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Names | |||
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Preferred IUPAC name
3-Chloroprop-1-ene | |||
Other names | |||
Identifiers | |||
3D model (JSmol)
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ChEBI | |||
ChEMBL | |||
ChemSpider | |||
ECHA InfoCard | 100.003.144 | ||
EC Number |
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KEGG | |||
PubChem CID
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RTECS number |
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UNII | |||
UN number | 1100 | ||
CompTox Dashboard (EPA)
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Properties | |||
C3H5Cl | |||
Molar mass | 76.52 g·mol−1 | ||
Appearance | Colorless, brown, yellow, or purple liquid[1] | ||
Odor | pungent, unpleasant[1] | ||
Density | 0.94 g/mL | ||
Melting point | −135 °C (−211 °F; 138 K) | ||
Boiling point | 45 °C (113 °F; 318 K) | ||
0.36 g/100 ml (20 °C) | |||
Solubility | soluble in ether, acetone, benzene, chloroform | ||
Vapor pressure | 295 mmHg[1] | ||
Refractive index (nD)
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1.4055 | ||
Viscosity | 0.3130 mPa·s[2] | ||
Hazards | |||
GHS labelling: | |||
Danger | |||
H225, H302, H312, H315, H319, H332, H335, H341, H351, H373, H400 | |||
P201, P202, P210, P233, P240, P241, P242, P243, P260, P261, P264, P270, P271, P273, P280, P281, P301+P312, P302+P352, P303+P361+P353, P304+P312, P304+P340, P305+P351+P338, P308+P313, P312, P314, P321, P322, P330, P332+P313, P337+P313, P362, P363, P370+P378, P391, P403+P233, P403+P235, P405, P501 | |||
NFPA 704 (fire diamond) | |||
Flash point | −32 °C (−26 °F; 241 K) | ||
390 °C (734 °F; 663 K) | |||
Explosive limits | 2.9–11.2% | ||
Lethal dose or concentration (LD, LC): | |||
LC50 (median concentration)
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11000 mg/m3 (rat, 2 hr) 11500 mg/m3 (mouse, 2 hr) 5800 mg/m3 (guinea pig, 2 hr) 22500 mg/m3 (rabbit, 2 hr) 10500 mg/m3 (cat, 2 hr)[3] | ||
NIOSH (US health exposure limits): | |||
PEL (Permissible)
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TWA 1 ppm (3 mg/m3)[1] | ||
REL (Recommended)
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TWA 1 ppm (3 mg/m3) ST 2 ppm (6 mg/m3)[1] | ||
IDLH (Immediate danger)
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250 ppm[1] | ||
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Allyl chloride is the organic compound with the formula CH2=CHCH2Cl. This colorless liquid is insoluble in water but soluble in common organic solvents. It is mainly converted to epichlorohydrin, used in the production of plastics. It is a chlorinated derivative of propylene. It is an alkylating agent, which makes it both useful and hazardous to handle.[4]
Ullmann
was invoked but never defined (see the help page).