1,2-Dichloropropane

Last updated
1,2-Dichloropropane [1]
1,2-dichloropropane skeletal.png
Names
Preferred IUPAC name
1,2-Dichloropropane
Other names
Propylene dichloride, Propane, 1,2-dichloro-
Identifiers
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
ECHA InfoCard 100.001.048 OOjs UI icon edit-ltr-progressive.svg
EC Number
  • 201-152-2
KEGG
PubChem CID
RTECS number
  • TX9625000
UNII
UN number 1279
  • InChI=1S/C3H6Cl2/c1-3(5)2-4/h3H,2H2,1H3 Yes check.svgY
    Key: KNKRKFALVUDBJE-UHFFFAOYSA-N Yes check.svgY
  • InChI=1/C3H6Cl2/c1-3(5)2-4/h3H,2H2,1H3
    Key: KNKRKFALVUDBJE-UHFFFAOYAR
  • ClCC(Cl)C
Properties
C3H6Cl2
Molar mass 112.98 g·mol−1
AppearanceColorless liquid
Odor like chloroform
Density 1.156 g/cm3
Melting point −100 °C (−148 °F; 173 K)
Boiling point 95 to 96 °C (203 to 205 °F; 368 to 369 K)
0.26 g/100 mL (at 20 °C)
Vapor pressure 40 mmHg (20°C) [2]
Hazards
GHS labelling:
GHS-pictogram-exclam.svg GHS-pictogram-silhouette.svg
Danger
H225, H302, H332, H350
P201, P202, P210, P233, P240, P241, P242, P243, P261, P264, P270, P271, P280, P281, P301+P312, P303+P361+P353, P304+P312, P304+P340, P308+P313, P312, P330, P370+P378, P403+P235, P405, P501
NFPA 704 (fire diamond)
NFPA 704.svgHealth 2: Intense or continued but not chronic exposure could cause temporary incapacitation or possible residual injury. E.g. chloroformFlammability 3: Liquids and solids that can be ignited under almost all ambient temperature conditions. Flash point between 23 and 38 °C (73 and 100 °F). E.g. gasolineInstability 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g. liquid nitrogenSpecial hazards (white): no code
2
3
0
Flash point 16 °C (61 °F; 289 K)
557 °C (1,035 °F; 830 K)
Explosive limits 3.4%-14.5% [2]
Lethal dose or concentration (LD, LC):
860 mg/kg (mouse, oral)
1947 mg/kg (rat, oral)
2000 mg/kg (guinea pig, oral) [3]
2000 ppm (rat, 4 hr)
720 ppm (mouse, 10 hr)
2980 ppm (rat, 8 hr) [3]
NIOSH (US health exposure limits):
PEL (Permissible)
TWA 75 ppm (350 mg/m3) [2]
REL (Recommended)
Ca [2]
IDLH (Immediate danger)
Ca [400 ppm] [2]
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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1,2-Dichloropropane is an organic compound classified as a chlorocarbon. It is a colorless, flammable liquid with a sweet odor. it is obtained as a byproduct of the production of epichlorohydrin, which is produced on a large scale. [4]

Contents

Uses

1,2-Dichloropropane is an intermediate in the production of perchloroethylene and other chlorinated chemicals. [4] It was once used as a soil fumigant, chemical intermediate, as well as an industrial solvent and was found in paint strippers, varnishes, and furniture finish removers but some of these uses have been discontinued. [5]

Carcinogenity

Following several cases of bile duct cancer among Japanese printing firm employees, an investigation by the Japanese Ministry of Health, Labour and Welfare concluded in March 2013 that these cases were likely due to the use of cleaning agents containing 1,2-dichloropropane. Thus, there is reasonable evidence that 1,2-dichloropropane may be a carcinogen. [6] [7]

Data from animal studies show tumor growth in the liver and mammary glands. [8] Further animal studies involving inhalation toxicity data has caused the National Institute for Occupational Safety and Health to classify 1,2-dichloropropane as a carcinogen and IDLH. [9]

Related Research Articles

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1,2-Dibromoethane, also known as ethylene dibromide (EDB), is an organobromine compound with the chemical formula C
2
H
4
Br
2
. Although trace amounts occur naturally in the ocean, where it is probably formed by algae and kelp, substantial amounts are produced industrially. It is a dense colorless liquid with a faint, sweet odor, detectable at 10 ppm. It is a widely used and sometimes-controversial fumigant. The combustion of 1,2-dibromoethane produces hydrogen bromide gas that is significantly corrosive.

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2-Nitrotoluene or ortho-nitrotoluene is an organic compound with the formula CH3C6H4NO2. It is pale yellow liquid that crystallizes in two forms, called α (−9.27 °C) and β (−3.17 °C). It is mainly a precursor to o-toluidine, which is an intermediate in the production of various dyes.

References

  1. 1,2-Dichloropropane at Sigma-Aldrich
  2. 1 2 3 4 5 NIOSH Pocket Guide to Chemical Hazards. "#0534". National Institute for Occupational Safety and Health (NIOSH).
  3. 1 2 "Propylene dichloride". Immediately Dangerous to Life or Health Concentrations (IDLH). National Institute for Occupational Safety and Health (NIOSH).
  4. 1 2 Manfred Rossberg, Wilhelm Lendle, Gerhard Pfleiderer, Adolf Tögel, Eberhard-Ludwig Dreher, Ernst Langer, Heinz Rassaerts, Peter Kleinschmidt, Heinz Strack, Richard Cook, Uwe Beck, Karl-August Lipper, Theodore R. Torkelson, Eckhard Löser, Klaus K. Beutel, Trevor Mann "Chlorinated Hydrocarbons" in Ullmann's Encyclopedia of Industrial Chemistry 2006, Wiley-VCH, Weinheim. doi : 10.1002/14356007.a06_233.pub2.
  5. "ToxFAQs for 1,2-Dichloropropane" . Retrieved 2010-06-16.
  6. Report by the Japanese Ministry of Health, Labour and Welfare
  7. Article in the Yomiuri Shimbun
  8. CDC - NIOSH Pocket Guide to Chemical Hazards
  9. Documentation for Immediately Dangerous To Life or Health Concentrations (IDLHs)