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210269

Sigma-Aldrich

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:
28954-12-3
Molecular Weight:
119.12
Beilstein:
1721645
EC Number:
249-327-2
MDL number:
MFCD00064268
UNSPSC Code:
12352200
eCl@ss:
32160406
PubChem Substance ID:
24852626
NACRES:
NA.22

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

SMILES string

C[C@H](O)[C@H](N)C(O)=O

InChI

1S/C4H9NO3/c1-2(6)3(5)4(7)8/h2-3,6H,5H2,1H3,(H,7,8)/t2-,3-/m0/s1

InChI key

AYFVYJQAPQTCCC-HRFVKAFMSA-N

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Storage Class Code

11 - Combustible Solids

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
0000031524
0000017147
BGBC0363V
BGBB8630
17429KB

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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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