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Дроперидол
- английское имяDROPERIDOL
- CAS №548-73-2
- CBNumberCB9145418
- ФормулаC22H22FN3O2
- мольный вес379.43
- EINECS208-957-8
- номер MDLMFCD00083290
- файл Mol548-73-2.mol
химическое свойство
Температура плавления | 148-149°C |
плотность | 1.2154 (estimate) |
температура хранения | 2-8°C |
растворимость | Practically insoluble in water, freely soluble in dimethylformamide and in methylene chloride, sparingly soluble in ethanol (96 per cent). |
форма | Solid |
пка | 7.64(at 25℃) |
цвет | Pale Yellow to Pale Beige |
Растворимость в воде | 4.1mg/L(30 ºC) |
Справочник по базе данных CAS | 548-73-2(CAS DataBase Reference) |
Словарь онкологических терминов NCI | droperidol |
FDA UNII | O9U0F09D5X |
Словарь наркотиков NCI | droperidol |
Код УВД | N05AD08 |
Система регистрации веществ EPA | 2H-Benzimidazol-2-one, 1-[1-[4-(4-fluorophenyl)-4-oxobutyl]-1,2,3,6-tetrahydro-4-pyridinyl]-1,3-dihydro- (548-73-2) |
UNSPSC Code | 41116107 |
NACRES | NA.77 |
Коды опасности | Xn | |||||||||
Заявления о рисках | 22 | |||||||||
Заявления о безопасности | 36 | |||||||||
РИДАДР | 3249 | |||||||||
WGK Германия | 3 | |||||||||
RTECS | DE2100000 | |||||||||
Класс опасности | 6.1(b) | |||||||||
Группа упаковки | III | |||||||||
кода HS | 2933995800 | |||||||||
Банк данных об опасных веществах | 548-73-2(Hazardous Substances Data) | |||||||||
Токсичность | LD50 oral in rat: 750mg/kg | |||||||||
NFPA 704: |
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рисовальное письмо(GHS)
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рисовальное письмо(GHS)
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сигнальный язык
предупреждение
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вредная бумага
H302:Вредно при проглатывании.
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оператор предупредительных мер
P301+P312+P330:ПРИ ПРОГЛАТЫВАНИИ: Обратиться за медицинской помощью при плохом самочувствии. Прополоскать рот.
Дроперидол химические свойства, назначение, производство
Описание
D roperidol is a butyrophenone that has potent antidopaminergic (D2) activity and mild α2-blocking actions. It produces sedation and anxiolysis and is an effective antiemetic. A dverse effects include vasodilatation and hypotension, and at higher doses, dystonic reactions can occur. D roperidol was used for premedication and in neuroleptanaesthesia until reports of death from long QT syndrome led to its withdrawal in 2001. It has recently been reintroduced and licenced at lower doses for prevention of postoperative nausea and vomiting. D roperidol has an onset of 3–10 min after i.v. injection and duration of action of 6–12h. It undergoes hepatic metabolism, but approximately 10% of the drug is excreted unchanged in the urine.Химические свойства
Pale Yellow SolidИспользование
The neuroleptic droperidol possesses antipsychotic, sedative, and antishock action. It potentiates the action of drugs for narcosis. In psychiatric practice, droperidol is used for psychomotor excitement and hallucinations. The principal use of this drug lies in anesthesiology for neuroleptanalgesia in combination with fentanyl. It is used in premedication as well as in surgical operations and post-operational circumstances.Определение
ChEBI: An organofluorine compound that is haloperidol in which the hydroxy group has been eliminated with the introduction of a double bond in the piperidine ring, and the 4-chlorophenyl group has been replaced by a benzimidazol-2-on-1-yl group. It is used in the management of chemotherapy-induced nausea and vomiting, and in conjunction with an opioid analgesic such as fentanyl to maintain the patient in a calm state of neuroleptanalgesia with indifference to surroundings but still able to cooperate with the surgeo .Общее описание
Droperidol, 1-{1-[3-(p-fluorobenzoyl)propyl]-1,2, 3,6-tetrahydro-4-pyridyl}-2-benzimidazolinone(Inapsine), may be used alone as a preanestheticneuroleptic or as an antiemetic. Because of its very shortactingand highly sedating properties, its most frequent useis in combination (Innovar) with the narcotic agent fentanyl(Sublimaze) preanesthetically.Дроперидол запасные части и сырье
Дроперидол поставщик
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