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Farmacêuticos Ativos

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Cyproheptadine Hydrochloride

Nº CAS. : 969-33-5

Fórmula Molecular: C21H22ClN

Peso molecular: 323.86

EINECS NÃO: 213-535-1

Cyproheptadine hydrochloride, also known as dibenzocycloheptadine, antigentadine, is a hexahydropyridine antihistamine, which can compete with histamine released from tissues for H1 receptors on effector cells, thus preventing the onset of allergic reactions and relieving the spasmogenic and congestive effects of histamine, which has a strong H1 receptor antagonistic effect and stronger antihistamine effect than paracetamol and promethazine. It has mild to moderate anti-5-hydroxytryptamine effect and anticholinergic effect.

Além disso, Cyproheptadine hydrochloride also has the effect of stimulating appetite, and weight gain can be seen after taking for a certain period of time.

Cyproheptadine hydrochloride is a white or yellowish crystalline powder, almost odorless, with a slightly bitter taste. It is soluble in methanol, dissolved in chloroform, slightly soluble in ethanol, slightly soluble in water and almost insoluble in ether.

Clinically, cyproheptadine hydrochloride is mainly used for acute and chronic urticaria (especially cold urticaria has good effect), papular urticaria, angioedema, allergic eczema, contact dermatitis, food allergic reaction, drug allergic reaction, allergic rhinitis, hay fever, allergic nodular inflammation, insect sting allergy and migraine.

Cyproheptadine hydrochloride has some therapeutic effect on bronchial asthma. It can also be used as an adjuvant treatment for Cushing's syndrome and acromegaly.

Cyproheptadine hydrochloride can also be used as an appetite enhancer for neurotic appetite fear.

Cyproheptadine hydrochloride has also been reported for the treatment of acanthosis nigricans and the prevention of necrotizing pyoderma.

ITEMS OF ANALYSIS SPECIFICATIONS RESULTADO
Aparência White to slightly yellow, odorless or

practically odorless, pó cristalino.

Pó Cristalino Branco
Identificação E:The infrared absorption spectrum of the potassium bromide dispersion of the sample exhibits maxima only at the same wavelengths as that of a similar preparation of Cyproheptadine Hydrochloride reference standard Cumpre
HPLC:The retention time of the cyproheptadine peak of the sample solution corresponds to that of the standard solution, as obtained in the test for organic impurities Cumpre
A saturated solution gives reaction of chlorides Cumpre
Solubilidade Freely soluble in methanol, sparingly soluble in chloroform, sparingly soluble in alcohol, slightly soluble in water practically insoluble in ether. Cumpre
Fluorescence Test To comply Cumpre
Residue of Ignition ≤ 0.1% 0.07%
Cinza Sulfatada ≤ 0.1% 0.08%
Light-absorbing impurities At 490nm ≤ 0.07 0.04
Organic Impurities by HPLC Cyproheptadine related compound C: ≤ 0.15% Não detectado
Amitriptyline related compound B ≤ 0.15% Não detectado
Cyproheptadine related compound A ≤ 0.15% 0.05%
Any individual unknown Impurity ≤ 0.1% 0.05%
Total impurities ≤0.5% 0.13%
Acidity

NMT 0.15 ml of 0.01 M sodium Hydroxide is

required to change the co lour of the indicator

0.1ml
Water Determination 7.0% para 9.0% 8.5%
Solventes Residuais Methanol ≤300ppm 163ppm
O-rylene ≤2170ppm Não detectado
lsopropyl alcohol ≤5000ppm 24ppm
Toluene ≤890ppm Não detectado
Tetrahydrofuran ≤720ppm Não detectado
Chloroform ≤60ppm Não detectado
Ensaio (Dry based) 98.5%~100.5% 100.2%
Conclusão Complies with the USP40 standard

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