Trypsin powder CAS ...

Trypsin powder CAS 9002-07-7 Parenzyme

Trypsin powder CAS 9002-07-7 Parenzyme

Min.Order / FOB Price:Get Latest Price

5 Kilogram

FOB Price: USD 108.0000

  • Min.Order :5 Kilogram
  • Purity: ≥98.0%
  • Payment Terms : T/T,Other

Keywords

Trypsin Parenzyme 9002-07-7

Quick Details

  • Appearance:white lyophilized powder
  • Application:Health and medicne
  • PackAge:5 kg/tin
  • ProductionCapacity:2000|Kilogram|Week
  • Storage:Cool, dry, dark in closed containers; recommended limit 2 years.
  • Transportation:deliver within 2-8 days

Superiority:

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Details:

【Item name】Trypsin
【Synonyms】Trypsin-EDTASolution1X;α-and-trypsin;Tryprar; Trypsevas;Trypsin powder
【CAS NO.】9002-07-7
【enzyme activity】≥2500USP.U/mg (dried basis)
【Appearance】White lyophilized powder 
【Standard】Medicine grade, Tech. grade

 

Trypsin is a kind of serine proteolytic enzyme, extracted from healthy porcine pancreas or bovine pancreas and further prepared by a special process. the characters is white or almost white crystal powder, odourless, hygroscopic. It is a single peptide chain composed of 223 amino acid residues. With rigorous specificity, the trypsin specifically acts on peptide linkage composed of the basic amino acid arginine and leucine. Enzyme easily autolyzes by itself, and its activation reduces or loses gradually. Trypsin is easily soluble in the water, but insoluble in trichloromethane, ethanol, etherand and glycerin.

Solubility: An amount, equivalent to 500000 USP Trypsin unit, is soluble in 10ml of water and in 10ml of saline.

Quality Standard

Item

Specifications   

Trypsin activity

2500 USP.U/mg

Appearance

White powder

Solubility

An amount, equivalent to 500000 USP Trypsin units, is soluble in 10ml of water and in 10ml of saline TS

Limit of Chymotrypsin

5.0%

Loss on Drying

≤5.0% at 60℃for 4 hours

Residue on Ignition

2.5%

Microbiological quality according to current USP Pharmacopoeia

Pseudomonas aeruginosa

Absence/g

Salmonella species

Absence/10g

Staphylococcus aureus

Absence/g

Packing 25kgs/drum (standard packing)

StorageIn an airtight container, avoid overheating.

Function

Cure part dropsy, haematoma, abscess and other diseases which caused by pus-chest, henothorax, surgical inflammation, canker, traumatic injuries. it also can be used to cure respiratory diseases by spray absorbance

Shanghai Soyoung Biotechnology Inc. a faithful and professional supplier and exporter of healthcare raw materials for pharmacy, nutrition and food industries for years with own laboratory and GMP standard factories.

Shanghai Soyoung has R&D Center and Testing Center, and has international advanced facilities of HPLC, GC, AAS, UV, TLC, LC-MS and IR equipments. 

Shanghai Soyoung has nearly 20 years production experience, it is producing in GMP workshop, each batch pass strict testing before shipment. Strict quality control is performed in every procedure from material sourcing, processing and testing to packing.

Company name

Shanghai Soyoung Biotechnology Inc.

Main Products

Health care ingredients

Location

Shanghai,China

Business Type

Manufacturer & Trader 

Year start exporting

2011

Number of employees

60-70 people

Factory area

18,000 square meters

Total annual sales volume

US$3,000,000-5,000,000

Main Markets

America,Europe,Mid East,Asia,South Africa and etc.

Certifications

GMP,ISO,HACCP,Kosher

Shanghai SOYOUNG onsite assessment conducted by Bureau Veritas commissioned at June 2018. Assessed Supplier of Shanghai SOYOUNG is a faithful and professional supplier of health raw materials in pharmacy, food, cosmetic and other fields for many years, with own laboratories and GMP standard factories.

1. 10+years specialized in health products field.
2. GMP/ISO certificated factories and stable supply chain.
3. Quality first, strictly control before shipments.
4. Custom synthesis by more than 20 professional chemists.
5. Small order,free sample and one step service available.
6. Rapid delivery, 1-6 business days from China warehouse.
7. Support 7 days refund money in case delay shipment.
8. Assessment conducted by Bureau Veritas at 2018.
 

 

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