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A43804

Sigma-Aldrich

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:
Molecular Weight:
89.14
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

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

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Signal Word

Danger

Hazard Statements

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 2 - Eye Dam. 1 - Skin Corr. 1B

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 3

Flash Point(F)

188.6 °F - closed cup

Flash Point(C)

87 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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
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)
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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