Хлорфенирамин малеа
Хлорфенирамин малеа атрибут
| Температура плавления: |
130-135 °C (lit.) |
| альфа: |
-1～+1°(D/20℃)(c=5,DMF) |
| плотность: |
1.1984 (rough estimate) |
| показатель преломления: |
1.6800 (estimate) |
| Fp: |
9℃ |
| температура хранения: |
2-8°C |
| растворимость: |
Легко растворим в воде, растворим в этаноле (96%). |
| форма: |
Solid |
| цвет: |
От белого до почти белого |
| Запах: |
odorless |
| РН: |
4.0～5.5 (10g/l, 25℃) |
| Растворимость в воде: |
1-5 г/100 мл при 21 °C |
| Мерк: |
14,2180 |
| BCS Class: |
3/1 |
| ИнЧИКей: |
DBAKFASWICGISY-BTJKTKAUSA-N |
| LogP: |
3.389 (est) |
| FDA 21 CFR: |
310.545; 341.12 |
| FDA UNII: |
V1Q0O9OJ9Z |
| Код УВД: |
R06AB04,R06AB54 |
| Система регистрации веществ EPA: |
Chlorpheniramine maleate (113-92-8) |
| UNSPSC Code: |
41116107 |
| NACRES: |
NA.77 |
безопасность
- Заявления о рисках и безопасности
- код информации об опасности(GHS)
| Коды опасности |
T,F |
| Заявления о рисках |
25-39/23/24/25-23/24/25-11 |
| Заявления о безопасности |
36/37/39-45-36/37-16 |
| РИДАДР |
UN 2811 6.1/PG 3 |
| WGK Германия |
3 |
| RTECS |
US6504000 |
| TSCA |
Yes |
| Класс опасности |
6.1(b) |
| Группа упаковки |
III |
| кода HS |
29333990 |
| Токсичность |
LD50 orally in mice: 162 mg/kg (Smith) |
| символ（GHS） |
|
| 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 |
|
P264, P270, P301+P312, P330, P501 |
|
| Внимание |
| P301+P312+P330 |
ПРИ ПРОГЛАТЫВАНИИ: Обратиться за медицинской помощью
при плохом самочувствии. Прополоскать рот. |
|
Хлорфенирамин малеа химические свойства, назначение, производство
Описание
Chlorpheniramine is a histamine H1 receptor antagonist with an IC75 value of 0.0016 μg/ml for reversal of histamine-induced spasms in isolated guinea pig ileum. It protects against intravenous histamine-induced death (PD50 = 0.15 mg/kg) and delays induction of aerosolized histamine-induced coughing (ED100sec = 0.44 mg/kg) in guinea pigs. Chlorpheniramine (20 mg/kg, i.p.) prevents histamine-induced passive cutaneous anaphylaxis (PCA) in rabbits. It also reduces respiratory resistance and hypersecretion of tracheobronchial fluid in a dog model of histamine-induced asthma. Formulations containing chlorpheniramine have been used in the treatment of seasonal allergies.
Химические свойства
White Solid
Использование
(±)-Chlorpheniramine maleate salt has been used:
- as H1 receptor antagonist to determine the receptor function
- to block the effect of compound 48/80 on plasma IGF-I
- as a standard for fast sensing and determination by sequential injector coupled with potentiometer
Общее описание
Odorless white crystalline solid or white powder with a bitter taste. pH (2% aqueous solution) 5. pH (1% aqueous solution) 4-5.
Реакции воздуха и воды
Water soluble.
Профиль реактивности
A halogenated amine, ester. Amines are chemical bases. They neutralize acids to form salts plus water. These acid-base reactions are exothermic. The amount of heat that is evolved per mole of amine in a neutralization is largely independent of the strength of the amine as a base. Amines may be incompatible with isocyanates, halogenated organics, peroxides, phenols (acidic), epoxides, anhydrides, and acid halides. Flammable gaseous hydrogen is generated by amines in combination with strong reducing agents, such as hydrides. Esters react with acids to liberate heat along with alcohols and acids. Strong oxidizing acids may cause a vigorous reaction that is sufficiently exothermic to ignite the reaction products. Heat is also generated by the interaction of esters with caustic solutions. Flammable hydrogen is generated by mixing esters with alkali metals and hydrides.
Пожароопасность
Flash point data for Chlorpheniramine maleate are not available; however, Chlorpheniramine maleate is probably combustible.
Профиль безопасности
Poison by ingestion, intravenous, and subcutaneous routes. Experimental reproductive effects. Used as an antihistamine. Mutation data reported. When heated to decomposition it emits very toxic fumes of Cland NOx.
Хлорфенирамин малеа препаратная продукция и сырье
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Хлорфенирамин малеа поставщик
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