Benzyltriphenylphosphonium chloride
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Benzyltriphenylphosphonium chloride
structure -
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CAS No:
1100-88-5
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Formula:
C25H22P.Cl
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Chemical Name:
Benzyltriphenylphosphonium chloride
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Synonyms:
Phosphonium,triphenyl(phenylmethyl)-,chloride (1:1);Phosphonium,benzyltriphenyl-,chloride;Benzyltriphenylphosphonium chloride;Phosphonium,triphenyl(phenylmethyl)-,chloride;Triphenylbenzylphosphonium chloride;GM 200;NSC 116712;BTPPC;BPP;TPP-ZC;13246-50-9;127463-89-2;917100-19-7;1927850-93-8
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CAS No:
Description
Benzyltriphenylphosphonium chloride is white to off-white crystals, soluble in water, with a melting point of 337°C, a flash point of 300°C, a density of 1.18 g/cm3 (20°C), a vapor pressure of 0.1 hPa, a flash point of 300°C, and a molecular weight of 388.869. It is chemically stable and incompatible with strong oxidants.
Benzyltriphenylphosphonium chloride Basic Attributes
388.87
388.115
3599868
214-154-3
116712
DTXSID6051566
29310095
Characteristics
0
2.18470
White to almost white Crystalline Powder
1.18 g/cm3 (20℃)
314-315 °C
300°C
SOLUBLE
Store at<= 20°C.
0.1 hPa
LD50 orally in Rabbit: 43 mg/kg
Safety Information
II
6.1
UN 2811 6.1/PG 2
3
25-36/37/38-24/25
26-36/37/39-45-36
TA2416500
T,Xi
Stable. Incompatible with strong oxidizing agents.
P260, P261, P264, P270, P271, P280, P284, P301+P310, P302+P352, P304+P340, P305+P351+P338, P310, P311, P312, P314, P320, P321, P322, P330, P332+P313, P337+P313, P361, P362, P363, P403+P233, P405, P501
H300
|Danger|H300 (76.32%): Fatal if swallowed [Danger Acute toxicity, oral]|P260, P261, P264, P270, P271, P273, P280, P284, P301+P310, P302+P352, P304+P340, P305+P351+P338, P310, P311, P312, P314, P320, P321, P322, P330, P332+P313, P337+P313, P361, P362, P363, P391, P403+P233, P405, and P501|Aggregated GHS information provided by 267 companies from 25 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
Benzyltriphenylphosphonium chloride Use and Manufacturing
Benzyltriphenylphosphonium chloride is used as an organic synthesis reagent for several compounds, including stable phosphine ylides containing saturated oxygen heterocycles, and is also used to synthesize new substituted cis-stilbene derivatives with antibacterial activity. Benzyltriphenylphosphonium chloride is used in combination with bisphenol AF as a vulcanizing agent for fluororubber.
Phosphonium, triphenyl(phenylmethyl)-, chloride (1:1): ACTIVE
Computed Properties
Molecular Weight:388.9
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:5
Exact Mass:388.1147654
Monoisotopic Mass:388.1147654
Heavy Atom Count:27
Complexity:347
Covalently-Bonded Unit Count:2
Compound Is Canonicalized:Yes
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Benzyltriphenylphosphonium chloride
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