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OXYPHENYL BUTAZONE

OXYPHENYL BUTAZONE Structure
OXYPHENYL BUTAZONE
  • CAS No.129-20-4
  • Chemical Name:OXYPHENYL BUTAZONE
  • CBNumber:CB2133346
  • Molecular Formula:C19H20N2O3
  • Formula Weight:324.37
  • MOL File:129-20-4.mol
OXYPHENYL BUTAZONE Property
Safety
Hazard and Precautionary Statements (GHS)
  • Symbol(GHS)
  • Signal wordWarning
  • Hazard statements H302-H400
  • Precautionary statements P273-P301+P312+P330
OXYPHENYL BUTAZONE Price More Price(2)
  • Brand: Sigma-Aldrich(India)
  • Product number: SML0540
  • Product name : Oxyphenbutazone
  • Purity: ≥98% (HPLC)
  • Packaging: 10MG
  • Price: ₹13996.73
  • Updated: 2022/06/14
  • Buy: Buy
  • Brand: Sigma-Aldrich(India)
  • Product number: SML0540
  • Product name : Oxyphenbutazone
  • Purity: ≥98% (HPLC)
  • Packaging: 50MG
  • Price: ₹54806.98
  • Updated: 2022/06/14
  • Buy: Buy

OXYPHENYL BUTAZONE Chemical Properties,Usage,Production

  • Chemical Properties Light Beige Solid
  • Originator Tanderil,Geigy,UK,1960
  • Uses Anti-inflammatory;Cyclooxygenase inhibito
  • Indications Oxyphenbutazone (Oxalid, Tandearil) is the principal uricosuric metabolite of phenylbutazone. It has the same indications and toxicities as phenylbutazone.
  • Definition ChEBI: A metabolite of phenylbutazone obtained by hydroxylation at position 4 of one of the phenyl rings. Commonly used (as its hydrate) to treat pain, swelling and stiffness associated with arthritis and gout, it was withdrawn from the market 1984 following asso iation with blood dyscrasis and Stevens-Johnson syndrome.
  • Manufacturing Process 43.2 parts of n-butyl malonic acid ethyl ester are added to a solution of 4.6 parts of sodium in 92 parts by volume of absolute alcohol. 39 parts of pbenzyloxy hydrazobenzene (MP 88° to 90°C) are added. About two-thirds of the alcohol is distilled off and 92 parts by volume of absolute xylene are added. Without removing the sloping condenser, the mixture is stirred for 12 hours at a bath temperature of 140° to 145°C. It is then cooled to 0° to 5°C, 100 parts of ice are added, the xylene is removed, the aqueous solution is extracted twice with chloroform and made acid to Congo red at 0° to 5°C with 6 N hydrochloric acid.
    The precipitate is taken up in chloroform, the solution obtained is washed twice with water, then with saturated salt solution, dried over Na2SO4and evaporated under vacuum (bath temperature 20°C). The residue is recrystallized from alcohol and produces 1-(p-benzyloxyphenyl)-2-phenyl-4-nbutyl-3,5-dioxo-pyrazolidine (C) as tiny white needles which melt at 132° to 133°C.
    16.6 parts of (C) are suspended in 166 parts by volume of ethyl acetate and, in the presence of 16.6 parts of Raney nickel, hydrogen is allowed to act at room temperature and atmospheric pressure.
    After 6 hours the calculated amount of hydrogen has been taken up. The residue obtained after filtering and evaporating is taken up in benzene and extracted twice with diluted sodium carbonate solution. The alkali extract is then made acid to Congo red with 6 N hydrochloric acid and the precipitate is taken up in ethyl acetate. The solution obtained is washed twice with salt solution, dried with sodium sulfate and evaporated. The residue is recrystallized from ether/petroleum ether. 1-(p-hydroxyphenyl)-2-phenyl-4-n Trade butyl-3,5-dioxo-pyrazolidine melts at 124° to 125°C.
  • brand name Tandearil (Novartis);Algi-tandril;Anarreumol-b;Artzone;Buteril;Campozim;Defolgin;Difmedol;Dolo-phlogase;Dolo-tandril;Fibutrox;Gp 40705;Iltazon;Iltoxon;Inflamil;Mindaril;Miyadril;Oflamin;Otone;Oxybutazone;Oxybutol;Oxyperol;Oxyphenbutone;Phlogistol;Phlogont;Phloguran;Pilabutina;Realin;Rheumapax;Segudol;Suganril;Tanal;Tandacot;Teneral;Vefren.
  • Therapeutic Function Antiinflammatory
  • World Health Organization (WHO) Oxyphenbutazone, a pyrazolone derivative with anti-inflammatory, analgesic and antipyretic activity, was introduced in 1955 for the treatment of rheumatic disorders. It is one of the active metabolites of phenylbutazone and has a similar spectrum of activity including an association with serious and sometimes fatal adverse reactions, notably cases of aplastic anaemia and agranulocytosis. Many national drug regulatory authorities consider that more recently introduced drugs offer a safer alternative for most, if not all, patients requiring antiinflammatory agents. Although oxyphenbutazone has been widely withdrawn it remains available in some countries.
  • General Description Oxyphenbutazone is a derivative compound of phenylbutazone. Oxyphenbutazone is one of the metabolites formed in the liver following administration of phenylbutazone. Given orally it causes fewer gastrointestinal adverse effects than phenylbutazone and is used at 300 – 400 mg/d for the same indications as the parent drug.
  • Biochem/physiol Actions Oxyphenbutazone is a non-steroid anti inflammatory; anti Mycobacterium tuberculosis agent. Oxyphenbutazone is known to cause inflammatory effects on tissues. Oxyphenbutazone, as a drug, decreases cellular exudates, without involving the pituitary-adrenal axis or the immunity response. Though the drug delivers a number of side effects, it is considered to be less toxic than phenylbutazone, due to decreased rate of intestinal absorption.
  • Clinical Use Oxyphenbutazone is a nonsteroidal anti-inflammatory drug, which was used by oral, rectal, or topical administration (400 - 600 mg/d) for the acute treatment of ankylosing spondylitis, chronic polyarthritis, and gout. Because of a high incidence of severe side effects including disturbances of the hematopoietic system like agranulocytosis and aplastic anemia the compound is no longer used. Oxyphenbutazone is a metabolite of phenylbutazone.
OXYPHENYL BUTAZONE Preparation Products And Raw materials
Raw materials
Preparation Products
OXYPHENYL BUTAZONE Suppliers
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OXYPHENYL BUTAZONE Spectrum
129-20-4, OXYPHENYL BUTAZONERelated Search:
  • Pharmaceuticals
  • Intermediates & Fine Chemicals
  • Heterocycles
  • Aromatics
  • Active Pharmaceutical Ingredients
  • 抑制剂
  • 抗炎镇痛药物
  • C19H20N2O3
  • 化合物 T16419
  • 羟基保泰松溶液,100PPM
  • 羟基保泰松,坦特利尔,羟保松
  • 羟基保泰松
  • 羟布宗
  • 羟保松
  • 129-20-4
  • Phenelzine Impurity 10
  • Oxyphenbutazone in acetonitrile
  • Oxyphenbutazone Solution, 100ppm
  • OXYPHENYL BUTAZONE USP/EP/BP
  • OxyphenbutazoneQ: What is Oxyphenbutazone Q: What is the CAS Number of Oxyphenbutazone Q: What is the storage condition of Oxyphenbutazone Q: What are the applications of Oxyphenbutazone
  • Butaflogin
  • bm1
  • BM 1
  • Artroflog
  • 4-Butyl-2-(p-hydroxyphenyl)-1-phenyl-3,5-pyrazolidinedione
  • 4-Butyl-2-(4-hydroxyphenyl)-1-phenyl-3,5-dioxopyrazolidine
  • 4-butyl-1-(p-hydroxyphenyl)-2-phenyl-5-pyrazolidinedione
  • 4-Butyl-1-(p-hydroxyphenyl)-2-phenyl-3,5-pyrazolidinedione
  • 4-Butyl-1-(4-hydroxyphenyl)-2-phenyl-3,5-pyrazolidinedione
  • 3,5-pyrazolidinedione,4-butyl-1-(4-hydroxyphenyl)-2-phenyl
  • 3,5-Pyrazolidinedione, 4-butyl-1-(p-hydroxyphenyl)-2-phenyl-
  • 3,5-Pyrazolidinedione, 4-butyl-1-(4-hydroxyphenyl)-2-phenyl-
  • 3,5-Dioxo-1-phenyl-2-(p-hydroxyphenyl)-4-N-butylpyrazolidene
  • 1-p-hydroxyphenyl-2-phenyl-3,5-dioxo-4-n-butylpyrazolidine
  • 1-phenyl-2-(p-hydroxyphenyl)-3,5-dioxo-4-n-butylpyrazolidine
  • 1-Phenyl-2-(p-hydroxyphenyl)-3,5-dioxo-4-butylpyrazolidine
  • 1-(p-hydroxyphenyl)-2-phenyl-4-butylpyrazolidine-3,5-dione
  • 1-(p-Hydroxyphenyl)-2-phenyl-4-butyl-3,5-pyrazolidinedione
  • 1-(p-Hydroxyphenyl)-2-phenyl-3,5-dioxo-4-N-butylpyrazolidine
  • OXYPHENYL BUTAZONE
  • LABOTEST-BB LT00134684
  • Ro 04-4410
  • NSC 526053
  • 4-Butyl-1-(4-hydroxyphenyl)-2-phenyl-
  • 4-butyl-1-(4-hydroxyphenyl)-2-phenyl-pyrazolidine-3,5-quinone
  • 4-butyl-1-(4-hydroxyphenyl)-2-phenylpyrazolidine-3,5-dione
  • 4-butyl-1-(4-hydroxyphenyl)-2-phenyl-pyrazolidine-3,5-dione
  • Grovaril
  • Hydroxy phenylbutazone
  • PARAHYDROXY-PHENYLBUTAZONE
  • 4-Hydroxyphenylbutazone
  • Visubutina
  • Valioil
  • usafge-14
  • USAF Ge-14
  • Tendearil
  • Telidal
  • telidac

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