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A43804

2-Amino-1-butanol

Name: 2-Amino-1-butanol
Brand: ALDRICH

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

NACRES:

NA.22

PubChem Substance ID:

24890854

UNSPSC Code:

12352100

EC Number:

202-488-2

MDL number:

MFCD00008095

Assay:

97%

Form:

liquid

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Properties

Quality Level

100

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

Description

pictograms

GHS05,GHS07,GHS09

signalword

Danger

hcodes

H302,H314,H410

pcodes

P273 - P280 - P301 + P312 - P303 + P361 + P353 - P304 + P340 + P310 - P305 + P351 + P338

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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An original method for rapid serial determination of phospholipid biosynthesis. Applications to mammalian lymphocytic cells and a lower eucaryote, Plasmodium falciparum.

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

Synthesis and in vitro antimycobacterial activity of compounds derived from (R)- and (S)-2-amino-1-butanol - The crucial role of the configuration.

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

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)

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