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苄基三苯基氯化磷

规格或纯度: 99%

CAS编号: 1100-88-5
分子式: C₂₅H₂₂ClP
分子量: 388.87
Beilstein号: 3599868
EC号: 214-154-3
MDL号: MFCD00011913
PubChem编号: 70671

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货号 (SKU)	包装规格	是否现货	价格	数量
B109283-25g	25g	现货
B109283-100g	100g	现货
B109283-250g	250g	现货
B109283-500g	500g	现货
B109283-2.5kg	2.5kg	现货

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元素分类的化合物磷化合物

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基本描述

规格或纯度	99%
英文名称	Benzyltriphenylphosphonium chloride
别名	三苯基苄基氯化膦\|磷盐“P”,BPP\|三苯基(苯基甲基)氯化鏻\|苄基三苯基氯化鏻\|苄基三苯基氯化膦
英文别名	Benzyltriphenylphosphonium chloride\|1100-88-5\|Triphenylbenzylphosphonium chloride\|Phosphonium, triphenyl(phenylmethyl)-, chloride\|MFCD00011913\|Phosphonium, benzyltriphenyl-, chloride\|benzyl(triphenyl)phosphanium;chloride\|benzyl(triphenyl)phosphonium chlor
应用	与双酚AF配合用于氟橡胶的硫化剂。 Benzyltriphenylphosphonium chloride can be used as a reactant for the synthesis of: · Platinum chloro-tetrazole complexes via azidation. · Trans-stilbenes and cinnamates via Wittig olefination。 · Achiral N-hydroxyformamide inhibitors of ADAM-TS4 and ADAM-TS5 for osteoarthritis treatment. · Pentiptycenes for use as light-driven molecular brakes. · Archipelago structures for formation of petroleum asphaltenes. It is also used as a crosslinking agent for tube-like natural halloysite / fluorelastomer nanocomposites. Crosslinking agent for tube-like natural halloysite / fluorelastomer nanocomposites Reactant for synthesis of: · Platinum chloro tetrazole complexes via azidation · Trans-stilbenes and cinnamates via Wittig olefination · Achiral N-hydroxyformamide inhibitors of ADAM-TS4 and ADAM-TS5 for osteoarthritis treatment · Pentiptycenes for use as light-driven molecular brakes Reactant for formation of archipelago structures for formation of p
储存温度	充氩
运输条件	常规运输
产品介绍	溶于水，溶于氯仿,微溶于低分子量的脂肪族醇。热分解温度＞323℃，略带苄基味。与双酚AF配合用于氟橡胶的硫化剂。 Benzyltriphenylphosphonium chloride can be used as a reactant for the synthesis of: · Platinum chloro-tetrazole complexes via azidation. · Trans-stilbenes and cinnamates via Wittig olefination。 · Achiral N-hydroxyformamide inhibitors of ADAM-TS4 and ADAM-TS5 for osteoarthritis treatment. · Pentiptycenes for use as light-driven molecular brakes. · Archipelago structures for formation of petroleum asphaltenes. It is also used as a crosslinking agent for tube-like natural halloysite / fluorelastomer nanocomposites. Crosslinking agent for tube-like natural halloysite / fluorelastomer nanocomposites Reactant for synthesis of: · Platinum chloro tetrazole complexes via azidation · Trans-stilbenes and cinnamates via Wittig olefination · Achiral N-hydroxyformamide inhibitors of ADAM-TS4 and ADAM-TS5 for osteoarthritis treatment · Pentiptycenes for use as light-driven molecular brakes Reactant for formation of archipelago structures for formation of p

名称和标识符

EC号	214-154-3
IUPAC Name	benzyl(triphenyl)phosphanium;chloride
INCHI	InChI=1S/C25H22P.ClH/c1-5-13-22(14-6-1)21-26(23-15-7-2-8-16-23,24-17-9-3-10-18-24)25-19-11-4-12-20-25;/h1-20H,21H2;1H/q+1;/p-1
InChi Key	USFRYJRPHFMVBZ-UHFFFAOYSA-M
Canonical SMILES	C1=CC=C(C=C1)C[P+](C2=CC=CC=C2)(C3=CC=CC=C3)C4=CC=CC=C4.[Cl-]
分子式	C₂₅H₂₂ClP
UN Number	2811
PubChem CID	70671
Beilstein号	3599868
分子量	388.87

化学和物理性质

溶解性	Soluble in water and alcohol. Insoluble in acetone
敏感性	对湿度敏感;对光敏感
熔点	300°C
闪点(℉)	572 °F
闪点(℃)	300 °C

安全信息

象形图	Toxic Health Hazard Environmental Hazard Corrosive Harmful
信号词	Danger
危险声明	H315: Causes skin irritation H319: Causes serious eye irritation H335: May cause respiratory irritation H301: Toxic if swallowed H311: Toxic in contact with skin H331: Toxic if inhaled H318: Causes serious eye damage H400: Very toxic to aquatic life H410: Very toxic to aquatic life with long lasting effects H300: Fatal if swallowed H330: Fatal if inhaled H372: Causes damage to organs through prolonged or repeated exposure
预防措施声明	P261,P305+P351+P338,P273,P280,P302+P352,P321,P405,P501,P264,P260,P284,P271,P270,P304+P340,P403+P233,P362+P364,P391,P330,P320,P361+P364,P264+P265,P301+P316,P305+P354+P338,P317,P337+P317,P332+P317,P316,P319
WGK Germany	3
RTECS	TA2416500
Reaxy-Rn	3599868
个人防护装备	Eyeshields,Faceshields,Gloves,type P2 (EN 143) respirator cartridges

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