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Molecule
ID:5554
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₁₄H₂₈O₆
Molecular Mass
292.36852
Exact Mass
292.18858862
Charge
0
InChI
InChI=1S/C14H28O6/c1-2-3-4-5-6-7-8-19-14-13(18)12(17)11(16)10(9-15)20-14/h10-18H,2-9H2,1H3/t10-,11+,12+,13-,14-/m1/s1
InChIKey
HEGSGKPQLMEBJL-MBJXGIAVSA-N
Canonic Smiles
CCCCCCCCO[C@@H]1O[C@H](CO)[C@@H]([C@@H]([C@H]1O)O)O
Isomeric Smiles
CCCCCCCCO[C@@H]1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O
Calculated Properties
JChem
Acid pKa
12.210987
H Acceptors
6
H Donor
4
LogD (pH = 5.5)
0.8127609
LogD (pH = 7.4)
0.8127543
Log P
0.81276095
Molar Refractivity
72.9522
Polarizability
29.735554
Polar Surface Area
99.38
Rotatable Bonds
9
Lipinski's Rule of Five
true
ALOGPS 2.1
Log P
1.13
LOG S
-1.26
Solubility (Water)
1.60e+01 g/l
Data Source
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Related Proteins
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Molecular Spectra
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General Information
Calculated Properties
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RDKit
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JChem
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ALOGPS 2.1
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Names and Identifiers
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Synonyms
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IUPAC name
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IUPAC Traditional name
Registration numbers
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CAS Number
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MDL Number
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PubChem SID
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PubChem CID
Properties
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Safety Information
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Product Information
Related Proteins
Molecular Spectra
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From Data Sources
Bioactivity
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PubChem BioAssay
Data Source
Commercial Catalog
Sigma Aldrich
O0261
Academic Data
PubChem
9549264
DrugBank
DB07924
Names and Identifiers
Synonyms
octyl beta-D-galactopyranoside
Octyl β-D-galactopyranoside
IUPAC name
(2R,3R,4S,5R,6R)-2-(hydroxymethyl)-6-(octyloxy)oxane-3,4,5-triol
IUPAC Traditional name
β-D-galactopyranoside, octyl
Registration numbers
CAS Number
40427-75-6
MDL Number
MFCD00274445
PubChem SID
160968982
99444395
PubChem CID
9549264
Properties
Safety Information
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Source
GHS Pictograms
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
Source
GHS Hazard statements
H315
-
H319
-
H335
Source
GHS Precautionary statements
P261
-
P305+P351+P338
Source
Safety Statements
26
-
36
Source
GHS Signal Word
Warning
Source
European Hazard Symbols
Irritant (Xi)
Source
Risk Statements
36/37/38
Source
German water hazard class
3
Source
Storage Temperature
-20°C
Source
Product Information
Description
non-ionic
Source
Purity
≥98% (GC)
Source
Molecule Details
DrugBank
DB07924
Drug information: experimental
References
PubChem Literature
No Data Available
Click here to submit data
Bioactivity
PubChem BioAssay