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3-гидрокситирамин гидрохлорид

3-гидрокситирамин гидрохлорид структура
62-31-7
CAS №
62-31-7
Химическое название:
3-гидрокситирамин гидрохлорид
английское имя:
Dopamine hydrochloride
Синонимы:
DOPAMINE HYDROCHLORIDE;DOPAMINE HCL;2-(3,4-DIHYDROXYPHENYL)ETHYLAMINE HYDROCHLORIDE;ASL-279;intropin;Dopamin Hcl;dopaminechloride;DOPAMINE HCL(RG);Dopamine solution;3-Hydroxytyramine, HCl
CBNumber:
CB9243534
Формула:
C8H12ClNO2
молекулярный вес:
189.64
MOL File:
62-31-7.mol

3-гидрокситирамин гидрохлорид атрибут

Температура плавления: 248-250 °C(lit.)
плотность: 1.4 g/cm3
Fp: 11℃
температура хранения: Store below +30°C.
растворимость: алкоголь: 20 мг/мл
форма: Кристаллический порошок
цвет: Легкий загар
Растворимость в воде: растворимый
Чувствительный: Air & Light Sensitive
Мерк: 14,8462
БРН: 3656720
Стабильность:: Стабильный. Несовместим с сильными окислителями. Горючий.
ИнЧИКей: CTENFNNZBMHDDG-UHFFFAOYSA-N
Справочник по базе данных CAS: 62-31-7(CAS DataBase Reference)
Рейтинг продуктов питания EWG: 1
FDA UNII: 7L3E358N9L
Система регистрации веществ EPA: 1,2-Benzenediol, 4-(2-aminoethyl)-, hydrochloride (62-31-7)
безопасность
  • Заявления о рисках и безопасности
  • код информации об опасности(GHS)
Коды опасности Xi,N,Xn,T,F
Заявления о рисках 36/37/38-50/53-22-39/23/24/25-23/24/25-11
Заявления о безопасности 26-36-61-45-36/37-16
РИДАДР UN1230 - class 3 - PG 2 - Methanol, solution
WGK Германия 2
RTECS UX1092000
F 8-10-23
Примечание об опасности Irritant
TSCA Yes
кода HS 29222900
Токсичность LD50 orally in Rabbit: 2859 mg/kg
символ(GHS) GHS hazard pictograms
сигнальное слово Warning
Заявление об опасности
пароль Заявление об опасности Класс опасности категория сигнальное слово пиктограмма предупреждение
H302 Вредно при проглатывании. Острая токсичность, пероральная Категория 4 Предупреждение GHS hazard pictograms P264, P270, P301+P312, P330, P501
Внимание
P301+P312+P330 ПРИ ПРОГЛАТЫВАНИИ: Обратиться за медицинской помощью при плохом самочувствии. Прополоскать рот.

3-гидрокситирамин гидрохлорид MSDS


3-Hydroxytyramine hydrochloride

3-гидрокситирамин гидрохлорид химические свойства, назначение, производство

Описание

Dopamine (hydrochloride) is an endogenous catecholamine neurotransmitter synthesized from the amino acid L-tyrosine that acts as an agonist at dopamine receptors (D1-5). Dopamine is mainly synthesized in the substantia nigra and ventral tegmental area, and is a precursor in norepinephrine and epinephrine biosynthesis. Dopamine-containing neurons in the brain are involved in reward-motivated behavior, motor control, and hormone release. Dopamine is also synthesized in the adrenal glands where it exerts peripheral paracrine functions including control of vasodilation, sodium excretion, insulin production, gastrointestinal motility, and the activity of lymphocytes. Loss or damage of dopaminergic neurons in the substantia nigra is associated with Parkinson’s disease.

Химические свойства

Dopamine hydrochloride is designated chemically as 3,4-dihydroxyphenethylamine hydrochloride, a white crystalline powder freely soluble in water. It can also be dissolved in hot 95% ethanol, methanol, and sodium hydroxide solution. However, it is insoluble in chloroform, ether, and benzene. It has no odor and a slightly bitter taste. Dopamine (also referred to as 3-hydroxytyramine) is a naturally occurring biochemical catecholamine precursor of norepinephrine.

Использование

Endogenous catecholamine with α and β-adrenergic activity. Cardiotonic; antihypotensive.

Подготовка

Dopamine hydrochloride is produced through the ring-opening reaction of piperonyl ethylamine. Piperethylamine and phenol are added to a reaction vessel and cooled down. Hydrochloric acid is slowly added while heating up the mixture to 110°C, and refluxed for 12-44 hours until the reaction reaches completion. The solution is then slightly cooled and water is added, and the mixture is stirred well and allowed to separate into layers. The upper phenolic layer is then removed, and the aqueous layer is extracted with isopropyl acetate. The extracted aqueous layer is then evaporated under reduced pressure (8.0kPa) until dry. Half the amount of ethanol and hydrochloric acid are added to the dry residue and heated to dissolve. The solution is then cooled, crystallized, and filtered. The filter cake is washed with ethanol and dried to obtain the final product, with a yield of 74%.

Показания

Dopamine HCl is indicated for the correction of hemodynamic imbalances present in the shock syndrome due to myocardial infarction, trauma, endotoxic septicemia, open-heart surgery, renal failure, and chronic cardiac decompensation as in congestive failure.

прикладной

Dopamine hydrochloride has been used to study dopamine-mediated transient modulation of the physiological responses in whiteleg shrimp, Litopenaeus vannamei.
It has been used to study dopamine-mediated changes in immunity susceptibility to Lactococcus garvieae in the freshwater giant prawn, Macrobrachium rosenbergii.
It has been used to study the molecular link between dopamine-induced oxidative stress and mHtt (mutant Huntingtin) toxicity in relation to the activation of the autophagy pathway in an 'in vitro' model of parkinsonian Huntington's Disease.

Общее описание

Dopamine Hydrochloride is the hydrochloride salt form of dopamine, a monoamine compound with positive inotropic activity. Dopamine is a neurotransmitter which is a naturally occurring catecholamine. Dopamine hydrochloride salt is indicated as a medicine for the treatment of acute congestive and renal failures.

Биологическая активность

Endogenous neurotransmitter that acts as an agonist at dopamine D 1-5 receptors. Synthesized in the substantia nigra and ventral tegmental area, and is a precursor in noradrenalin and adrenalin biosynthesis.

Фармакокине?тика

Dopamine hydrochloride(62-31-7) is a precursor for the synthesis of epinephrine in the body. It has β (mainly β1 receptor) receptor agonism and α receptor agonism, and can also promote the release of norepinephrine. It can enhance myocardial contractility, increase cardiac output, and accelerate the heart rate to a lesser extent (not as obvious as isoproterenol); stimulate the α-receptors of blood vessels in tissues such as skin and muscles, so that blood vessels constrict and blood supply is reduced; it stimulates visceral blood vessels ( The dopamine receptors in the kidney, mesentery, and heart) dilate and increase blood flow. The change of total peripheral resistance is not obvious, but it is beneficial to improve the blood supply of vital organs during shock.

3-гидрокситирамин гидрохлорид препаратная продукция и сырье

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3-гидрокситирамин гидрохлорид поставщик

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