Nanoactive Resveratrol (RES) 501-36-0

5% by HPLC

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Product Information

Product name	NanoActive Resveratrol (RES)
CAS No.	501-36-0
Quality Standard	5% by HPLC
Appearance	Yellow, viscous and transparent liquid
Solubility	Soluble in water and oil, heated to over 40℃, dissolution-rate will be accelerated

COA of NanoActive Resveratrol (RES)

ITEMS	STANDARDS	RESULTS
Characteristics	Light yellow, viscous liquid	conform
Diluted in water (1: 50)	Colorless or light yellow and transparent solution	conform
Odor	Characteristic Smell	conform
Assay (HPLC)	≥5.0%	5.10%
pH (in 1:50 aqueous solution)	5.0-8.0	6.8
Density (20ºC)	1.0 – 1.1 g/cm3	conform
Heavy Metal	≤10ppm	conform
Solubility	Soluble in water and oil, heated to over 40 ℃,	conform
Solubility	dissolution rate will be accelerated	conform
Total aerobic bacteria	< 10 CFU/g	conform
Molds and Yeasts	< 10 CFU/g	conform
pathogenic bacteria	negtive	conform
Conclusion: Conformed to specification.

Usage

Resveratrol (Res) is a non-flavonoid polyphenol compound. Resveratrol has a wide range of anti-cancer, anti-oxidation, antibacterial, anti-inflammatory activities. It can be widely used in medicine, health care products, food, cosmetics and other fields. Resveratrol highly works on many targets on the skin. As a new high- efficiency natural active substance, it can achieve good whitening, anti-wrinkle, anti-inflammation, antibacterial, acne treatment and anti-aging functions in skin care products. But disadvantages of resveratrol which is hard to dissolve in water, easily oxygenated and easy discoloration limit its application in cosmetics.

NanoActive Res, with a particle size of less than 30nm developed by the nano-delivery system (NSD), completely solve the problems of dissolution of Resveratrol. Resveratrol that stably wrapped in nano-carriers can greatly increase the absorption efficiency and bioavailability.

Resveratrol inhibits melanin synthesis by multiple targets

Product Efficacy of NanoActive Res

1. NanoActive Res can promote collagen synthesis, increase skin thickness and elasticity, remove wrinkles and tighten skin.
2. NanoActive Res inhibits melanin synthesis, reduces pigmentation and whitens skin
3. Remove free radicals to fight oxidation and anti-skin aging
4. NanoActive Res Promotes wound healing and reduces scarring
5. Cure acne and reduce acne pit
6. Antibacterial, anti-inflammatory, anti - sensitive and analgesia;

7. Prevent scarring and fibrosis

Low concentration of resveratrol (0.001%) reduced the melanin content of B16F10 cells by 50%

Resveratrol has an obvious anti-wrinkle effect

Recommended Quantity: 1-5%. The optimal pH range of the system is 3.0-6.5. The finished product should avoid direct sunlight (using opaque packaging). It is recommended to add UV absorbent to daycare products
Product storage: avoid light preservation under 25 ℃

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Fusidic acid 6990-06-3

Product Information Product name Fusidic acid; Fusidine CAS No. 6990-06-3 Molecular Formula C31H48O6 Molecular Weight 516.719 Quality Standard 97.5% up by HPLC Appearance White or almost white, crystalline powder COA ANALYSIS SPECIFICATION RESULTS Appearance White or almost white, crystalline powder White crystalline powder Solubility Practically insoluble in water, freely soluble in ethanol (96%) Practically insoluble in water, freely soluble in ethanol (96%) Identification IR: IR absorption spectrum of sample is in identical with that of reference substance IR absorption spectrum of sample is in identical with that of reference substance Reaction of sodium: The residue does not give reaction (a) of sodium The residue does not give reaction (a) of sodium Water 1.4%-2.0% 1.7% Sulfated ash ≤0.2% 0.1% Assay (on anhydrous basis) 97.5% - 101.0% 99.9% Particle size 90% Particle diamite < 20 μm 100% Particle diamite < 20 μm Related substance Impurity M ≤ 1.0% 0.1% Impurity G ≤ 0.7% Not detected Impurity L ≤ 0.5% Not detected Impurity B ≤ 0.4% Not detected Impurity A ≤ 0.3% Not detected Impurity H ≤ 0.10% Not detected Impurity C ≤ 0.2% Not detected Impurity D ≤ 0.2% Not detected Impurity F ≤ 0.2% Not detected Impurity I ≤ 0.2% Not detected Impurity K ≤ 0.2% Not detected Impurity K ≤ 0.2% Not detected Max unknown impurity ≤ 0.10% Not detected Total impurities ≤ 2.0% 0.1% Residual solvents Ethanol ≤ 5000pm Not detected Methanol ≤ 3000pm Not detected Ethyl acetate ≤ 5000pm Not detected N-hexane ≤ 290pm Not detected Microbial limit Bacteria ≤ 100cfu/g Not detected Total molds and yeasts ≤ 10cfu/g Not detected Staphylococcus aureus: None Not detected Pseudomonas aeruginosa: None Not detected Conclusion The sample complies with EP. Usage The application of Fusidic acid: Fusidic acid is primarily used as an antibiotic to treat bacterial infections. It is commonly applied topically, as a Fusidic acid cream or Fusidic acid ointment, to treat skin infections such as impetigo, infected cuts or wounds, and infected eczema. In some cases, it may also be prescribed orally or intravenously to treat systemic infections, particularly those caused by Staphylococcus aureus, including methicillin-resistant Staphylococcus aureus (MRSA). Additionally, fusidic acid has been used in combination with other medications for the treatment of various infections. For example, it may be combined with corticosteroids to treat inflammatory skin conditions or with hydrocortisone to treat otitis externa (outer ear infections). Fusidic acid works by inhibiting bacterial protein synthesis, specifically targeting the ribosomes within bacterial cells. This mechanism of action makes it effective against a wide range of bacteria, particularly Staphylococcus species. However, it is important to use fusidic acid judiciously to prevent the development of antibiotic resistance. *Products under the patent are only for R&D use