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Molecule
ID:136944
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₅H₁₀O₅
Molecular Mass
151.12255484
Exact Mass
151.05617826
Charge
0
InChI
InChI=1S/C5H10O5/c6-2-1-10-5(9)4(8)3(2)7/h2-9H,1H2/t2-,3+,4-,5?/m1/s1/i5+1
InChIKey
SRBFZHDQGSBBOR-KOPVYNEGSA-N
Canonic Smiles
O[C@@H]1CO[13CH]([C@@H]([C@H]1O)O)O
Isomeric Smiles
C1[C@H]([C@@H]([C@H]([13CH](O1)O)O)O)O
Calculated Properties
JChem
Acid pKa
11.310624
H Acceptors
5
H Donor
4
LogD (pH = 5.5)
-2.3022048
LogD (pH = 7.4)
-2.3022575
Log P
-2.3022044
Molar Refractivity
29.9609
Polarizability
12.6405
Polar Surface Area
90.15
Rotatable Bonds
0
Lipinski's Rule of Five
true
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Related Proteins
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Bioactivity
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Data Source
Commercial Catalog
Sigma Aldrich
331104
Academic Data
PubChem
9815229
Names and Identifiers
IUPAC name
(3R,4S,5R)-(2-
1
3
C)oxane-2,3,4,5-tetrol
Synonyms
D-木糖-1-13C
D-Xylose-1-13C
IUPAC Traditional name
(3R,4S,5R)-(2-
1
3
C)oxane-2,3,4,5-tetrol
Registration numbers
CAS Number
70849-21-7
PubChem SID
24859934
162231211
PubChem CID
9815229
Molecule Details
Sigma Aldrich
331104
Packaging
This product may be available from bulk stock and can be packaged on demand. For information on pricing, availability and packaging, please contact Stable Isotopes Customer Service.
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay
Properties
Product Information
Empirical Formula (Hill Notation)
13CC4H10O5
Source
Isotopic Purity
99 atom % 13C
Source
Mol. Weight
mol wt 151.12 by atom % calculation
Source
Safety Information
MSDS Link
Download link
Source
2
Source
Physical Property
M+1
Source
[α]20/D +15°, c = 1 in H2O
Source
152-154 °C(lit.)
Source
German water hazard class
Mass Shift
Optical Rotation
Melting Point