Basic Info.
Model NO.
                                     Frazer-Acetaminophen
                                 Certification
                                     GMP, HSE, ISO 9001, USP, BP
                                 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 | ||