Anti Stroke Powder Cp2015 99% Citicoline Sodium

• CAS No.: 33818-15-4
• Formula: 33818-15-4
• EINECS: 33818-15-4
• Grade: Pharm
• Function: Pharm
• Certification: MSDS, GMP, Halal
• Model NO.: Citicoline Sodium
• Usage: Pharm
• Raw Material: 33818-15-4
• Transport Machine: Ordinary Goods Truck
• Appearance: White Powder
• Transport Package: Drum
• Specification: 99%
• Trademark: Recedar
• Origin: China
• HS Code: 1302
• Production Capacity: 1000t

Product Description

CP2015 99% Citicoline Sodium powder with CAS 33818-15-4

Citicoline sodium
CAS: 33818-15-4
MF: C14H25N4NaO11P2
MW: 510.31
EINECS: 251-689-1
Chemical Properties White Solid
Usage Naturally occurring nucleotide; intermediate in the major pathway of lecitin biosynthesis. Neuroprotective. It is used in the treatment of ischemic stroke and head trauma.

Citicoline sodium can gradually restore the function of the limbs to hemiplegia caused by stroke, and can also be used for other functions and consciousness disorders caused by acute injury of the central nervous system, as well as for ischemic cerebrovascular disease and vascular dementia.

CP2015 99% Citicoline Sodium powder with CAS 33818-15-4

 

Package	carton drum with two plastic bags inside
Net weight	25KG/Drum
Storage	Sealed in cool and dry place to avoid moisture and light
Shelf life	2 years when properly stored
Lead time	1~3 days after confirmation

 anti stroke powder Cp2015 99% Citicoline Sodium

Test Items	Test Specifications
Appearance	White crystals or crystalline powder, odor
Solubility	Freely soluble in water, insoluble in ethanol and aceton
Identification	The color of solution reaction is positive
	In the assay, the retention time of the principle peak in the chromatogram obtained with the test solution is identical with that of the principle peak in the chromatogram obtained with the reference solution.
	The infrared absorption spectrum is concordant with the reference spectrum (IR album No.1096)
	The aqueous solution yields the reaction characteristic of sodium salts.
PH	6.0-7.5
Clarity and color of solution	Should be clear and colorless
Chlorides	≤0.05%
Ammonium	≤0.05%
Iron	≤0.01%
Phosphate	≤0.1%
Heavy metals	≤5ppm
As	≤0.0001%
Related substance
5'CMP	≤0.3%
Other single impurity	≤0.2%
Other total impurities	≤0.7%
Residual solvents
Metha nol	≤0.3%
Ethanol	≤0.5%
Aceton e	≤0.5%
Loss on drying	≤6.0%
Bacterial endotoxins	<0.30 EU/mg
Assay (on dried basis)	≥98.0% (C14H25N4NaO11P2)
Conclusion	Complies to the standard of ChP 2015 Part II.

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