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Molecule
ID:134791
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₄H₇NO₄
Molecular Mass
135.08798968
Exact Mass
135.04421739
Charge
0
InChI
InChI=1S/C4H7NO4/c5-2(4(8)9)1-3(6)7/h2H,1,5H2,(H,6,7)(H,8,9)/t2-/m0/s1/i2+1,4+1
InChIKey
CKLJMWTZIZZHCS-CJQZVISGSA-N
Canonic Smiles
OC(=O)C[13C@@H]([13C](=O)O)N
Isomeric Smiles
C([13C@@H]([13C](=O)O)N)C(=O)O
Calculated Properties
JChem
Acid pKa
1.7025436
H Acceptors
5
H Donor
3
LogD (pH = 5.5)
-4.018386
LogD (pH = 7.4)
-5.749634
Log P
-3.5037527
Molar Refractivity
26.5327
Polarizability
10.896484
Polar Surface Area
100.62
Rotatable Bonds
3
Lipinski's Rule of Five
true
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Related Proteins
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Molecule Details
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PubChem BioAssay
Data Source
Commercial Catalog
Sigma Aldrich
579793
Academic Data
PubChem
71308912
Names and Identifiers
Synonyms
L-天冬氨酸-1,2-13C2
L-Aspartic acid-1,2-13C2
IUPAC Traditional name
(2S)-2-amino(1,2-
1
3
C
2
)butanedioic acid
IUPAC name
(2S)-2-amino(1,2-
1
3
C
2
)butanedioic acid
Registration numbers
MDL Number
MFCD00190272
PubChem SID
162229067
PubChem CID
71308912
Molecule Details
Sigma Aldrich
579793
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
Safety Information
German water hazard class
3
Source
MSDS Link
Download link
Source
Personal Protective Equipment
Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
Source
Product Information
Linear Formula
HO2CCH213CH(NH2)13CO2H
Source
mol wt 135.07 by atom % calculation
Source
99 atom % 13C
Source
Physical Property
>300 °C (dec.)(lit.)
Source
M+2
Source
[α]25/D +25.0°, c = 2 in 5 M HCl
Source
Mol. Weight
Isotopic Purity
Melting Point
Mass Shift
Optical Rotation