Bis(4-cyanophenyl) phenyl phosphate as viscosity reducing comonomer for phthalonitrile resins

2019 ◽  
Vol 139 ◽  
pp. 34-41 ◽  
Author(s):  
V.E. Terekhov ◽  
V.V. Aleshkevich ◽  
E.S. Afanaseva ◽  
S.S. Nechausov ◽  
A.V. Babkin ◽  
...  
Keyword(s):  
2021 ◽  
Vol 1238 ◽  
pp. 130389
Author(s):  
Farzane Pazoki ◽  
Razieh Esfandiarpour ◽  
Fatemeh Mohsenzadeh ◽  
Fahimeh Mohammadpanah ◽  
Akbar Heydari

1990 ◽  
Vol 73 (6) ◽  
pp. 842-849 ◽  
Author(s):  
Richard M Rocco

Abstract Official methods for the measurement of alkaline phosphatase (ALP) in dairy products use either phenyl phosphate or phenolphthaleln monophosphate as substrate. Quantitation of results requires butanol extraction of the Indophenol (Scharer) or 3-h dialysis of the liberated phenolphthaleln (Rutgers). The Advanced Fluorophos® assay Is based on a self-indicating substrate which, when acted upon by ALP, loses a phosphate radical and becomes a highly fluorescent compound. The rate of fluorophore formation Is monitored for 3 mln In a fluorometer and the enzyme activity In mU/L Is calculated. Eight laboratories participated in a collaborative study to evaluate the Fluorophos® assay for determining ALP activity In whole milk, skim milk, chocolate milk, and cream (half and half). The comparative method was the AOAC quantitative phenyl phosphate method, 16.121-16.122 (14th Ed.). Mixed herd raw milk was added to pasteurized samples at 0.05, 0.1, and 0.2% (v/v). Method performance at 0.1% (v/v) added raw milk as measured by repeatability and reproducibility standard deviations (sr and sR) and relative standard deviations (RSDr and RSDR), respectively, were: whole milk, sr = 21.7%, sR = 34.6%, RSDr = 4.4%, RSDR = 7.0%; skim milk, sr = 19.2%, sR = 31.4%, RSDr = 3.8%, RSDR = 6.2%; chocolate milk, sr = 27.6%, sR = 45.8%, RSDr = 5.3%, RSDR = 8.8%. The method has been adopted official first action by AOAC for determination of alkaline phosphatase in whole milk, skim milk, and chocolate milk.


Author(s):  
S. Reinoso ◽  
P. Vitoria ◽  
M. Ugalde ◽  
J. M. Gutiérrez-Zorrilla ◽  
A. Luque ◽  
...  
Keyword(s):  

1991 ◽  
Vol 44 (6) ◽  
pp. 771 ◽  
Author(s):  
JW Perich ◽  
RM Valerio ◽  
PF Alewood ◽  
RB Johns

A solid phase method is described for the synthesis of O- phosphoseryl-containing peptides by the use of polystyrene resin (Merrifield) as the peptide support and protected Boc-Ser(PO3R2)-OH derivatives for the incorporation of the phosphorylated seryl residue. The viability of this solid phase approach was demonstrated by the synthesis of HBr.H-Glu-Ser (PO3Et2)-Leu-OH in high yield by the use of Bo -Ser(PO3Et2)-OH in peptide synthesis and subsequent use of HBr/CF3CO2H for cleavage of the Ser(PO3Et2)-containing tripeptide from the resin support. Similarly, the dipeptide, CF3CO2H.H-Ser(P)- Leu -OH, was prepared in high yield by using Boc -Ser(PO3But2)-OH in peptide synthesis followed by the one-step deprotection of the Ser(PO3But2)- dipeptide resin by treatment with HBr/CF3CO2H (90 min). Alternatively, the O-phosphoseryl tripeptide , CF3CO2H.H-Glu-Ser(P)- Leu -OH was prepared by using either Ppoc -Ser(PO3Bzl2)-OH or Boc-Ser(PO3Ph2)-OH in peptide synthesis. The one-step deprotection of the Ser(PO3Bzl2)-containing tripeptide and cleavage of the peptide from the resin support was effected by high-pressure hydrogenolysis (palladium acetate). In the case of phenyl phosphate protection, the Ser(PO3Ph2)-containing peptide was cleaved from the resin support by high-pressure hydrogenolysis (palladium acetate) followed by cleavage of the phenyl phosphate groups by platinum-mediated hydrogenolysis (1.0 equiv. PtO2/phenyl group) in 50% CF3CO2H/AcOH.


1981 ◽  
Vol 34 (8) ◽  
pp. 1769 ◽  
Author(s):  
DA Buckingham ◽  
CR Clark

Tracer 18O studies have established that base hydrolysis of coordinated acetyl phosphate in [(NH3)5Co-OPO3COCH3]+ (kOH 0.53 mol-1 dm3 s-1, 25°C, I 1.0 NaClO4) proceeds with exclusive carbon-oxygen bond fission. The hydrolysis of acetyl phenyl phosphate monoanion is significantly catalysed by the exchange-inert hydroxo complex [(NH3)5Co-OH]2+ (kMOH 2.9 × 10-2 mol-1 dm3 s-1, 25°) which operates through a nucleophilic pathway involving attack at carbonyl carbon.


1991 ◽  
Vol 16 (1) ◽  
pp. 117-127
Author(s):  
CHARLES E. HEALY ◽  
RASHMI S. NAIR ◽  
JOAN K. LEMEN ◽  
FREDERICK R. JOHANNSEN

2009 ◽  
Vol 44 (2) ◽  
pp. 328-333 ◽  
Author(s):  
Hidekazu Tanaka ◽  
Takeshi Okumiya ◽  
Shun-kichi Ueda ◽  
Yukihiko Taketani ◽  
Masahiko Murakami

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