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White Willow Bark Extract Powder

White Willow Bark Extract Powder

Part of Plant Used: Bark
Appearance:Brown to White Powder
Specification:Salicin 15%,20%,50%,95%
Testing Method: HPLC
Extract Method: Grain Alcohol/Water
CAS NO.: 138-52-3
Two Factories & Three production lines
GMP standard workshop & two independent laboratories
FDA Cert.
Certifications: Halal,ISO9001,PAHS Free,NON-GMO,KOSHER,SC
Overseas warehouse(NJ,USA)
Delivery term: DHL, FEDEX, Air freight,Sea freight
Provide Free Sample
MOQ: 1KG
Not for Private Person Sale

Description

White Willow Bark Extract Powder Supplier:

Guanjie Biotech specializes in white willow bark extract research and trading for 20 years. It is from the bark, branches, and stems of the Salicaceae plant, white willow, after extraction and spray drying. The main active ingredient is salicin, which is a brown to white powder. We have different specifications:15%,20%,50%,95% and use grain alcohol or the water extraction method. In order to ensure the quality, we use HPLC and other testing methods. As a professional supplier, welcome to enquiry us.

white willow bark bulk extract

Why Choose Guanjie Biotech?

● We have a warehouse in NJ, USA;

● Multiple shipping methods for your choice: FEDEX, DHL, TNT, UPS, SHIPMENT BY AIR &SEA;

● Competitive shipping price and experienced professional shipping agent;

● Customize Willow Bark Extract Powder Salicin products according to your requirements;

● Available Certificates of ISO9001, ISO22000, Kosher, Halal;

● Practical Base for Master's Students in the School of Chemistry and Materials Science, Northwest University.

 

What Is White Willow Bark Extract Powder?

White Willow Bark Extract Powder Salicin is a white crystal with a bitter taste and a melting point of 199-202℃. Its specific optical rotation [α] is -45.6° (0.6g/100cm3 absolute ethanol). Salicin is soluble in water, easily soluble in boiling water, insoluble in ethanol (1:90), and insoluble in ether or chloroform. However, it is soluble in alkaline solution, pyridine or glacial acetic acid. Its aqueous solution has a neutral reaction, and the molecule does not contain a free phenolic hydroxyl group, making it a phenolic glycoside compound. When hydrolyzed by dilute acid or amygdalin, it generates glucose and salicyl alcohol. Salicyl alcohol has a molecular formula of C7H8O2, and it is an orthorhombic colorless needle crystal with a melting point of 86-87°C. When heated to 100°C, it sublimes and is soluble in water and benzene. Salicyl alcohol is easily soluble in ethanol, ether, and chloroform and turns red when it meets sulfuric acid.

 

COA

 Item

Specification

Result

Method

Marker Compounds

     

Assay (Salicin)

>15.0%

>15.12%

HPLC

Organoleptic Data

     

Appearance

Fine Powder

Conform

GJ-QCS-1008

Color

Light yellow

Conform

GB/T 5492-2008

Odor

Characteristic

Conform

GB/T 5492-2008

Taste

Characteristic

Conform

GB/T 5492-2008

Process Data

     

Method of Processing

Extraction

Conform

/

Solvent(s) Used

Ethanol&Water

Conform

/

Drying Method

Spray drying

Conform

/

Physical Characteristics

     

Particle Size (80 mesh)

98.0%pass 80mesh

Conform

GB/T 5507-2008

Loss on drying

<5.0%

3.03%

GB/T 14769-1993

Ash Content

<4.0%

2.15%

AOAC 942.05, 18th

Solvent Residue

None

Conform

GJ-QCS-1007

Sterilization Method

NO-IR & GMO-Free

Conform

/

Heavy Metals

     

Total Heavy Metals

<10ppm

Conform

USP <231>, method II

As

<2.0ppm

Conform

AOAC 986.15, 18th

Pb

<2.0ppm

Conform

AOAC 986.15, 18th

Cd

<0.5ppm

Conform

AOAC 986.15, 18th

Hg

<0.5ppm

Conform

AOAC 971.21, 18th

Cr

<2.0ppm

Conform

AOAC 986.15, 18th

Pesticide Residue

     

666

<0.2ppm

Conform

GB/T5009.19-1996

DDT

<0.2ppm

Conform

GB/T5009.19-1996

Microbiology

     

Total Plate Count

<1,000/g

90/g

AOAC 990.12, 18th

Total Yeast & Mold

<100/g

10/g

FDA (BAM) Chapter 18, 8th Ed.

E. Coli

Negative

Negative

AOAC 997.11, 18th

Salmonella

Negative

Negative

FDA (BAM) Chapter 5, 8th Ed.

Shigella

Negative

Negative

AOAC 997.11, 18th

Clostridia

Negative

Negative

FDA (BAM) Chapter 5, 8th Ed.

 

Specification:

There are different specifications of white willow bark extract powder. 

● 15% brownish yellow, high ash content, general water solubility

● 25% brownish yellow, high ash content, general water solubility

● 30% yellow, high ash content, good water solubility

● 50% light yellow, high ash content, good water solubility

● 80% off-white, low ash content, good water solubility

● 98% white, low ash, good water solubility

 

What Is White Willow Bark Extract Powder Produced?

Salicin flow chart

 

What Is the Testing Method of White Willow Bark Extract Powder?

The quality and standardization of white willow bark extract powder are primarily evaluated by determining the content of salicin, the key bioactive compound responsible for its functional properties. High-performance liquid chromatography (HPLC) is commonly used due to its accuracy, sensitivity, and reproducibility in quantitative analysis.

 

Testing Method - Detection of White Willow Bark Extract Powder Salicin

Note: All solvents used in the analysis should be chromatographic grade to ensure precision and avoid interference during detection.

Chromatographic Conditions

The analysis is carried out using a Lichrospher C18 chromatographic column (250 mm × 4.6 mm, 5 μm particle size). The mobile phase consists of acetonitrile and water at a ratio of 10:100. The flow rate is maintained at 1.0 mL/min to achieve optimal separation efficiency. Detection is performed at a wavelength of 269 nm, which corresponds to the maximum absorption of salicin. The column temperature is controlled at 30 °C to ensure stable retention time and peak shape, while the injection volume is set at 10 μL.

 

Solution Preparation

● Reference Solution Preparation: Accurately weigh 20 mg of the White Willow Bark Extract Powder salicin reference standard and transfer it into a 50 mL volumetric flask. Add purified water to dissolve completely and dilute to volume to obtain the standard solution.

● Sample Solution Preparation: Precisely weigh 15 mg of the white willow bark extract powder into a 25 mL volumetric flask. Add water and subject the mixture to ultrasonic extraction for 20 minutes to ensure complete dissolution. After cooling, dilute to volume with water and filter through a 0.45 μm microporous membrane before analysis.

 

Determination

Once the chromatographic system reaches a stable baseline, inject the prepared sample solution under the specified conditions. The White Willow Bark Extract Powder Salicin content is quantified using the external standard method by comparing the peak area of the sample with that of the reference standard. This method ensures reliable quality control and consistent product standardization.

 

Factory&Team:

Factory&Team

 

Certification

Certification

 

Package & Shipment

Package & Shipment

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