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Xinxiang Hongqi District Houyuan Chemical Co., Ltd.

Xinxiang Hongqi District Houyuan Chemical Co., Ltd.

Certified Store
Custom-Made
China Henan Xinxiang
HYJM@houyuanjm.com
+86-13333828291
0373-3695376

Catalog No. :

Pheniramine maleate

  • 132-20-7
  • 1kg
  • HYJM
  • 99.0%
  • China,Shanghai,Pudong
  • 3Day (s)
Packing :
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  • Product Details & Description

Product Info

Compound Pheniramine Maleate
CAS No. 132-20-7 Catalog No. Brand HYJM
Purity 99.0% Packing 1kg Grade
Lead Time 3Day (s) Origin Loading Port China,Shanghai,Pudong

PropertiesMore

Boiling Point 348.3ºC at 760 mmHg
Stability Stable. Incompatible with strong oxidizing agents.
Storage Condition Keep in a cool, dry, dark location in a tightly sealed container or cylinder. Keep away from incompatible materials, ignition sources and untrained individuals. Secure and label area. Protect containers/cylinders from physical damage.
Appearance & Physical State white powder
Water Solubility >=1 g/100 mL at 24 ºC
Flash Point 164.5ºC
Melting Point 104-108ºC
Vapor Pressure 5.07E-05mmHg at 25°C

Description

CAS:132-20-7

Product name:Pheniramine maleate

MF:C20H24N2O4

MW:356.42 

Melting Point:104-108°C

Density:1.2233 

Usage:Animal Pharmaceuticals

Purity:99.0%

Boiling Point:489.25°C

Appearance:White Powder


Product description

Pheniramine is an antihistamine with anticholinergic properties used to treat allergic conditions such as hay fever or urticaria. It has relatively strong sedative effects, and may sometimes be used off-label as an over-the-counter sleeping pill in a similar manner to other sedating antihistamines such as diphenhydramine. Pheniramine is also commonly found in eyedrops used for the treatment of allergic conjunctivitis.

Pheniramine is generally sold in combination with other medications, rather than as a stand-alone drug, although some formulations are available containing pheniramine by itself. As an example, Neo Citran contains pheniramine.

Derivatives of pheniramine include chlorphenamine, dexchlorpheniramine, dexbrompheniramine, dexchlorpheniramine, triprolidine, and brompheniramine. Two other halogenated derivatives, iodopheniramine and fluorpheniramine, are currently in use for research on combination therapies for malaria and some cancers. The halogenation of pheniramine increases its potency by 20-fold.

Pheniramine may cause drowsiness or bradycardia, and over-dosage may lead to sleep disorders. Overdose may lead to seizures, especially in combination with alcohol. People combining with cortisol in the long term should avoid pheniramine as it may cause lowered levels of adrenaline (epinephrine) which may lead to loss of consciousness.

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Pheniramine maleate

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132-20-7

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