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Chymotrypsinogen
单价 面议对比
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发货
过期 长期有效
更新 2025-08-14 12:25
 
详细信息

Grade: food grade, pharmaceutical grade, injection grade, veterinary use, etc.

Factory Location: China Beijing Beijing

Main Sales Markets: North America,Western Europe,Eastern Europe,Australasia,Asia,Middle East

Sample Provided: no

Payment Terms: TT 、LC

Source: Bovine (Porcine) pancreas

General description

Chymotryupsin is white and light yellow crystal or amorphous powder, and easily soluble in the water, but insoluble in organic solvent. Relative molecular mass is 24000, and the optimum PH is 8~9. It is stable at a dry state, but will be quickly deactivated in water solution, most stable in the water solution with PH3~4. When it acts on the protein, it will hydrolyze the peptide bond formed by the carboxyl of L-tyrosine and L-phenylalanine in priority.

The high purity Chymotrypsin of Beijing Geyuantianrun Bio-tech Co., Ltd.. is purified by re-crystallization, and then by Ion Exchange Chromatography and ultra-filtration.

Application

Ø  In the clinical, 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.

Ø  as the auxiliary medicine of antibiotic and antifungal drugs,it is widely used in  the field of animal medicine and animal health industry.

 

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

EP8.0

Storage

 Sealed, Dark, at temperature 2-8℃