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质量水平
方案
97%
表单
liquid
折射率
n20/D 1.4510 (lit.)
沸点
176-178 °C (lit.)
mp
-2 °C (lit.)
密度
0.943 g/mL at 25 °C (lit.)
SMILES字符串
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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Danger
危险声明
危险分类
Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 2 - Eye Dam. 1 - Skin Corr. 1B
储存分类代码
8A - Combustible corrosive hazardous materials
WGK
WGK 3
闪点(°F)
188.6 °F - closed cup
闪点(°C)
87 °C - closed cup
个人防护装备
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
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
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
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)
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
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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