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Molecule
ID:131455
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₁₆H₃₂O₆
Molecular Mass
320.42168
Exact Mass
320.21988874
Charge
0
InChI
InChI=1S/C16H32O6/c1-2-3-4-5-6-7-8-9-10-21-16-15(20)14(19)13(18)12(11-17)22-16/h12-20H,2-11H2,1H3
InChIKey
JDRSMPFHFNXQRB-UHFFFAOYSA-N
Canonic Smiles
CCCCCCCCCCOC1OC(CO)C(C(C1O)O)O
Isomeric Smiles
CCCCCCCCCCOC1C(C(C(C(O1)CO)O)O)O
Calculated Properties
JChem
Acid pKa
12.210987
H Acceptors
6
H Donor
4
LogD (pH = 5.5)
1.7018982
LogD (pH = 7.4)
1.7018915
Log P
1.7018983
Molar Refractivity
82.1542
Polarizability
33.394142
Polar Surface Area
99.38
Rotatable Bonds
11
Lipinski's Rule of Five
true
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Molecular Spectra
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Molecule Details
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General Information
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IUPAC name
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From Data Sources
Bioactivity
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Data Source
Commercial Catalog
Sigma Aldrich
D5419
Academic Data
PubChem
4523964
Names and Identifiers
IUPAC name
2-(decyloxy)-6-(hydroxymethyl)oxane-3,4,5-triol
IUPAC Traditional name
2-(decyloxy)-6-(hydroxymethyl)oxane-3,4,5-triol
Synonyms
n-Decyl α-D-glucopyranoside
Registration numbers
PubChem CID
4523964
PubChem SID
162225733
EC Number
249-846-4
CAS Number
29781-81-5
MDL Number
MFCD00133591
Properties
Safety Information
German water hazard class
3
Source
GHS Hazard statements
H315
-
H319
-
H335
Source
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Source
European Hazard Symbols
Irritant (Xi)
Source
Risk Statements
36/37/38
Source
Safety Statements
26
-
36
Source
GHS Signal Word
Warning
Source
Storage Temperature
-20°C
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 Precautionary statements
P261
-
P305+P351+P338
Source
Product Information
Purity
~98% (GC)
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References
PubChem Literature
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Bioactivity
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PubChem CID
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