1,3-Dichloropropene
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1,3-Dichloropropene
structure -
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CAS No:
542-75-6
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Formula:
C3H4Cl2
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Chemical Name:
1,3-Dichloropropene
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Synonyms:
1-Propene,1,3-dichloro-;Propene,1,3-dichloro-;1,3-Dichloro-1-propene;1,3-Dichloropropene;α,γ-Dichloropropylene;1,3-Dichloropropylene;γ-Chloroallyl chloride;Telone;1,3-D;1,3-Dichloro-2-propene;3-Chloropropenyl chloride;3-Chloroallyl chloride;Telone II;Telone II-B;DD 95;D-D 92;Telone 92;NSC 6202;Dorlane II;8022-76-2;68525-58-6
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CAS No:
Description
clear yellowish to brownish liquid 1,3-Dichloropropene is a colorless to strawcolored liquid. Sharp, sweet, irritating, chloroform-like odor.
Characteristics
0
1.7
1,3-dichloropropene appears as a clear colorless liquid. Flash point 95°F. Denser (at 10.2 lb / gal) than water and insoluble in water. Vapors are heavier than air. Used to make other chemicals and as soil fumigant.
1.220 g/cm3 @ Temp: 25 °C
<-50 °C
108 °C
78 °F
1.469-1.475
H2O: <0.01 g/100 mL at 16.5 ºC
2-8°C
E-isomer 3700 Pa, Z-isomer 3500 Pa at 25 °C
3.86
Oral-Rat LD50: 470 mg/kg; Oral-Mouse LD50: 640 mg/kg
In case of open flame, high temperature, oxidant is more flammable; combustion produces toxic chloride fumes; heat decomposes toxic phosgene
Explosive limits , vol% in air: 5.3-14.5
Pungent odor
Bitter
Safety Information
III
3
UN 1992 3/PG 3
3
10-20/21-25-36/37/38-43-50/53-65-24/25-20
36/37-45-60-61
UC8310000
T,N
Storehouse ventilated at low temperature and dry; stored separately from oxidant; should not be stored for a long time to prevent polymerization
Stable under normal conditions.
P210, P233, P240, P241, P242, P243, P261, P264, P270, P271, P272, P273, P280, P301+P310, P302+P352, P303+P361+P353, P304+P312, P304+P340, P305+P351+P338, P312, P321, P322, P330, P331, P332+P313, P333+P313, P337+P313, P361, P362, P363, P370+P378, P391, P403+P233, P403+P235, P405, P501
H226
1,3-Dichloropropene Use and Manufacturing
The preparation method is obtained by reacting propylene and chlorine gas at 500-550°C after separation. When propylene is chlorinated to prepare epichlorohydrin, side reactions produce 3-chloropropene, 1, 3-dichloropropene and 1, 2-dichloropropane, which can also be produced after separation. The reaction equation is shown in the figure: CH3CH=CH2+Cl2→CH2ClCH=CH2+HClCH2ClCH=CH2+Cl2→ClCH=CHCH2Cl
Used in the production of pesticides, herbicides, etc.
Computed Properties
Molecular Weight:110.97
XLogP3:1.7
Rotatable Bond Count:1
Exact Mass:109.9690055
Monoisotopic Mass:109.9690055
Heavy Atom Count:5
Complexity:31.9
Defined Bond Stereocenter Count:1
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes
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