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1,4-Dichlorobutane

  • Product Name: 1,4-Dichlorobutane
  • CAS: 110-56-5
  • Purity:
  • Appearance: Colorless mobile liquid

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Factory supply good quality 1,4-Dichlorobutane 110-56-5 with stock

  • Molecular Formula:C4H8Cl2
  • Molecular Weight:127.014
  • Appearance/Colour:Colorless mobile liquid 
  • Vapor Pressure:23.7mmHg at 25°C 
  • Melting Point:-38 °C 
  • Refractive Index:n20/D 1.454(lit.)  
  • Boiling Point:153.9 °C at 760 mmHg 
  • Flash Point:40.8 °C 
  • PSA:0.00000 
  • Density:1.16 g/cm3 
  • LogP:2.24420 

1,4-dichlorobutane(Cas 110-56-5) Usage

General Description

1,4-dichlorobutane, also known as 1,4-DCB, is a chemical compound with the formula C4H8Cl2. It is a colorless liquid with a sharp, pungent odor and is insoluble in water but soluble in organic solvents. 1,4-DCB is primarily used as an intermediate in the production of other chemicals, including pharmaceuticals and pesticides. It is also used as a solvent and as a reagent in organic synthesis. The compound is classified as a chlorinated hydrocarbon and is considered to be toxic to the environment, with potential harmful effects on aquatic organisms. It is important to handle and dispose of 1,4-dichlorobutane with care to minimize its impact on human health and the environment.

InChI:InChI=1/C4H8Cl2/c1-2-3-4(5)6/h4H,2-3H2,1H3

110-56-5 Relevant articles

Determination of the hydrogen-bond basicity of weak and multifunctional bases: The case of lindane (γ-hexachlorocyclohexane)

Ouvrard, Carole,Lucon, Maryvonne,Graton, Jerome,Berthelot, Michel,Laurence, Christian

, p. 56 - 64 (2004)

We made use of four methods for determin...

POLAR RADICALS XVIII. ON THE MECHANISM OF CHLORINATION BY N-CHLOROAMINES: INTERMOLECULAR AND INTRAMOLECULAR ABSTRACTION.

Tanner, Dennis D.,Arhart, Richard,Meintzer, Christian P.

, p. 4261 - 4278 (1985)

The photochlorinations of the n-butyl, n...

-

Gunstone,F.D.,Sykes,P.J.

, p. 3055 - 3058 (1962)

-

-

Dees,Setser

, p. 2240 (1971)

-

Fragmentation of alkoxychlorocarbenes in the gas phase

Blake, Michael E,Jones Jr., Maitland,Zheng, Fengmei,Moss, Robert A

, p. 3069 - 3071 (2002)

In contrast to photolysis or thermal dec...

-

Zhulin,Rubinshtein

, (1976)

-

Diels-Alder Reactions of Trichlorophosphaethene

Teunissen, Herman T.,Hollebeek, Jan,Nieuwenhuizen, Peter J.,Baar, Ben L. M. van,Kanter, Frans J. J. de,Bickelhaupt, Friedrich

, p. 7439 - 7444 (1995)

The Diels-Alder reactions of trichloroph...

-

Fried,Kleene

, p. 2691 (1941)

-

Solid-phase reactions of alkanedicarboxylic acids with the Pb(OAc) 4-NH4Cl system

Nikishin, Gennady I.,Sokova, Lyubov L.,Makhaev, Viktor D.,Kapustina, Nadezhda I.

, p. 264 - 265 (2003)

The title reactions of HOOC(CH2)nCOOH ac...

Ethers as Oxygen Donor and Carbon Source in Non-hydrolytic Sol–Gel: One-Pot, Atom-Economic Synthesis of Mesoporous TiO2–Carbon Nanocomposites

Escamilla-Pérez, Angel Manuel,Louvain, Nicolas,Boury, Bruno,Brun, Nicolas,Mutin, P. Hubert

, p. 4982 - 4990 (2018)

Mesoporous TiO2–carbon nanocomposites we...

Preparation method of dichloroalkane

-

Paragraph 0020, (2021/02/10)

The invention discloses a preparation me...

Continuous method for preparation of dihalogenated alkane from diol compound

-

Paragraph 0051-0054; 0069-0075, (2020/03/16)

The invention discloses a continuous met...

Quinoline derivatives and its preparation method and in the application of neural protection in

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Paragraph 0024-0027, (2019/02/19)

The invention discloses a quinoline deri...

1,4-dichlorobutane production technology

-

Paragraph 0026-0036, (2019/10/23)

The invention provides a 1,4-dichlorobut...

110-56-5 Process route

ethene
74-85-1

ethene

1,2-dichloro-ethane
107-06-2,52399-93-6

1,2-dichloro-ethane

1,2-dichlorobutane
616-21-7,130232-87-0,130232-88-1

1,2-dichlorobutane

1,2-dichlorohexane
2162-92-7

1,2-dichlorohexane

1,2-dichlorooctane
21948-46-9,72778-28-0

1,2-dichlorooctane

1,2-dichlorodecane
34619-32-4

1,2-dichlorodecane

ethylbenzene
100-41-4,27536-89-6

ethylbenzene

1,4-dichlorobutane
110-56-5

1,4-dichlorobutane

Conditions
Conditions Yield
With dibenzoyl peroxide; at 100 ℃; Product distribution; Mechanism;
n-Butyl chloride
109-69-3

n-Butyl chloride

1,1-dichlorobutane
541-33-3

1,1-dichlorobutane

1,3-dichlorobutane
1190-22-3

1,3-dichlorobutane

1,2-dichlorobutane
616-21-7,130232-87-0,130232-88-1

1,2-dichlorobutane

1,4-dichlorobutane
110-56-5

1,4-dichlorobutane

Conditions
Conditions Yield
With sulfuryl dichloride; zeolite NaX; for 2h; Heating; Irradiation;
6 % Chromat.
23 % Chromat.
46 % Chromat.
25 % Chromat.
With sulfuryl dichloride; zeolite NaX; for 2h; Product distribution; Heating; Irradiation;
6 % Chromat.
23 % Chromat.
46 % Chromat.
25 % Chromat.
With norborn-2-ene; N-chlorohexamethyldisilazane; trans-di-O-tert-butyl hyponitrite; at 44.9 ℃; for 1h; Product distribution; Mechanism; further reagent, time;
With chlorine; In tetrachloromethane; at 20 ℃; Product distribution; other solvents, other temperatures;
With phenylchloroiodonium chloride; In tetrachloromethane; at 30 ℃; Product distribution; Mechanism; Irradiation; relative rate const., the correlation analysis, subst. phenylchloroiodonium chloride as reagents;
With N-chloropiperidine; 2,2'-azobis(isobutyronitrile); In trifluoroacetic acid; at 30 ℃; Product distribution; Rate constant; Irradiation; relative rate constants, position selectivity, substrate selectivity;
With chlorine; In benzene; at -10.1 ℃; Product distribution; dependence of the selectivity of chlorination on the conc. of benzene;
With N-chloropiperidine; 2,2'-azobis(isobutyronitrile); In trifluoroacetic acid; at 30 ℃; for 3h; Product distribution; Rate constant; Irradiation; other objects - relative reactivities and relative rate constants for the various positions of chlorination;
With chlorine; In 1,2-dichloro-benzene; at -20 - 50 ℃; Product distribution; Mechanism; Ratio of products and rate constants; different concentrations of o-dichlorobenzene.;
With chlorine;
With sulfuryl dichloride; dibenzoyl peroxide;

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