蒸汽压
23.32 psi ( 55 °C)
6.58 psi ( 20 °C)
表单
liquid
浓度
2.0 M in methylene chloride
密度
1.363 g/mL at 25 °C
SMILES字符串
ClP(Cl)Cl
InChI
1S/Cl3P/c1-4(2)3
InChI key
FAIAAWCVCHQXDN-UHFFFAOYSA-N
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警示用语：
Danger
危险分类
Acute Tox. 2 Inhalation - Acute Tox. 3 Oral - Carc. 2 - Eye Dam. 1 - Skin Corr. 1A - STOT RE 2 Inhalation - STOT SE 3
靶器官
Central nervous system, Respiratory Tract
补充剂危害
储存分类代码
6.1B - Non-combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
WGK
WGK 2
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
法规信息
新产品
此项目有
L Yu et al.
Amino acids, 28(4), 369-372 (2005-05-13)
The reactions of phosphorus trichloride with various amino acids afford the pentacoordinated spirophosphoranes. The reaction procedures were traced by (31)P NMR spectra techniques. A new crystal structure of alanine derivative was characterized, which is a slightly distorted TBP structure. Besides
T Kapias et al.
Journal of hazardous materials, 81(3), 223-249 (2001-02-13)
Phosphorus trichloride and oxychloride are aggressive materials, widely used in the process industries. On escape to the atmosphere they create toxic clouds that may cause serious damage to people and to the environment. When spilled onto the ground they create
A Eldad et al.
Burns : journal of the International Society for Burn Injuries, 18(4), 340-341 (1992-08-01)
A 51-year-old chemical engineer sustained phosphorous pentachloride partial skin thickness burns over 20 per cent of his body surface area. Although macroscopically and microscopically the wound seemed to be superficial, the course of clinical healing of this injury was very
Petri A Turhanen et al.
Organic & biomolecular chemistry, 1(18), 3223-3226 (2003-10-07)
Methods for the preparation of mixed tetra-amide esters 1 and 2, the partial amide ester 3, and tri- and P,P-diamides 4 and 5 from monophosphorus spieces 12, 8 and 9, respectively, were developed. Compounds 8 and 9 were obtained from
Phosphorus trichloride-mediated and microwave-assisted synthesis of a small collection of amides bearing strong electron-withdrawing group substituted anilines.
Matteo Colombo et al.
Journal of combinatorial chemistry, 11(3), 335-337 (2009-03-31)
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