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Molecule
ID:102432
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₄H₈O₄
Molecular Mass
120.10392
Exact Mass
120.04225874
Charge
0
InChI
InChI=1S/C4H8O4/c5-1-3(7)4(8)2-6/h1,3-4,6-8H,2H2/t3-,4+/m0/s1
InChIKey
YTBSYETUWUMLBZ-IUYQGCFVSA-N
Canonic Smiles
OC[C@H]([C@H](C=O)O)O
Isomeric Smiles
O=C[C@H](O)[C@H](O)CO
Calculated Properties
JChem
Acid pKa
12.445905
H Acceptors
4
H Donor
3
LogD (pH = 5.5)
-2.3076906
LogD (pH = 7.4)
-2.3076947
Log P
-2.3076906
Molar Refractivity
25.4206
Polarizability
10.220809
Polar Surface Area
77.76
Rotatable Bonds
3
Lipinski's Rule of Five
true
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
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RDKit
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JChem
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IUPAC name
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IUPAC Traditional name
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Synonyms
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Product Information
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Physical Property
Related Proteins
Molecular Spectra
Molecule Details
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MP Biomedicals
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Wikipedia
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Sigma Aldrich
References
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PubChem Literature
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From Data Sources
Bioactivity
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PubChem BioAssay
Data Source
Commercial Catalog
MP Biomedicals
02101653
Sigma Aldrich
E7625
18934
Alfa Aesar
B21093
Academic Data
Wikipedia
Erythrose
PubChem
94176
Names and Identifiers
IUPAC name
(2R,3R)-2,3,4-trihydroxybutanal
IUPAC Traditional name
erythrose
Synonyms
D-(-)-ERYTHROSE
Erythrose
D-(-)-Erythrose
D-赤藓糖, 糖浆
D-Erythrose, syrup
Registration numbers
EC Number
209-505-2
CAS Number
583-50-6
PubChem CID
94176
PubChem SID
162089598
24894651
Wikipedia Title
Erythrose
Chemspider ID
84990
CHEBI ID
27904
Beilstein Number
1721698
MDL Number
MFCD00006970
Merck Index
143690
Molecule Details
MP Biomedicals
02101653
Purity: 60-80%
Light yellow syrup
Wikipedia
Erythrose
Sigma Aldrich
E7625
Application
D-(-)-Erythrose is the D enantiomer of the aldose aldehyde Erythrose. D-Erythrose is used to study the mechanisms of organic microspherule formation and Maillard reactions.
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay
Registration numbers
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EC Number
•
CAS Number
•
PubChem CID
•
PubChem SID
•
Wikipedia Title
•
Chemspider ID
•
CHEBI ID
•
Beilstein Number
•
MDL Number
•
Merck Index
Properties
Product Information
Certificate of Analysis
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Source
Purity
≥75% (TLC)
Source
ca 70% w/v, >75% dry wt. basis
Source
Impurities
~30% water
Source
Empirical Formula (Hill Notation)
C4H8O4
Source
Safety Information
MSDS Link
Download link
Source
Download link
Source
Storage Condition
Room Temperature (15-30°C)
Source
NFPA704
1
1
0
Source
2-8°C
Source
3
Source
Eyeshields, Gloves
Source
Hygroscopic
Source
否
Source
Physical Property
Apperance
Syrup
Source
light yellow syrup
Source
Solubility
Very soluble in water
Source
Optical Rotation
-33 (c=2 in water, 72H)
Source
Refractive Index
1.4980
Source
Storage Temperature
German water hazard class
Personal Protective Equipment
Storage Warning
TSCA Listed