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Sigma-Aldrich

(R)-(−)-2-Amino-1-butanol

98%

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About This Item

Linear Formula:
C2H5CH(NH2)CH2OH
CAS Number:
5856-63-3
Molecular Weight:
89.14
Beilstein/REAXYS Number:
1718929
EC Number:
227-476-4
MDL number:
MFCD00064419
UNSPSC Code:
12352116
PubChem Substance ID:
24858559
NACRES:
NA.22

assay

98%

form

liquid

optical activity

[α]19/D −10°, neat

optical purity

ee: 96% (GLC)

refractive index

n20/D 1.452

bp

172-174 °C (lit.)

mp

−2 °C (lit.)

density

0.943 g/mL at 20 °C (lit.)

SMILES string

CC[C@@H](N)CO

InChI

1S/C4H11NO/c1-2-4(5)3-6/h4,6H,2-3,5H2,1H3/t4-/m1/s1

InChI key

JCBPETKZIGVZRE-SCSAIBSYSA-N

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pictograms

Corrosion
GHS05

signalword

Danger

hcodes

H314

Hazard Classifications

Skin Corr. 1B

Storage Class

8A - Combustible corrosive hazardous materials

wgk_germany

WGK 3

ppe

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

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Datong Wu et al.
The Analyst, 145(9), 3395-3400 (2020-04-03)
Here, ionized chiral carbon dots, (S,S)-C-dots-1 (λex = 430 nm, λem = 480 nm), were synthesized via a facile route with relatively high quantum yield (∼24.4%) and used as a fluorescent chiral sensor. One of the advantages of the synthetic
Rym Hassani et al.
Chemico-biological interactions, 217, 41-48 (2014-04-15)
This paper describes the synthesis of new enantiomerically pure 2-cyanoethyl-oxazolines in one step starting from a wide range of amino alcohols and 4-ethoxy-4-iminobutanenitrile with high to good yields (73-96%) via an appropriate procedure which can be used for a selective

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