348414
1-Butylimidazole
98%
Synonym(s):
1-Butyl-1H-imidazole, 1-n-Butylimidazole, N-(n-Butyl)imidazole, N-Butyl-1H-imidazole, N-Butylimidazole, N-Butylimidazolium
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About This Item
Empirical Formula (Hill Notation):
C7H12N2
CAS Number:
Molecular Weight:
124.18
UNSPSC Code:
12352005
NACRES:
NA.22
PubChem Substance ID:
EC Number:
224-335-9
Beilstein/REAXYS Number:
109499
MDL number:
Assay:
98%
Form:
liquid
Quality Level
assay
98%
form
liquid
refractive index
n20/D 1.480 (lit.)
bp
114-116 °C/12 mmHg (lit.)
density
0.945 g/mL at 25 °C (lit.)
SMILES string
CCCCn1ccnc1
InChI
1S/C7H12N2/c1-2-3-5-9-6-4-8-7-9/h4,6-7H,2-3,5H2,1H3
InChI key
MCMFEZDRQOJKMN-UHFFFAOYSA-N
General description
1-Butylimidazole acts as an N-coordinated ligand. 1-Butylimidazole is formed as intermediate during the synthesis of a cationic cyclodextrin, used in the chiral separation of amino acids and anionic pharmaceuticals by capillary electrophoresis. Influence of 1-butylimidazole as base on the synthesis of dissymmetric chlorohydrin ester has been reported.
Application
1-Butylimidazole may be used in the synthesis of a heterocyclic mesomeric betaine. It was used in the synthesis of 1-(1-butyl-3-imidazolio)propane-3-sulfonate (BIm3S).
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 2 Inhalation - Eye Dam. 1 - Skin Corr. 1B
Storage Class
6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
wgk
WGK 3
flash_point_f
293.0 °F
flash_point_c
145 °C
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
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Joseph M Keane et al.
Journal of the American Chemical Society, 126(21), 6806-6815 (2004-05-27)
A series of metal complexes was synthesized in which arenes were dihapto-coordinated to pi-basic metal fragments having the general form [TpM(pi-acid)(L)], where Tp = hydridotris(pyrazolyl)borate, M = rhenium, molybdenum, or tungsten, pi-acid = CO or NO(+), and L = 1-methylimidazole
Giulia Mastellone et al.
Molecules (Basel, Switzerland), 25(13) (2020-07-10)
This paper proposes a new sustainable and simple strategy for the micro-scale extraction of phenolic compounds from grapevine leaves with analytical purpose. The method is based on a microwave-assisted solid-liquid extraction approach (MA-SLE), using an aqueous solution of an ionic
Kunakorn Chumnum et al.
Polymers, 13(3) (2021-02-13)
The self-healing composites were prepared from the combination of bromobutyl rubber (BIIR) and natural rubber (NR) blends filled with carbon nanotubes (CNT) and carbon black (CB). To reach the optimized self-healing propagation, the BIIR was modified with ionic liquid (IL)