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A43804

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
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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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

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

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

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

Group 4: Flammable liquids + Type 3 petroleums + Hazardous rank III + Water insoluble liquid

fsl

A43804-5ML: + A43804-VAR: + A43804-BULK: + A43804-500ML: + A43804-100ML:

jan

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Certificates of Analysis (COA)

Lot/Batch Number
1377552
1396061
1377549
04515KH
1178064

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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
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