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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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Samuel Treviño et al.
Journal of biochemical and molecular toxicology, 29(12), 587-594 (2015-07-28)
Alkaline phosphatase (ALP) activity in the serum and liver from rats administered with cadmium (Cd) in drinking water was studied. After metal administration, Cd showed a time-dependent accumulation in the liver, meanwhile metallothionein had a maximum increase at 1 month
H J Vial et al.
Biochemical pharmacology, 33(17), 2761-2770 (1984-09-01)
A number of choline and ethanolamine analogs were evaluated as inhibitors of P. falciparum growth in vitro. 1-Aziridineethanol, DL-2-amino-1,3-propranediol and D- or L-2-amino-1-butanol were the most efficient inhibitors of parasite multiplication, with an IC50 of 50-80 microM, whereas numerous other
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)
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)
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
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