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  Nivaliln (Galantamine)
 Nivalin introduction
 Nivalin (Galantamine) is the result of a natural product
 Nivalin (Galantamine) and the adrenals
 Nivalin pharmacokinetics
 Safety and Toxicity studies
 Mutagenicity of Nivalin (Galantamine)
 Clinical application of Nivalin
 References
 Table of Contents
 Galantamine HBr
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Nivalin (Galantamine) is an original phytopreparation developed by Sopharma's own research team and produced with an original technology for extraction of the alkaloid Galantamine from the bulbs of the plant snowdrops (Leucojum aestivum).
 
 
 
 
 DOGtor Rx for Frail Geriatric Dogs, Cushinoid and Cushing, Dog Joint and Ligament Pains, Dog Separation Anxiety, Pet Skin Hot Spots, Pet Fur Shedding
DOGtor Rx for Frail Geriatric Dogs
Bulgarian Rose Co.
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Galantamine HBr substance  
 

Item # 103-09

DESCRIPTION: The product is an alkaloid extracted from the tuberous plant Leucojum aestivum L. from the Amaryllidaceae family. It is manufactured as galanthamine hydrobromide. Galanthamine bromide substance is used in the manufacturing of the medication Nivalin, which is a strong (reversible) cholinesterase inhibitor, increasing the susceptibility of the organism to acetylcholine.

It facilitates the transmission of impulses in neuromuscular synapses and restores neuromuscular transmission. The drug crosses the hematoencephalic barrier and in proper doses facilitates the transmission in the synapses of the central nervous system, and enhances the excitation processes. It enhances the tone of the smooth muscles and intensifies the secretion of the gastric and sweat glands.

MOLECULAR MASS: 368.28 (hydrobromide) and 287.36 (base)

PHYSICO-CHEMICAL INDICES OF THE FINISHED PRODUCT

 
¤ AppearanceFine crystalline powder
¤ ColorWhite or almost white
¤ OdorNone
¤ Solubility 

in water

Poorly soluble

in 95% alcohol

Practically insoluble

in chloroform

Practically insoluble

in ether

Practically insoluble
¤ Specific rotation [α] 20D solution with concentration of 2.0 g/100 ml (°)From -90.0 to -100.0
¤ Sulphates content (mg/g)Not more than 1.0
¤ Sulphate ash (%)Not more than 1.0
¤ Heavy metal content (mg/g)Not more than 20.0
¤ Weight loss on drying (mg/g)Not more than 10.0
¤ Galanthamine bromide content (%) 

Calculated as dry substance

98.0 - 100.5
¤ Microbial content 

Total microorganisms (number/g)

Not more than 10 -3

Moulds and yeast (number/g)

Not more than 10 -2

Enterobacteriaceae, Ps. Aeruginosa, St. aureus

Not allowed

SUPPLIED: The substance is filled in polyethylene bags of 2 kg and placed in cardboard barrels.

QUALITY: Bulgarian State Standard

EXPIRY: 5 YEARS

MEDICINAL FORM AND PACKAGE:

NIVALIN original Bulgarian patented medicine

  • Ampoules of 1 mg/ml; 2.5 mg/ml; 5 mg/ml and 10 mg/ml in packs of 10, 50 and 100
  • Syrup of o.5 mg/ml in bottles of 125 ml
  • Tablets of 1 mg and 5 mg in packs of 50 and 10 mg in packs of 20.
 
 
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