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Molecule
ID:102790
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₄H₉NO₃
Molecular Mass
119.11916
Exact Mass
119.05824315
Charge
0
InChI
InChI=1S/C4H9NO3/c1-2(6)3(5)4(7)8/h2-3,6H,5H2,1H3,(H,7,8)/t2?,3-/m0/s1
InChIKey
AYFVYJQAPQTCCC-NFJMKROFSA-N
Canonic Smiles
CC([C@@H](C(=O)O)N)O
Isomeric Smiles
CC(O)[C@H](N)C(=O)O
Calculated Properties
JChem
Acid pKa
2.207432
H Acceptors
4
H Donor
3
LogD (pH = 5.5)
-3.4708102
LogD (pH = 7.4)
-3.4806278
Log P
-3.4709635
Molar Refractivity
26.4598
Polarizability
10.868561
Polar Surface Area
83.55
Rotatable Bonds
2
Lipinski's Rule of Five
true
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General Information
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MP Biomedicals
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From Data Sources
Bioactivity
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PubChem BioAssay
Data Source
Commercial Catalog
MP Biomedicals
02103053
02156906
02199542
02194753
Academic Data
PubChem
11768555
Names and Identifiers
IUPAC name
(2S)-2-amino-3-hydroxybutanoic acid
IUPAC Traditional name
(2S)-2-amino-3-hydroxybutanoic acid
Synonyms
L-allo-THREONINE
L-THREONINE
2-Amino-3-hydroxybutyric acid
L-THREONINE, U.S.P.
L-THREONINE ALLO FREE
Registration numbers
CAS Number
72-19-5
28954-12-3
EC Number
200-774-1
249-327-2
PubChem SID
162088277
PubChem CID
11768555
Molecule Details
MP Biomedicals
02103053
Purity: 99%
Crystalline
02199542
White powder.
02194753
Cell Culture Reagent
Purity: 99%
Crystalline
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay
Properties
Safety Information
MSDS Link
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Storage Condition
Room Temperature (15-30°C)
Source
RTECS
XO8590000
Source
BA4055000
Source
Product Information
Purity
99%
Source
Certificate of Analysis
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USP
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Physical Property
Melting Point
255-257°C
Source
Grade