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Sigma-Aldrich

2-(Butylamino)ethanol

≥98%

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Synonym(s):
N-Butyl-2-hydroxyethylamine, N-Butylethanolamine
Linear Formula:
CH3(CH2)3NHCH2CH2OH
CAS Number:
Molecular Weight:
117.19
Beilstein:
1732522
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

≥98%

refractive index

n20/D 1.444 (lit.)

bp

198-200 °C (lit.)

density

0.891 g/mL at 25 °C (lit.)

SMILES string

CCCCNCCO

InChI

1S/C6H15NO/c1-2-3-4-7-5-6-8/h7-8H,2-6H2,1H3

InChI key

LJDSTRZHPWMDPG-UHFFFAOYSA-N

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General description

2-(Butylamino)ethanol is a secondary amine having a -OH group.

Application

2-(Butylamino)ethanol (N-Butylethanolamine) may be employed for the synthesis of 4-alkylamino-2,5,6-trimethyl -7-(2,4,6-trimethylphenyl)pyrrolo[2,3-d]pyrimidines and N-butyl-N-(2-nitroxyethyl)nitramine (BuNENA).

Pictograms

CorrosionExclamation mark

Signal Word

Danger

Hazard Statements

Hazard Classifications

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

WGK

WGK 1

Flash Point(F)

185.0 °F

Flash Point(C)

85 °C

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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Sitzmann.
Sitzmann ME, et al.
Propellants, Explosives, Pyrotechnics, 31(2), 124-130 (2006)
Ling-Wei Hsin et al.
Bioorganic & medicinal chemistry, 10(1), 175-183 (2001-12-12)
A series of compounds related to N-butyl-N-ethyl[2,5,6-trimethyl-7-(2,4,6-trimethylphenyl)pyrrolo[2,3-d]pyrimidin-4-yl]amine (1, antalarmin) have been prepared and evaluated for their CRHR1 binding affinity as the initial step in the development of selective high affinity hydrophilic nonpeptide corticotropin-releasing hormone type 1 receptor (CRHR1) antagonists. Calculated
M Sandin et al.
Antimicrobial agents and chemotherapy, 34(3), 491-493 (1990-03-01)
The antimicrobial effects of diethanolamine, dimethylamino-methyl-propanol, and butylethanolamine are greatly enhanced at high pH. Their antimicrobial activities are closely correlated with their uncharged forms, indicating that diffusion through cell membrane(s) is rate limiting for the antimicrobial action. Since these compounds

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