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A43804

Sigma-Aldrich

2-Amino-1-butanol

97%

Synonym(s):

(RS)-2-Amino-1-butanol, (±)-2-Amino-1-butanol, 1-(Hydroxymethyl)propylamine, 1-Hydroxy-sec-butylamine, 2-Amino-1-butanol, 2-Amino-1-hydroxybutane, 2-Aminobutyl alcohol

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About This Item

Linear Formula:
C2H5CH(NH2)CH2OH
CAS Number:
96-20-8
Molecular Weight:
89.14
EC Number:
202-488-2
MDL number:
MFCD00008095
UNSPSC Code:
12352100
PubChem Substance ID:
24890854
NACRES:
NA.22

assay

97%

form

liquid

refractive index

n20/D 1.4510 (lit.)

bp

176-178 °C (lit.)

mp

-2 °C (lit.)

density

0.943 g/mL at 25 °C (lit.)

SMILES string

CCC(N)CO

InChI

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

InChI key

JCBPETKZIGVZRE-UHFFFAOYSA-N

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signalword

Danger

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 2 - Eye Dam. 1 - Skin Corr. 1B

Storage Class

8A - Combustible corrosive hazardous materials

wgk_germany

WGK 3

flash_point_f

188.6 °F - closed cup

flash_point_c

87 °C - closed cup

ppe

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

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Chiral 2-amino-1-butanol xanthone derivatives as potential antiarrhythmic and hypotensive agents.
T Librowski et al.
Acta poloniae pharmaceutica, 56(1), 87-90 (2000-01-15)
R Ragonese et al.
Journal of pharmaceutical and biomedical analysis, 27(6), 995-1007 (2002-02-12)
Box-Behnken experimental designs do not appear to be extensively used in optimisation of analytical methods using capillary electrophoresis (CE). This paper describes the use of the Box-Behnken experimental design to optimise the factors affecting the separation of ethambutol hydrochloride (EB)
M L Ancelin et al.
Analytical biochemistry, 199(2), 203-209 (1991-12-01)
A rapid, convenient, and efficient method is presented to measure phosphatidylcholine, phosphatidylethanolamine, and phosphatidylinositol biosynthesis from [3H]choline, [3H]ethanolamine, and [3H]inositol, respectively. After incubation of the cells in 96-multi-well dishes with the appropriate radioactive precursor, cells were lysed with water and
Determination of optical purity by high-performance liquid chromatography of compounds of pharmaceutical interest.
G Gamberini et al.
Il Farmaco; edizione pratica, 43(11), 357-363 (1988-11-01)
M L Ancelin et al.
FEBS letters, 202(2), 217-223 (1986-07-07)
In Plasmodium falciparum-infected erythrocyte homogenates, the specific activity of ethanolamine kinase (7.6 +/- 1.4 nmol phosphoethanolamine/10(7) infected cells per h) was higher than choline kinase specific activity (1.9 +/- 0.2 nmol phosphocholine/10(7) infected cells per h). The Km of choline
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