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1-chlorobutane

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EntityQ161608· pop 22· linked from 13 articles

1-chlorobutane

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1-Chlorobutane is an alkyl halide with the chemical formula . It is a colorless, flammable liquid. It is used as a solvent in some industries due to its ability to dissolve both polar and non-polar substances. It is an alkylating reagent, that is used in organic synthesis to add a butyl group to other molecules.

In the Vinony graph

Within Vinony's link graph, 1-chlorobutane is referenced by 13 other articles, and connects out to lithium, International Standard Book Number and mass density.

It is catalogued under topics including Chembox having GHS data, Chembox image size set and Chloroalkanes.

Its subject is documented across 21 Wikipedia language editions.

Chemical data

Formula
C4H9Cl
Molecular weight
92.57 g/mol
IUPAC name
1-chlorobutane
SMILES
CCCCCl
InChIKey
VFWCMGCRMGJXDK-UHFFFAOYSA-N
XLogP
2.6
Polar surface area
0 Ų
H-bond donors
0
H-bond acceptors
0
Formal charge
0

via PubChem

Drug data · ChEMBL

Molecule type
Small molecule

via ChEMBL · EBI

Wikidata facts

Mass
92.039
Show 7 more facts
ionization energy
10.67
chemical formula
C₄H₉Cl
canonical SMILES
CCCCCl
electric dipole moment
2.05
Commons category
1-Chlorobutane
melting point
-123.1
boiling point
78.6
Sources (2)

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Encyclopedic overview

2 sections
Contents
  • Preparation and reactions
  • References

1-Chlorobutane is an alkyl halide with the chemical formula . It is a colorless, flammable liquid. It is used as a solvent in some industries due to its ability to dissolve both polar and non-polar substances. It is an alkylating reagent, that is used in organic synthesis to add a butyl group to other molecules.

==Preparation and reactions== It can be prepared from 1-butanol by treatment with hydrogen chloride: C4H9OH + HCl → C4H9Cl + H2O It reacts with lithium metal to give n-butyllithium: 2 Li + → + LiCl 1-Chlorobutane reacts with sodium hydroxide via nucleophilic substitution to produce butanol: + NaOH → + NaCl ==References==

Excerpted from Wikipedia’s “1-chlorobutane” article, available under the CC BY-SA 4.0 licence.

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