Product Details
Place of Origin: China
Brand Name: BBCA
Certification: GMP
Payment & Shipping Terms
Minimum Order Quantity: 1000 kgs
Price: Negotiated
Packaging Details: 25 kgs/bag/drum
Delivery Time: 7-15 working days after payment normally
Payment Terms: L/C, T/T
Supply Ability: 10000 mts per year
Characters: |
White ，crystalline Powder |
CAS No:: |
103-90-2 |
Grade Standard:: |
Medicine Grade |
Brand Name:: |
BBCA |
Characters: |
White ，crystalline Powder |
CAS No:: |
103-90-2 |
Grade Standard:: |
Medicine Grade |
Brand Name:: |
BBCA |
BBCA Active Pharmaceutical Ingredient Paracetamol Powder CAS No 103-90-2
Active Pharmaceutical Ingredient Paracetamol Powder
Introduction
CAS No.:103-90-2
Molecular Formula: C8H9NO2
Molecular Weight: 151.16
EINECS: 203-157-5
Purity: 98.0%~102.0%
Certificate of Analysis, BP/EP/USP
Appearance: A white to pale yellow crystalline powder. Odorless and a little bitter.
Function
Paracetamol powder nutritional supplement Mainly used for amino acid infusion,due to special wettability, also used in cold cream,cosmetics. 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.
Application
Paracetamol powder nutritional supplemen 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.
Specification
| Contents | Specification | Results | ||
| Characters | White ,crystalline powder | Conforms | ||
|
Identification |
A:IR absorption | Conforms | Conforms | |
|
B:The retention time of the major peak of the Sample solution corresponds to that of the standard solution,as obtained in the assay. |
Conforms |
Conforms |
||
| Loss on drying | ≤0.5% | 0.08% | ||
| Residue on ignition | ≤0.1% | 0.07% | ||
| Free p-aminophenol | ≤0.005% | 0.0002% | ||
|
Related substances |
Impurity B | ≤0.05% | Below LOD | |
| Impurity C | ≤0.05% | Below LOD | ||
| Impurity D | ≤0.05% | Below LOD | ||
| Impurity J | ≤0.001% | Below LOD | ||
| Individual unspecified impurity | ≤0.05% | 0.02% | ||
| Total of impurities | ≤0.1% | 0.03% | ||
| Residual solvents | Residual content of acetic acid is limited by the test of loss on drying. | ≤0.5% | 0.07% | |
| Organic volatile impurities | Conforms | Conforms | ||
| Assay(anhydrous basis) | 98.0%-102.0% | 99.6% | ||
| Conclusion: It complies with the requirements of the USP42 | ||||
