Links
2241202
8373640
11722503
26673629
10884288
23173706
2666627
1583866
21137365
BRENDA Database
2.3.1.75
1.1.3.20
1.1.1.1
1.14.15.3
1.1.1.2
1.2.1.84
1.14.14.28
3.1.1.50
2.5.1.26
1.14.16.5
1.1.1.192
CompTox Database
DTXSID8026935
LIPID MAPS Instance
LMFA05000085
Rhea Database
RHEA:44120
RHEA:36319
RHEA:59464
RHEA:38235
RHEA:40699
BRENDA Ligand Database
13295
106750
183336
KNApSAcK Database
C00029422
HMDB Database
HMDB0002350
NMRShiftDB Database
10008939
SureChEMBL Database
SCHEMBL23810
MetaCyc Database
CPD-7873
SABIO-RK Database
6756
Reaxys Registry
1362907
KEGG DRUG Database
D01924
Molecule Details
MP Biomedicals
02102959
Purity: ~99%
Wikipedia
Stearyl_alcohol
Sigma Aldrich
258768
Packaging
100 g in poly bottle
5 g in glass bottle
Legal Information
ReagentPlus is a registered trademark of Sigma-Aldrich Co. LLC
O709
Packaging
1 kg in poly bottle
2 kg in poly drum
PHR1115
General description
This certified reference material (CRM) is produced and certified in accordance with ISO/IEC 17025 and ISO Guide 34.
Other Notes
Values of analytes vary lot to lot.
74723
General description
Visit our Sensor Applications portal to learn more.
Legal Information
Selectophore is a trademark of Sigma-Aldrich GmbH
ChEBI
CHEBI:32154
A long-chain primary fatty alcohol consisting of a hydroxy function at C-1 of an unbranched saturated chain of 18 carbon atoms.
References
PubChem Literature
No Data Available
Click here to submit data
Bioactivity
PubChem BioAssay
Registration numbers
•
CAS Number
•
EC Number
•
Beilstein Number
•
MDL Number
•
PubChem CID
•
Unique Ingredient Identifier
•
Chemspider ID
•
Wikipedia Title
•
CHEMBL
•
CHEBI ID
•
PubChem SID
•
Merck Index
•
BKMS React Database
•
MetaboLights Database
•
Patent number
•
IntEnz Database
•
ACToR Database
•
Golm Database
•
SwissLipids Database Link
•
PubMed Citation Links
•
BRENDA Database
•
CompTox Database
•
LIPID MAPS Instance
•
Rhea Database
•
BRENDA Ligand Database
•
KNApSAcK Database
•
HMDB Database
•
NMRShiftDB Database
•
SureChEMBL Database
•
MetaCyc Database
•
SABIO-RK Database
•
Reaxys Registry
•
KEGG DRUG Database
Properties
Physical Property
Boiling Point
340 - 360 °C at 1013 hPa
Source
340°C
Source
210 °C at 15 mmHg (~2.0 kPa)
Source
170-171 °C/2 mmHg
Source
210 °C/15 mmHg
Source
210°C/15mm
Source
Melting Point
57.4 - 57.7 °C
Source
57.4°C
Source
59.4-59.8 °C
Source
56-59 °C(lit.)
Source
56-59 °C
Source
57-58 °C
Source
58-61 °C
Source
56-60°C
Source
Auto Ignition Point
450°C
Source
842 °F
Source
Vapor Pressure
.00015 hPa at 20 °C
Source
<0.01 mmHg ( 38 °C)
Source
Density
.8124 g/cm
3
at 59 °C
Source
0.812 g/cm3
Source
0.812 g/mL at 25 °C(lit.)
Source
Flash Point
ca. 195 °C (open cup)
Source
185°C (365°F)
Source
195 °C
Source
383 °F
Source
>113 °C
Source
>235.4 °F
Source
174°C(345°F)
Source
Solubility
1.1 x 10
-3
mg/L in water
Source
methanol: soluble10 mg/mL, clear, colorless
Source
Apperance
White solid
Source
Vapor Density
9.3 (vs air)
Source
Product Information
Purity
~99%
Source
99%
Source
95%
Source
≥95.0% (GC)
Source
≥99.5%
Source
≥99.5% (GC)
Source
≥99.0% (GC)
Source
95+%
Source
97%
Source
Download link
Source
Download link
Source
TECHNICAL
Source
ReagentPlus®
Source
purum
Source
certified reference material
Source
Selectophore™
Source
puriss.
Source
CH3(CH2)17OH
Source
traceable to USP 1622000
Source
traceable to PhEur S1350000
Source
pkg of 1 g
Source
Safety Information
RTECS
RG2010000
Source
MSDS Link
Download link
Source
Download link
Source
Download link
Source
Download link
Source
Download link
Source
Download link
Source
Download link
Source
Download link
Source
Room Temperature (15-30°C)
Source
~8 %
Source
Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
Source
nwg
Source
2-8°C
Source
P312
Source
H303
Source
是
Source
Certificate of Analysis
Grade
Linear Formula
Pharmacopeia Traceability
Packaging
Storage Condition
Explode Limits
Personal Protective Equipment
German water hazard class
Storage Temperature
GHS Precautionary statements
GHS Hazard statements
TSCA Listed