Factory Supply High Quality Acetaminophen CAS#103-90-2

• Customization: Available
• Powder: Yes
• Customized: Customized
• Model NO.: Frazer-Acetaminophen
• Suitable for: Elderly, Children, Adult
• Purity: >99%
• Assay: 90% Min Paracetamol
• Test: HPLC
• Storage: Cool Dry Place
• MW: 240.75
• Grade Standard: Medicine Grade
• Shelf Life: 2 Years Proper Storage
• Active Ingredient: Paracetamol
• Case No: 103-90-2
• Sample: Paracetamol Avaliable
• Package: 1kg Per Foil Bag, 10 Bags Per Carton. 25 Kg Per Dr
• Appearance: White Powder
• Color: White
• Certificate: GMP ISO USP Bp
• Transport Package: Foil Bag
• Specification: 99%
• Trademark: Xi′an Frazer Biotech Co., Ltd.
• Origin: China
• Production Capacity: 1000kg/Month

Product Description

Factory Supply High Quality Acetaminophen CAS#103-90-2

Basic detials:

Product Name	Paracetamol bp
Appearance	White or white crystalline powder
Assay	99%min
Test	HPLC
Certificate	ISO 9001
CAS	103-90-2
MF	C17H19N3O3S
Einecs No	137-58-6
Dosage Form	Powder
Storage Temperature	Keep in a cool, dry, dark location in a tightly sealed container or cylinder.
Shelf Life	24 Months

 

What is Paracetamol? 

Paracetamol:
Mainly used for amino acid infusion,due to special wettability, also used in cold cream,osmetics. Serine constitute the human body of several kinds of essential amino acid of protein a, for the construction of protein has a very important role. 

The antipyretic and analgesic acetaminophen, this product is a metabolite of , regulates central prostaglandin synthase by inhibiting hypothalamic body temperature. Reduce the synthesis and release of prostaglandin PGE1, bradykinin and histamine. PGE1 mainly acts on the nerve center.


Purpose:

1. Paracetamol is the most commonly used non-inflammatory antipyretic analgesic. Its antipyretic effect is similar, its analgesic effect is weak, and it has no anti-inflammatory and anti rheumatic effect.

2. Paracetamol is used as antipyretic, analgesic and anti rheumatic drugs

3. Paracetamol is used in organic synthesis intermediates, photographic chemicals and non anti-inflammatory, antipyretic and analgesic drugs.


Usage Method:

1. Oral administration of
(1) paracetamol tablets and capsules: 300 ~ 600mg for adults once, 3 ~ 4 times a day as required, and the daily dosage should not be > 2G. Antipyretic treatment generally does not exceed 3 days, and analgesic administration does not exceed 10 days. Children take 10 ~ 15mg / kg once every 4 ~ 6h; The dose of small chemicalbook infants under 12 years old shall not exceed 5 times a day, and the course of treatment shall not exceed 5 days. This product is not suitable for long-term use.

2. Dispersible tablets: when taking, heat boiled water to disperse. The commonly used dose for children is 10 ~ 15mg / kg once, once every 4 ~ 6h. The dose for children under 12 years old shall not exceed 5 times a day, and the course of treatment shall not exceed 5 days. The dose for children under 3 years old shall be reduced as appropriate.

COA

Tests	Standards	Results
Appearance	White or almost white ,crystalline powder.	White,crystalline powder.
Identification	A:IR absorption	Complies
	B:UV absorption	Complies
	C:TLC	Complies
Melting point	168~172°C	169.0~170.9°C
Water	Not more than0.5%	0.08%
Related substance	ImpurityJ(chloroacetanilide)not more than 10 ppm	2ppm
	Impurity K(4-aminophenolly)not more than 50 ppm	15 ppm
	Impurity F(4-nitrophenolly)not more than 0.05%	Not detected
	any other impurity not more than 0.05%	0.01%
	Total of other impurities not more than 0.1%	0.02%
Residue on ignition	Not more than 0.1%	0.05%
Chloride	Not more than 0.014%	Less than 0.014%
Sulfate	Not more than 0.02%	Less than 0.02%
Sulfide	Conforms	Conforms
Heavy metals	Not more than 0.001%	Less than 0.001%
Free p-aminophenol	Not more than 0.005%	Less than 0.005%
Limit of P-chloroacetanilide	Not more than 0.001%	Less than 0.001%
Readily carbonizable substances	Conforms	Conforms
Residual solvents	Residual content of acetic acid is limited by the test of loss on dryingnot more than0.5%	0.08%
Assay(anhydrous basis)	99.0~101.0%	99.6%
Conclusion:   Complies with USP34/ BP2011