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About This Item
Linear Formula:
C2H5CH(NH2)CH2OH
CAS Number:
Molecular Weight:
89.14
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
202-488-2
MDL number:
Assay:
97%
Form:
liquid
InChI key
JCBPETKZIGVZRE-UHFFFAOYSA-N
InChI
1S/C4H11NO/c1-2-4(5)3-6/h4,6H,2-3,5H2,1H3
SMILES string
CCC(N)CO
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.)
Quality Level
Related Categories
signalword
Danger
hcodes
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
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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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)
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)
Blandine Alberge et al.
The Biochemical journal, 425(1), 149-158 (2009-10-23)
The proliferation of the malaria-causing parasite Plasmodium falciparum within the erythrocyte is concomitant with massive phosphatidylcholine and phosphatidylethanolamine biosynthesis. Based on pharmacological and genetic data, de novo biosynthesis pathways of both phospholipids appear to be essential for parasite survival. The
Georgi M Dobrikov et al.
European journal of medicinal chemistry, 48, 45-56 (2011-12-14)
The synthesis of 47 structurally diverse compounds incorporating the (R)-2-amino-1-butanol motif has been realized. Ten of these compounds were found to exhibit in vitro specific activity against Mycobacterium tuberculosis H37Rv in a MIC range of 0.65 μM-14.03 μM. Five of the most active
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
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