[Latin Name] Cinnamomun camphcra

[Plant Source] It is extracted from Ginkgo Biloba Leaf.

[Specifications]

1, Ginkgo Biloba Extract 24/6

Total Ginkgo flavone glycosides 24%

Total terpene lactones 6%

2, Ginkgo Biloba Extract 24/6

Total Ginkgo flavone glycosides 24%

Total terpene lactones 6%

Ginkgolic acid 5ppm

3,CP2005

Total Ginkgo flavone glycosides 24%

Quercatin: kaemperol 0.8–1.5

Total terpene lactones 6%

Ginkgolic acid <5ppm

4.Germany Standard

Total Ginkgo Flavone Glycosides 22.0%-27%

Total Terpene Lactones 5.0%-7.0%

Bilobalides 2.6%-3.2%

Ginkgolic acid <1ppm

5.Water-Soluble Ginkgo Biloba Extract 24/6

Water Solubility: 5g Ginkgo Biloba Extract will be dissolved completely in 100g water

Total Ginkgo Flavone Glycosides 24.0%

Total Terpene Lactones 6.0%

Ginkgolic acid <5.0ppm

[Appearance] Light yellow fine powder

[Particle size] 80 Mesh

[Loss on drying] £ 5.0%

[Heavy Metal] £10PPM

[Extract solvents] Ethanol

[Storage] Store in cool & dry area, keep away from the direct light and heat.

[Package] Packed in paper-drums and two plastic-bags inside.

[Function]

Expanding blood vessel, resisting insufficient blood and oxygen deficit, increasing blood flow, improving cerebral arteries and distal

blood flow. Promoting cerebral circulation metabolism, improving memory function, resisting depression, resisting lipidic overoxidation,

protecting liver damage.

In clinic, curing high blood pressure, hyperlipoidemia, coronary heart disease, angina pectoris, arterial sclerosis, cerebral embolism,

senile dementia, primary and periodic dropsy, acute drumming in the ears, epicophosis, a variety of body function in disorder, dizziness

and so on.

Pumpkin face Mask

Pumpkin face Mask at home

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https://www.iitutor.com
Condensation polymers are formed when monomers join together, and in the process also form a separate small molecule such as a water molecule. The ends of the monomer molecules must have functional groups that can join with other functional groups on neighbouring molecules.
Condensation polymerisation is the process in which two monomers combine with the elimination of a smaller molecule. One way that two different monomers can combine and in doing so lose a molecule of water and represents condensation polymerisation. This process continues and each remaining end joins with another monomer—each time lengthening the chain. One way to think of this is a “head-to-tail” joining.
Synthetic condensation polymers include nylons and polyesters. Natural condensation polymers include cellulose, cotton, wool, and silk.
Cellulose is a complex carbohydrate or polysaccharide. It is the most abundant biopolymer in nature. Carbohydrates consist of molecules containing C, H and O atoms. Carbohydrates contain many alcohol functional groups.
• Cellulose consists of long chains of β-glucose monomers.
• Glucose is an example of a simple carbohydrate or monosaccharide.
Structure of glucose :
Glucose (C6H12O6) is a ring molecule. The carbon atoms in the ring are numbered as shown. The –OH functional groups may be orientated above or below the plane of the ring. These different orientations at C, produce the alpha and beta forms of the glucose monomers.
• Glucose is an organic compound
• Ring can open up in solution to form a straight-chain structure. Open and chain forms are in equilibrium that cause glucose to exist as anomers, β-glucose and α-glucose.
Biopolymer is a naturally occurring polymer such as cellulose, starch, gluten, DNA and protein.
Formation of cellulose:
Cellulose is a condensation polymer which is formed when glucose monomers condense together through beta-1,4-glycosidic bonds. This involves a reaction between the –OH groups at the C1 and C4 carbons of adjacent glucose molecules.
The process begins by the condensation reaction between two glucose monomers to form a beta-maltose dimer. A water molecule is eliminated during this reaction. More glucose monomers condense and the chain grows until about 10 000 glucose monomers are linked in long, unbranched, ribbon-like strands.
Strong hydrogen bonding exists between –OH groups of neighbouring, close-packed strands. This produces a water-insoluble polymer with great strength and rigidity. Plants use cellulose as a structural carbohydrate for their cell walls.