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Эдрофония хлорид
- английское имяEdrophonium chloride
- CAS №116-38-1
- CBNumberCB1170926
- ФормулаC10H16ClNO
- мольный вес201.69
- EINECS204-138-4
- номер MDLMFCD00055064
- файл Mol116-38-1.mol
химическое свойство
Температура плавления | 162-163 °C (decomp) |
плотность | 1.0787 (rough estimate) |
показатель преломления | 1.6000 (estimate) |
температура хранения | Inert atmosphere,Room Temperature |
растворимость | Very soluble in water, freely soluble in ethanol (96 per cent), practically insoluble in methylene chloride. |
форма | A crystalline solid |
цвет | White to light yellow |
ИнЧИКей | BXKDSDJJOVIHMX-UHFFFAOYSA-N |
Справочник по базе данных CAS | 116-38-1(CAS DataBase Reference) |
FDA UNII | QO611KSM5P |
Код УВД | V04CX07 |
UNSPSC Code | 41116107 |
NACRES | NA.24 |
WGK Германия | 3 |
RTECS | BQ5870000 |
кода HS | 2923900100 |
Токсичность | mouse,LD50,intraperitoneal,30mg/kg (30mg/kg),Pharmaceutical Chemistry Journal Vol. 10, Pg. 327, 1976. |
Эдрофония хлорид химические свойства, назначение, производство
Химические свойства
White or almost white, crystalline powderИспользование
Pharmacologically, edrophonium is also similar to neostigmine; however, it begins to act quicker and is shorter lasting.Использование
A reversible Acetylcholinesterase inhibitor.Определение
ChEBI: The chloride salt of edrophonium. A reversible inhibitor of cholinesterase with a rapid onset (30-60 seconds after injection) but a short duration of action (5-15 minutes), it is used in myasthenia gravis both diagnostically and to distinguish between unde - or over-treatment with other anticholinesterases. It has also been used for the reversal of neuromuscular blockade in anaesthesia, and for the management of poisoning due to tetrodotoxin, a neuromuscular blocking toxin found in puffer fish and other mari e animals.Общее описание
Edrophonium chloride,ethyl(m-hydroxyphenyl)dimethylammonium chloride(Tensilon), is a reversible anticholinesterase agent. It isbitter and very soluble in water and alcohol. Edrophoniumchloride injection has a pH of 5.2 to 5.5. On parenteral administration,edrophonium has a more rapid onset andshorter duration of action than neostigmine, pyridostigmine,or ambenonium. It is a specific anticurare agent andacts within 1 minute to alleviate overdose of d-tubocurarine,dimethyl d-tubocurarine, or gallamine triethiodide.Клиническое использование
Edrophonium Chloride is also used to terminate the action of any one ofthese drugs when the physician so desires. It is of no value,however, in terminating the action of the depolarizing (i.e.,noncompetitive) blocking agents, such as decamethoniumand succinylcholine. In addition to inhibiting AChE, edrophoniumchloride has a direct cholinomimetic effect onskeletal muscle, which is greater than that of most otheranticholinesterase drugs.Синтез
Edrophonium, ethyl-(3-hydroxyphenyl)dimethylammonium chloride (13.2.13), is made by reacting 3-dimethylaminophenol with ethylbromide, which forms ethyl(3-hydroxyphenyl)dimethylammonium bromide (13.2.12), the bromine atom of which is replaced with a chlorine atom by reacting it with silver chloride, giving edrophonium (13.2.13) [45].Эдрофония хлорид запасные части и сырье
Эдрофония хлорид поставщик
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