210269
L-allo-Threonine
99%
Synonym(s):
(2S,3S)-2-Amino-3-hydroxybutyric acid
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About This Item
Linear Formula:
CH3CH(OH)CH(NH2)CO2H
CAS Number:
Molecular Weight:
119.12
NACRES:
NA.22
PubChem Substance ID:
eCl@ss:
32160406
UNSPSC Code:
12352200
EC Number:
249-327-2
MDL number:
Beilstein/REAXYS Number:
1721645
InChI key
AYFVYJQAPQTCCC-HRFVKAFMSA-N
InChI
1S/C4H9NO3/c1-2(6)3(5)4(7)8/h2-3,6H,5H2,1H3,(H,7,8)/t2-,3-/m0/s1
SMILES string
C[C@H](O)[C@H](N)C(O)=O
assay
99%
form
powder
optical activity
[α]23/D +9.0°, c = 2 in H2O
reaction suitability
reaction type: solution phase peptide synthesis
color
white
mp
272 °C (dec.) (lit.)
application(s)
peptide synthesis
Storage Class
11 - Combustible Solids
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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E Meirzadeh et al.
Nature communications, 7, 13351-13351 (2016-11-09)
Doping is a primary tool for the modification of the properties of materials. Occlusion of guest molecules in crystals generally reduces their symmetry by the creation of polar domains, which engender polarization and pyroelectricity in the doped crystals. Here we
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