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4-Аминосалициловая кислота

4-Аминосалициловая кислота структура
65-49-6
CAS №
65-49-6
Химическое название:
4-Аминосалициловая кислота
английское имя:
4-Aminosalicylic acid
Синонимы:
4-AMINO-2-HYDROXYBENZOIC ACID;PAS;AMINOSALICYLIC ACID;Pasa;4-Asa;P-AMINOSALICYLIC ACID;Apas;Paser;Aminox;Parasal
CBNumber:
CB9679687
Формула:
C7H7NO3
молекулярный вес:
153.14
MOL File:
65-49-6.mol

4-Аминосалициловая кислота атрибут

Температура плавления: 135-145 °C (lit.)
Температура кипения: 276.03°C (rough estimate)
плотность: 1.3585 (rough estimate)
показатель преломления: 1.5500 (estimate)
температура хранения: Keep in dark place,Inert atmosphere,Room temperature
растворимость: 1,69 г/л
форма: пудра
пка: 3.25(at 25℃)
цвет: Бесцветный и прозрачный
РН: 3.5 (1g/l, H2O, 20℃)
Растворимость в воде: 2 g/L (20 ºC)
Мерк: 14,477
БРН: 473071
BCS Class: 4/2
Стабильность:: гигроскопичный
Справочник по базе данных CAS: 65-49-6(CAS DataBase Reference)
Рейтинг продуктов питания EWG: 1
FDA UNII: 5B2658E0N2
Код УВД: J04AA01
Справочник по химии NIST: Aminosalicylic acid(65-49-6)
Система регистрации веществ EPA: 4-Aminosalicylic acid (65-49-6)
безопасность
  • Заявления о рисках и безопасности
  • код информации об опасности(GHS)
Коды опасности Xn,Xi,T
Заявления о рисках 22-36-36/37/38-45-35-61
Заявления о безопасности 26-37/39-45-53-36-36/37/39
РИДАДР UN 1789 8/PG 3
WGK Германия 2
RTECS VO1225000
TSCA Yes
кода HS 29225000
Банк данных об опасных веществах 65-49-6(Hazardous Substances Data)
Токсичность LD50 orally in mice: 4 g/kg (Bavin)
символ(GHS) GHS hazard pictograms
сигнальное слово Warning
Заявление об опасности
пароль Заявление об опасности Класс опасности категория сигнальное слово пиктограмма предупреждение
H315 При попадании на кожу вызывает раздражение. Разъедание/раздражение кожи Категория 2 Предупреждение GHS hazard pictograms P264, P280, P302+P352, P321,P332+P313, P362
H319 При попадании в глаза вызывает выраженное раздражение. Серьезное повреждение/раздражение глаз Категория 2А Предупреждение GHS hazard pictograms P264, P280, P305+P351+P338,P337+P313P
H335 Может вызывать раздражение верхних дыхательных путей. Специфическая токсичность на орган-мишень, однократное воздействие; Раздражение дыхательных путей Категория 3 Предупреждение GHS hazard pictograms
Внимание
P261 Избегать вдыхания пыли/ дыма/ газа/ тумана/ паров/ аэрозолей.
P264 После работы тщательно вымыть кожу.
P280 Использовать перчатки/ средства защиты глаз/ лица.
P304+P340 ПРИ ВДЫХАНИИ: Свежий воздух, покой.
P405 Хранить в недоступном для посторонних месте.

4-Аминосалициловая кислота MSDS


PAS

4-Аминосалициловая кислота химические свойства, назначение, производство

Химические свойства

beige powder

Использование

antimycobacterial antitubercular;NF-kB inhibitor.
4-Aminosalicylic acid (p-aminosalicylic acid, PAS), an antituberculosis drug, is a model active pharmaceutical ingredient to study salt and cocrystal formation in a multiple hydrogen-bonding functionality molecule with carboxylic acid, amine, and phenol groups.
It has also been used as a second line agent to sulfasalazine in people with inflammatory bowel disease such as ulcerative colitis and Crohn's disease.It is typically taken by mouth.

прикладной

4-Aminosalicylic acid (4-ASA) can be used in the synthesis of:
Azo derivatives of 4-ASA with anti-inflammatory effects.
Ammonium 4-aminosalicylate salt polymorphs which are used as pharmaceutical ingredients.
Salicylic acid-triazole analogs which are used as quorum sensing inhibitors against Pseudomonas aeruginosa.

Показания

p-Aminosalicylic acid is a bacteriostatic that inhibits most tuberculous mycobacteria. In terms of tuberculostatic activity it is inferior to isoniazid and streptomycin. It is nephroand hepatotoxic, and is rarely used. A synonym of this drug is apacizin.

Определение

ChEBI: An aminobenzoic acid that is salicylic acid substituted by an amino group at position 4.

Общее описание

4-Aminosalicylic acid occurs as a white to yellowish white crystalline solid that darkens on exposure to light or air. It is slightly soluble in water but more soluble in alcohol. Alkali metal salts and the nitric acid salt are soluble in water, but the salts of hydrochloric acid and sulfuric acid are not. The acid undergoes decarboxylation when heated. An aqueous solution has a pH of approximately 3.2. PAS is administered orally in the form of the sodium salt, usually in tablet or capsule form. Symptoms of gastrointestinal irritation are common with both the acid and the sodium salt. Various enteric-coated dosage forms have been used in an attempt to overcome this disadvantage. Other forms that are claimed to improve gastrointestinal tolerance include the calcium salt, the phenyl ester, and a combination with an anion exchange resin (Rezi-PAS). An antacid such as aluminum hydroxide is frequently prescribed. The oral absorption of PAS is rapid and nearly complete, and it is widely distributed into most of the body fluids and tissues, with the exception of the CSF, in which levels are significantly lower.It is excreted primarily in the urine as both unchanged drug and metabolites.

Биологическая активность

4-Aminosalicylic acid is an antimetabolite of p-aminobenzoic acid (PABA) that has antibacterial activity.It is active against streptomycin-sensitive and -resistant strains of M. tuberculosis (MICs = 0.78 and 0.39 μg/ml, respectively), an effect that can be reversed by PABA. 4-Aminosalicylic acid is an alternative substrate for mycobacterial dihydropteroate synthase (FolP1) and misincorporation into the folate pathway leads to accumulation of several folate-dependent metabolites including serine, homocysteine, dUMP, and AICAR, markers of folate pathway inhibition, in a concentration-dependent manner. It reverses manganese-induced increases in rat hippocampal levels of NOD-like receptor protein 3 (NLRP3), cleaved caspase-1, and phosphorylated p65, markers of NLRP3 inflammasome-dependent pyroptosis, when administered at a dose of 300 mg/kg. 4-Aminosalycilic acid is also a building block that has been used in the synthesis of luminescent lanthanide complexes. Formulations containing 4-aminosalicylic acid have been used in the treatment of tuberculosis.

Механизм действия

p-aminosalicylic acid is thought to act as an antimetabolite interfering with the incorporation of p-aminobenzoic acid into folic acid. When coadministered with INH, PAS is found to reduce the acetylation of INH, itself being the substrate for acetylation, thus increasing the plasma levels of INH. This action may be especially valuable in patients who are rapid acetylators.

Профиль безопасности

Moderately toxic ingestion andother routes. An eye irritant. Mutation data reported.When heated to decomposition it emits toxic fumes ofNOx.

Метаболизм

p-aminosalicylic acid is extensively metabolized by acetylation of the amino group and by conjugation with glucuronic acid and glycine at the carboxyl group. It is used primarily in cases of resistance, retreatment, and intolerance of other agents and is available from the CDC.

Методы очистки

Crystallise the acid from EtOH. [Beilstein 14 IV 1967.]

4-Аминосалициловая кислота препаратная продукция и сырье

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4-Аминосалициловая кислота поставщик

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