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Email ：PharmaSources@imsinoexpo.com
Whatsapp ：+86-13621645194
Main Sales Markets: North America,Central/South America,Western Europe,Eastern Europe,Australasia,Asia,Middle East,Africa
Monthly Production Capacity: 500kg/month
Packaging Information: Single aluminum can package
Delivery Lead Time: 5 days after receiving purchase order
Sample Provided: yes
Payment Terms: L/C D/A D/P T/T
Source: Bovine (Porcine) pancreas
General description
Chymotrypsin (chymotrypsin), endopeptidase. White or light yellow crystalline or amorphous powder, soluble in water, insoluble in organic solvents. When applied to protein, selective hydrolysis L - tyrosine and the carboxyl group of L - phenylalanine peptide bond formation.
Manufacture
Trypsin production of Beijing Geyuantianrun Bio - tech Co., ltd. is by protein chromatography technology preparation, reach the standard pharmaceutical raw materials..
Application
As pharmaceutical raw materials manufacturing injection. it always used to general trauma, wound healing that after surgery, anti-inflammatory, prevent local edema, hematocele, sprain hematoma, partial swelling that after breast surgery, tympanitis, rhinitis and so on. Use for the removal of cataract, Loose the lashes muscle ligament, reduce the cyst rupture and the hurt of retina.Besides, the combination use with the Trypsin and used as a broad-spectrum anti-inflammatory drugs.
As an aid in the medication of antibiotics and antibacterial drug, widely used in the field of animal medicine and animal health..
Specification
Items
Specification
Standard
Appearance
White or almost white lyophilized powder
USP37
Identification
No purple color develops within 3 minutes
USP37
Loss on drying
No more than 5.0%
USP37
Residue on Ignition
No more than 2.5%
USP37
Microbial limits:
Pseudomonas aeruginosa
Salmonella
Staphylococcus aureus
Absent
USP37
Trypsin
No more than 1%
USP37
Assay
Chymotrypsin≥1000 USP units/mg powder
USP37
Items
Specification
Standard
Description
White crystalline lyophilized powder
EP8.0
Identification
A) A purple colour develops
B)No purple colour develops within 3 min of mixing
EP8.0
Appearance of solution
Solution S is not more opalescent than
reference suspension Ⅱ
EP8.0
Absorbance
1) 281nm : 18.5 ~ 22.5
2) 250nm : not more than 8.0
EP8.0
PH
3.0-5.0
EP8.0
Histamine
Not more than 1µg/5.0µkatal
EP8.0
Loss on drying
Not more than 5%
EP8.0
Limit of trypsin
Not more than 1%
EP8.0
Microbial limits:
Pseudomonas aeruginosa
Salmonella
Absent
EP8.0
Assay
Not less than 5.0 ukatal/mg, calculated on the dried basis
Twelve years of qualification
Audited Supplier
Pharma Sources Insight JANUARY 2024
