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蒸汽密度
3.89 (vs air)
蒸汽压
40 mmHg ( 19.4 °C)
方案
99%
表单
liquid
自燃温度
1035 °F
expl. lim.
14.5 %
折射率
n20/D 1.439 (lit.)
沸点
95-96 °C (lit.)
mp
−100 °C (lit.)
密度
1.156 g/mL at 25 °C (lit.)
SMILES字符串
CC(Cl)CCl
InChI
1S/C3H6Cl2/c1-3(5)2-4/h3H,2H2,1H3
InChI key
KNKRKFALVUDBJE-UHFFFAOYSA-N
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警示用语：
Danger
危险分类
Acute Tox. 3 Inhalation - Acute Tox. 4 Oral - Carc. 1B - Flam. Liq. 2
储存分类代码
3 - Flammable liquids
WGK
WGK 3
闪点(°F)
59.0 °F - closed cup
闪点(°C)
15.0 °C - closed cup
个人防护装备
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
法规信息
新产品
Marcin Bartkowiak et al.
Journal of hazardous materials, 106(2-3), 107-114 (2004-06-05)
The ammonolysis of waste 1,2-dichloropropane (DCP) using liquid ammonia has been investigated. The influence of temperature, molar ratio of NH3/1,2-dichloropropane and reaction time was examined. The highest yield of the synthesis was achieved at a temperature of 140 degrees C
A J Tesoriero et al.
Environmental science & technology, 35(3), 455-461 (2001-05-16)
A shallow aquifer with different redox zones overlain by intensive agricultural activity was monitored for the occurrence of 1,2-dichloropropane (DCP) to assess the fate and origin of this pollutant. DCP was detected more frequently in groundwater samples collected in aerobic
C Timchalk et al.
Toxicology, 68(3), 291-306 (1991-01-01)
The objective of this study was to compare the disposition and metabolism of [14C]1,2-dichloropropane [( 14C]DCP) following oral and inhalation exposure since these two routes are of interest with regards to occupational and accidental exposure. [14C]DCP was administered orally to
A Trevisan et al.
Human & experimental toxicology, 12(2), 117-121 (1993-03-01)
1. Renal cortical slices isolated from the kidneys of male Wistar rats were used as an experimental model for studying the nephrotoxicity induced by 1,2-dichloropropane. 2. The solvent causes a depletion of renal reduced glutathione content and slight, but significant
H D Kirk et al.
Fundamental and applied toxicology : official journal of the Society of Toxicology, 28(1), 18-26 (1995-11-01)
1,2-Dichloropropane (PDC) was evaluated for its potential to cause embryonal/fetal toxicity and teratogenicity in pregnant rats and rabbits. PDC was administered via oral gavage at dose levels of 0, 10, 30, or 125 mg/kg/day on Days 6 through 15 of
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