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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:
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.)

functional group

amine
hydroxyl

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

Signal Word

Danger

Hazard Statements

H302,H314

Hazard Classifications

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

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 1

Flash Point(F)

185.0 °F

Flash Point(C)

85 °C

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
MKCQ3395
MKCP1367
MKCK0602
SHBJ5889
SHBG5325V

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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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