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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1957463Erstellt: 26. Oktober 2026

Phenylmethylsulfonyl Fluoride → Tromethamine hydrochloride

https://huagongshe.com/reaction/1957463

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPhenylmethylsulfonyl FluorideHCID 4784—
EduktChloramphenicolHCID 5959—
EduktParaoxonHCID 9395—
EduktLeupeptin acidHCID 189069—
EduktTris HCl EDTAHCID 86752936—
LösungsmittelWaterHCID 962—
LösungsmittelIsopropanolHCID 3776—
ProduktTromethamine hydrochlorideHCID 93573—

Reaktionsschritte

Leupeptin and aprothinin (from Boerhinger) stock solutions (0.1%) for each weigh out 0.0025 g and add both to 2.5 mL of distilled water. Mix, aliquot and store at -20° C. for up to 6 months or store 1 week at 4° C.; Phenylmethylsulfonylfluoride stock solution (PMSF) 10 mg/mL, prepared from 0.05 g of PMSF and 5 mL of isopropanol (Store in the dark at room temperature for up to 1 year); Complete homogenation buffer (from Tris HCl/EDTA buffer (100 mL), PMSF stock (350 μL, final concentration of 35 μg/mL), and leupeptin/aprotinin stock (50 μL, final concentration of 0.5 μL/mL)); BSA buffer, prepared from complete homogenation buffer+2 mg/mL BSA, fraction V; n-butyryl co-enzyme A (Sigma B1508 lyophilized powder diluted to 5 mg/mL and stored at -20° C. in small aliquots to avoid excessive freeze-thawings); CAT enzyme (Sigma C8413 chloramphenicol acetyltransferase); 14C-chloramphenicol (NEN NEC-408A chloramphenicol, D-threo-[dichloroacetyl-1,2-14C]-CAT assay grade (TLC based), stored at 4° C. and diluted 1:10 in BSA buffer just prior to use); mixed xylenes (Aldrich); paraoxon (diethyl-n-nitrophenyl phosphate, from Sigma is a liquid with 90% purity) stock solution is prepared by diluting the original liquid 1:80 in isopropanol (Note: To achieve a final paraoxon concentration of 5 μM in a 130 μL of reaction mixture, a further 1:200 dilution in homogenization buffer is made and 3.3 μL of this 0.8 mM paraoxon solution is added to the reaction mixture); BCA protein reagent.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05785992
Quelldatensatzuspto-grants-1998_07
ORD IDord-ea779df32e7b4498a8f4bfca98cb8bf3
Quellennotizuspto-grants-1998_07