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Molecule
ID:134851
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₃H₇NO₃
Molecular Mass
107.07788968
Exact Mass
107.04930277
Charge
0
InChI
InChI=1S/C3H7NO3/c4-2(1-5)3(6)7/h2,5H,1,4H2,(H,6,7)/t2-/m0/s1/i2+1,3+1
InChIKey
MTCFGRXMJLQNBG-PIJHRLDMSA-N
Canonic Smiles
OC[13C@@H]([13C](=O)O)N
Isomeric Smiles
C([13C@@H]([13C](=O)O)N)O
Calculated Properties
JChem
Acid pKa
2.03399
H Acceptors
4
H Donor
3
LogD (pH = 5.5)
-3.8875728
LogD (pH = 7.4)
-3.8992038
Log P
-3.8877351
Molar Refractivity
22.041
Polarizability
9.0643015
Polar Surface Area
83.55
Rotatable Bonds
2
Lipinski's Rule of Five
true
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Molecular Spectra
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General Information
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IUPAC name
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IUPAC Traditional name
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CAS Number
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MDL Number
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PubChem SID
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PubChem CID
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Data Source
Commercial Catalog
Sigma Aldrich
589608
Academic Data
PubChem
71308944
Names and Identifiers
IUPAC name
(2S)-2-amino-3-hydroxy(1,2-
1
3
C
2
)propanoic acid
IUPAC Traditional name
(2S)-2-amino-3-hydroxy(1,2-
1
3
C
2
)propanoic acid
Synonyms
L-Serine-1,2-13C2
L-丝氨酸-1,2-13C2
Registration numbers
CAS Number
150146-96-6
MDL Number
MFCD01075522
PubChem SID
162229127
PubChem CID
71308944
Molecule Details
Sigma Aldrich
589608
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
Physical Property
Melting Point
222 °C (dec.)(lit.)
Source
Optical Rotation
[α]25/D +14.6°, c = 2 in 1 M HCl
Source
Mass Shift
M+2
Source
Product Information
Linear Formula
HOCH213CH(NH2)13CO2H
Source
Mol. Weight
mol wt 107.06 by atom % calculation
Source
99 atom % 13C
Source
Safety Information
3
Source
Download link
Source
Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
Source
Isotopic Purity
German water hazard class
MSDS Link
Personal Protective Equipment