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Merck
CN

473960

(S)-3-Amino-1,2-propanediol

98%

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About This Item

Linear Formula:
H2NCH2CH(OH)CH2OH
CAS Number:
61278-21-5
Molecular Weight:
91.11
UNSPSC Code:
12352116
NACRES:
NA.22
PubChem Substance ID:
24870946
MDL number:
MFCD00798260
Beilstein/REAXYS Number:
1719122

Key Documents

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Product Name

(S)-3-Amino-1,2-propanediol, 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

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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).

pictograms

Corrosion
GHS05

signalword

Danger

hcodes

H314

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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Certificates of Analysis (COA)

Lot/Batch Number
BCBT8795
BCBC8542V
BCBD0955V
BCBC8542
BCBC7496

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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)
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)

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