142-28-9

  • Product Name:1,3-Dichloropropane
  • Molecular Formula:C3H6Cl2
  • Purity:99%
  • Molecular Weight:112.987
Inquiry

Product Details

pd_meltingpoint:-99 ºC

Appearance:clear colourless liquid

Purity:99%

China cas 142-28-9 manufacturer wholesale 1,3-Dichloropropane at affordable price

  • Molecular Formula:C3H6Cl2
  • Molecular Weight:112.987
  • Appearance/Colour:clear colourless liquid 
  • Vapor Pressure:18.3mmHg at 25°C 
  • Melting Point:-99 ºC 
  • Refractive Index:n20/D 1.448(lit.)  
  • Boiling Point:120.4 °C at 760 mmHg 
  • Flash Point:32.2 °C 
  • PSA:0.00000 
  • Density:1.188 g/cm3 
  • LogP:1.85410 

1,3-Dichloropropane(Cas 142-28-9) Usage

Preparation

1,3-Dichloropropane is obtained by the action of propylene glycol with hydrochloric acid.1,3-Dichloropropane synthesis: A process for the preparation of 1,3-dichloropropane by reacting bis(3-hydroxypropyl)ether with hydrogen chloride, optionally in the presence of tertiary basic nitrogen compounds or other tertiary aliphatic bases as catalysts, distilling off the 1,3-dichloropropane and the water of reaction and working up the two phases. Process for the preparation of 1,3-dichloropropane

Synthesis Reference(s)

The Journal of Organic Chemistry, 29, p. 194, 1964 DOI: 10.1021/jo01024a045

Air & Water Reactions

Highly flammable.

Reactivity Profile

Halogenated aliphatic compounds, such as 1,3-Dichloropropane, are moderately or very reactive. Reactivity generally decreases with increased degree of substitution of halogen for hydrogen atoms. Low molecular weight haloalkanes are highly flammable and can react with some metals to form dangerous products. Materials in this group are incompatible with strong oxidizing and reducing agents. Also, they are incompatible with many amines, nitrides, azo/diazo compounds, alkali metals, and epoxides.

Health Hazard

INHALATION: May cause some central nervous system depression. EYES: May cause some pain and irritation. SKIN: Mild irritation.

Safety Profile

Moderately toxic by ingestion. Mutation data reported. A very dangerous fire hazard when exposed to heat or flame. When heated to decomposition it emits highly toxic fumes of Cl and phosgene. See also CHLORINATED HYDROCARBONS, ALIPHATIC; and PROPYLENE DICHLORIDE.

Definition

ChEBI: 1,3-dichloropropane is a chloroalkane that is propane in which a hydrogen from each of the terminal methyl groups has been replaced by a chlorine. It has a role as an environmental contaminant and a nematicide. It is a chloroalkane and a chlorohydrocarbon.

General Description

1,3-dichloropropane is a colorless watery liquid with a sweet odor. Sinks in?water. Produces irritating vapor. (USCG, 1999)

InChI:InChI=1/C3H6Cl2/c4-2-1-3-5/h1-3H2

142-28-9 Relevant articles

-

Krenzel' et al.

, (1959)

-

KINETICS AND MECHANISM OF THE REDUCTION OF POLYCHLOROALKANES BY THREITHYLSILANE, CATALYZED BY BINUCLEAR MANGANESE AND RHENIUM CARBONYLS

Il'inskaya, L. V.,Kuz'mina, N. A.,Gasanov, R. G.,Chukovskaya, E. Ts.

, p. 2087 - 2090 (1987)

-

Laser-Initiated Chain Reactions of Chlorine with Propane and Cyclopropane in Amorphous Films at 77 K

Sedlacek, Arthur J.,Mansueto, Edward S.,Wight, Charles A.

, p. 6223 - 6229 (1987)

Free radical reactions of chlorine with ...

Conformational Selectivity in the Solid-State Photochlorination of Cyclopropane

Tague, Thomas J.,Wight, Charles A.

, p. 3266 - 3269 (1993)

The solid-state free-radical chain react...

-

Levaillant

, (1936)

-

Solvent pressure effects in free radical reactions. 2. Reconciliation of the gas and condensed phase chlorination of cyclopropane

Tanko, James M.,Suleman, N. Kamrudin

, p. 5162 - 5166 (1994)

The results reported herein demonstrate ...

-

Morgan,Burstall

, p. 1497,1500 (1930)

-

-

Mayo

, p. 5392,5394 (1954)

-

Preparation method of dichloroalkane

-

Paragraph 0019, (2021/02/10)

The invention discloses a preparation me...

Method and system for producing 1, 3-propylene glycol from 1, 3-dichloropropanol

-

Paragraph 0083; 0086-0087; 0090; 0093-0094; 0097; 0100-0101, (2021/03/13)

The invention discloses a method and a s...

Continuous method for preparation of dihalogenated alkane from diol compound

-

Paragraph 0044-0050, (2020/03/16)

The invention discloses a continuous met...

Hydrodehalogenation of alkyl halides catalyzed by a trichloroniobium complex with a redox active α-diimine ligand

Nishiyama, Haruka,Hosoya, Hiromu,Parker, Bernard F.,Arnold, John,Tsurugi, Hayato,Mashima, Kazushi

supporting information, p. 7247 - 7250 (2019/07/02)

A high-valent d0 niobium(v) complex, (α-...

142-28-9 Process route

bis(1-chloro-2-propyl) ether
108-60-1,52438-91-2

bis(1-chloro-2-propyl) ether

2,3-Dichloro-1-propanol
616-23-9

2,3-Dichloro-1-propanol

1,3-Dichloropropane
142-28-9

1,3-Dichloropropane

3-monochloro-1,2-propanediol
96-24-2

3-monochloro-1,2-propanediol

Conditions
Conditions Yield
With hydrogen; at 250 ℃;
bis(1-chloro-2-propyl) ether
108-60-1,52438-91-2

bis(1-chloro-2-propyl) ether

2,3-Dichloro-1-propanol
616-23-9

2,3-Dichloro-1-propanol

1,3-Dichloro-2-propanol
96-23-1

1,3-Dichloro-2-propanol

1,3-Dichloropropane
142-28-9

1,3-Dichloropropane

3-monochloro-1,2-propanediol
96-24-2

3-monochloro-1,2-propanediol

Conditions
Conditions Yield
With hydrogen; at 200 ℃; Reagent/catalyst; Temperature;

142-28-9 Upstream products

  • 503-30-0
    503-30-0

    trimethylene oxide

  • 632-02-0
    632-02-0

    3-chloropropyl p-toluenesulfonate

  • 60-29-7
    60-29-7

    diethyl ether

  • 50-00-0
    50-00-0

    formaldehyd

142-28-9 Downstream products

  • 100620-48-2
    100620-48-2

    1-tert-butyl-4-(3-chloropropoxy)benzene

  • 102756-13-8
    102756-13-8

    1,3-bis-(4-tert-butyl-phenoxy)-propane

  • 2117-07-9
    2117-07-9

    hexa-Si-phenyl-Si,Si'-propanediyl-bis-silane

  • 2591-14-2
    2591-14-2

    2-[(3-chloropropyl)sulfanyl]-1,3-benzothiazole

Relevant Products