473960
(S)-3-Amino-1,2-propanediol
98%
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About This Item
Linear Formula:
H2NCH2CH(OH)CH2OH
CAS Number:
Molecular Weight:
91.11
UNSPSC Code:
12352116
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
1719122
Assay:
98%
InChI
1S/C3H9NO2/c4-1-3(6)2-5/h3,5-6H,1-2,4H2/t3-/m0/s1
SMILES string
NC[C@H](O)CO
InChI key
KQIGMPWTAHJUMN-VKHMYHEASA-N
assay
98%
optical activity
[α]20/D −28±1°, c = 4 in 5 M HCl
impurities
<0.5 mol
refractive index
n20/D 1.483 (lit.)
bp
117-119 °C/0.4 mmHg (lit.)
density
1.175 g/mL at 25 °C (lit.)
functional group
amine, hydroxyl
Application
(S)-3-Amino-1,2-propanediol-borate system can be used for the enantioseparation of monosaccharides, derivatized with either 1-phenyl-3-methyl-5-pyrazolone (PMP) or 8-aminonaphthalene-1,3,6-trisulfonate (ANT) by chiral ligand-exchange capillary electrophoresis (CE).
signalword
Danger
hcodes
Hazard Classifications
Skin Corr. 1B
Storage Class
8A - Combustible corrosive hazardous materials
wgk
WGK 3
flash_point_f
235.4 °F - closed cup
flash_point_c
113 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
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Chiral resolution of monosaccharides as 1-phenyl-3-methyl-5-pyrazolone derivatives by ligand-exchange CE using borate anion as a central ion of the chiral selector.
Kodama S, et al.
Electrophoresis, 27(23), 4730-4734 (2006)
Simultaneous chiral resolution of monosaccharides as 8-aminonaphthalene-1, 3, 6-trisulfonate derivatives by ligand-exchange CE using borate as a central ion of the chiral selector.
Kodama S, et al.
Electrophoresis, 28(21), 3930-3933 (2007)
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