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Ranitidine Hydrochloride (Zantac) Powder Raw Digestive System Medication

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  • Specifications

Buy Ranitidine Hydrochloride  (Zantac) Powder Raw Digestive System Medication Online CAS 71130-06-8

 

Ranitidine Hydrochloride Specification

Product Name: Ranitidine Hydrochloride
CAS: 66357-59-3
Standard: USP
Content: 98%
Appearance: white powder
Packing: 25KG/cardboard drum
Ingredients: N’-Methyl-N-[2-[[[5-[(dimethylamino)methyl]-2-furyl]methyl]thio]ethyl]-2-nitro-1, 1-Ethylenediamine hydrochloride. Calculated on dry products, containing C13H22N4O3S · HCl should be 97.5% ~ 102.0%.
Physicochemical properties: white to pale yellow crystalline powder; odor; taste slightly bitter with astringent; easily deliquescent, the color becomes darker after absorbing moisture. This product is soluble in water or methanol, slightly soluble in ethanol, almost insoluble in acetone.
Category: Feed Additives
Field: Digestive system medication
Deferred Products: Compound Enteric Kang Drug
Application: Treatment of animal gastroenteritis with other drugs

 

What is Ranitidine?

Ranitidine, sold under the trade name Zantac among others, is a medication which decreases stomach acid production. It is commonly used in treatment of peptic ulcer disease, gastroesophageal reflux disease, and Zollinger–Ellison syndrome. There is also tentative evidence of benefit for hives.

Ranitidine can be taken by mouth, by injection into a muscle, or into a vein.

 

Ranitidine Hydrochloride Certificate of Analysis

Product name Ranitidine HCl
CAS No. 71130-06-8 Outer Packing 25KG/drum
Production date 2017.04.07 Shelf life 2019.04.06
Standard adopted USP36
Items of analysis Specification Results
Appearance, color White to light yellow crystalline powder; odor; taste bitter with astringent; easy deliquescence, moisture absorption after dark Conforms
Solubility Soluble in water, very slightly soluble in ethanol, almost insoluble in ether Conforms
Identification Whater liquor show chloride Conforms
Clarity and color Should Compliance Conforms
PH 4.5-6.0 5.4
impurity B ≤0.3% Conforms
Single impurity ≤0.1% Conforms
Total impurity ≤0.5% Conforms
Loss on drying ≤0.75% 0.25%
Residue on ignition ≤0.1% 0.06%
Heavy metal ≤20ppm Conforms
Assay 97.5-102% 99.72%
Conclusion Qualified

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