Factory Price Natural Papaya Extract CAS 9001-73-4 Papaya Enzyme Papain Powder

• Customization: Available
• Certification: RoHS, BRC, ISO, FDA, HACCP
• Assay Method: HPLC-MS, GPC, HPLC, UV
• Model NO.: Papaya Extract
• Application Form: Injection, Lotion, Suppository, Paste, Tablet, Capsule
• Application: Food, Health Care Products, Medicine
• State: Powder
• Product Name: Resveratrol
• Grade: Food Grade
• Appearance: White Fine Powder
• Test Method: HPLC
• Solubility: Insoluble in Water
• MOQ: 1 Kg
• Sample: Free Sample
• Transport Package: Drum, Aluminum Foil Bag
• Specification: 98%
• Trademark: SENTIAN
• Origin: Shanxi, China
• Production Capacity: 50000tons/Year

Product Description

PRODUCT INFORMATION
CAS 9001-73-4 papain enzyme powder
Papain is a natural enzyme, a kind of endopeptidese containing hydrosulfide group (-SH), extracted from the milky juice of the unripe papaya by biotechnology. It has strong ability of hydrolyzing protein and can be used for improving the nutritional value or function of the plants and the animal protein.
 

Food industry
In the food industry, papain can be used for meat tenderization, beer clarification, and biscuits loosening.
Beer clarifier
The main reason that causes the turbidity of beer in cold storage is that the protein in beer is easily combined with polyphenols to form macromolecular complexes. The use of papain in beer clarifiers has a wide range of specificity for the formation of turbid proteins, which can degrade large-molecule proteins into small-molecule substances, and improve the solubility of protein and polyphenol complexes; on the other hand, papain is A protein with biological activity, which can form a stable state balance with polyphenols that cause beer cold storage turbidity, and prevents beer cold storage turbidity.

Product Parameters

RESVERATROL SPECIFICATION
Product Name	PAPAIN
Grade	Food Grade
Specification	98% 99%
Appearance	Fine Powder
Test Method	HPLC
Solubility	Insoluble In Water
CAS	501-36-0
MOQ	1 Kg
Sample	Free Sample

 

ANALYSIS	SPECIFICATION	RESULTS
Appearance	Fine powder	Complies
Odor	Characteristic	Complies
Tasted	Characteristic	Complies
Specification	98%	Complies
Sieve Analysis	100% pass 80 mesh	Complies
Loss on Drying	5% Max.	1.02%
Sulphated Ash	5% Max.	1.30%
Heavy Metal	5ppm Max	Complies
As	2ppm Max	Complies
Residual Solvents	0.05% Max.	Complies
Microbiology
Total Plate Count	1000/g Max	Complies
Yeast & Mold	100/g Max	Complies
E.Coli	Negative	Negative
Salmonella	Negative	Negative

INTRODUCTION TO PHARMACEUTICAL INTERMEDIATES

Pharmaceutical intermediates are critical components in the development and production of active pharmaceutical ingredients (APIs). These compounds, often complex, serve as the building blocks for various medications. The role of pharmaceutical intermediates cannot be overstated as they significantly affect the efficiency, quality, and cost-effectiveness of drug manufacturing.

ADVANTAGES OF PHARMACEUTICAL INTERMEDIATES

* Cost Efficiency: High-quality intermediates can reduce overall production costs by streamlining processes and minimizing waste.
* Quality Assurance: When sourced from reliable manufacturers, intermediates guarantee consistency and compliance with regulatory standards.
 

ADVANTAGES OF PHARMACEUTICAL INTERMEDIATES

* Enhanced Efficacy: The right intermediates help in developing drugs that demonstrate enhanced therapeutic effects and patient outcomes.
* Innovation Facilitation: Intermediates often serve as key components in innovative drug formulations, aiding in the exploration of new therapeutic avenues.

APPLICATIONS OF PHARMACEUTICAL INTERMEDIATES

* Active Pharmaceutical Ingredients (APIs): Intermediates are crucial in the synthesis of APIs, which are the biologically active components of medications.
* Research and Development: These intermediates are used in the laboratory for drug discovery, leading to the creation of novel therapeutic compounds.
 

APPLICATIONS OF PHARMACEUTICAL INTERMEDIATES

* Formulations: They are integral in developing formulations for solid, liquid, and injectable medications.
* Regulatory Compliance: Pharmaceutical intermediates must meet stringent regulatory standards, ensuring safety and efficacy in end products.

FAQ

Q1. What's the MOQ?
A: MOQ is the minimum sales quantity of the product. Because each product has different prices and different packaging methods, there will be differences. Please consult the relevant professional sales manager for details.

Q2. What's the shipping time?
A: Usually the products we sell have enough stock to deliver the goods in a short

Q3.What transportation methods does our company have?
A: Our company cooperates with DHL and FedEx, as well as airlines and shipping companies. There are also some more efficient transportation methods, such as dedicated transportation lines.

Q4. Can you supply the free sample?
A: Generally, we will provide samples for customer testing to ensure that the quality of our products meets customer requirements.

Q5.Does our company support third-party testing?
A: Our company has long-term cooperation with well-known third-party testing agencies and can provide third-party testing services.