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Molecule
ID:135192
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/c6-1-2-3(7)4(8)5(9)10-2/h2-9H,1H2/t2-,3-,4-,5?/m1/s1/i5+1
InChIKey
HMFHBZSHGGEWLO-LZOXQHQWSA-N
Canonic Smiles
OC[C@H]1O[13CH]([C@@H]([C@@H]1O)O)O
Isomeric Smiles
C([C@@H]1[C@H]([C@H]([13CH](O1)O)O)O)O
Calculated Properties
JChem
Acid pKa
11.305696
H Acceptors
5
H Donor
4
LogD (pH = 5.5)
-2.3022048
LogD (pH = 7.4)
-2.3022583
Log P
-2.3022044
Molar Refractivity
29.9609
Polarizability
12.6405
Polar Surface Area
90.15
Rotatable Bonds
1
Lipinski's Rule of Five
true
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Bioactivity
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General Information
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PubChem CID
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Bioactivity
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PubChem BioAssay
Data Source
Commercial Catalog
Sigma Aldrich
605352
310832
Academic Data
PubChem
16211987
Names and Identifiers
IUPAC Traditional name
(3R,4R,5R)-5-(hydroxymethyl)(2-
1
3
C)oxolane-2,3,4-triol
Synonyms
D-Ribose-1-13C
D-核糖-1-13C
IUPAC name
(3R,4R,5R)-5-(hydroxymethyl)(2-
1
3
C)oxolane-2,3,4-triol
Registration numbers
MDL Number
MFCD00064325
CAS Number
70849-24-0
PubChem SID
24858819
24881908
162229467
PubChem CID
16211987
Molecule Details
Sigma Aldrich
605352
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
C5H10O5
Source
Isotopic Purity
99 atom % 13C
Source
Mol. Weight
mol wt 151.12 by atom % calculation
Source
Safety Information
MSDS Link
Download link
Source
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Source
3
Source
Physical Property
M+1
Source
[α]20/D -20, c = 4 in H2O
Source
[α]20/D -20°, c = 4 in H2O
Source
88-92 °C (dec.)(lit.)
Source
94 °C (dec.)(lit.)
Source
German water hazard class
Mass Shift
Optical Rotation
Melting Point