850608
Diphenyl phosphate
99%
Synonyme(s) :
Diphenyl hydrogen phosphate
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A propos de cet article
Formule linéaire :
(C6H5O)2P(O)OH
Numéro CAS:
Poids moléculaire :
250.19
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
212-657-2
Beilstein/REAXYS Number:
1379164
MDL number:
Assay:
99%
Form:
crystals
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99%
form
crystals
mp
62-66 °C (lit.)
functional group
phosphate
SMILES string
OP(=O)(Oc1ccccc1)Oc2ccccc2
InChI
1S/C12H11O4P/c13-17(14,15-11-7-3-1-4-8-11)16-12-9-5-2-6-10-12/h1-10H,(H,13,14)
InChI key
ASMQGLCHMVWBQR-UHFFFAOYSA-N
Application
Diphenyl phosphate can be used as an organic catalyst for the ring-opening polymerization (ROP) of renewable 5-alkyl δ-lactones. In combination with zinc iodide, it forms a novel initiating system for the living cationic polymerization of isobutyl vinyl ether.
Classe de stockage
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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Xiao Yan et al.
Chemosphere, 200, 569-575 (2018-03-06)
Urinary metabolites of phosphate flame retardants (PFRs) were determined in workers from an electronic waste (e-waste) recycling site and an incineration plant, in order to assess the PFR exposure risks of workers occupied with e-waste recycling and incineration. Bis(2-chloroethyl) phosphate
Living cationic polymerization of isobutyl vinyl ether by the diphenyl phosphate/zinc iodide initiating system.
Sawamoto M, et al.
Polym. Bull., 20(5), 407-412 (1988)
Zongrui Li et al.
Environmental pollution (Barking, Essex : 1987), 262, 114260-114260 (2020-03-03)
A substantial increase in the usage of organophosphate esters (OPEs) as flame retardants and plasticizers in rubbers, textiles, upholstered furniture, lacquers, plastics, building materials and electronic equipment has resulted in their increasing concentrations in the environment over time. However, little