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471496

Sigma-Aldrich

2-(Butylamino)ethanol

≥98%

Synonym(s):

N-Butyl-2-hydroxyethylamine, N-Butylethanolamine

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About This Item

Linear Formula:
CH3(CH2)3NHCH2CH2OH
CAS Number:
111-75-1
Molecular Weight:
117.19
Beilstein/REAXYS Number:
1732522
EC Number:
203-904-5
MDL number:
MFCD00020570
UNSPSC Code:
12352100
PubChem Substance ID:
24870738
NACRES:
NA.22

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
GHS05,GHS07

signalword

Danger

hcodes

H302,H314

Hazard Classifications

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

Storage Class

8A - Combustible corrosive hazardous materials

wgk_germany

WGK 1

flash_point_f

185.0 °F

flash_point_c

85 °C

ppe

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

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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