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Global Hot Sell Anti Aging Coenzyme Q10 / Ubiquinol 303-98-0

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Global Hot Sell Anti Aging Coenzyme Q10 / Ubiquinol 303-98-0

Coenzyme Q10 Basic Info.:

Product Name: Coenzyme Q10

Synonyms: LABOTEST-BB LT00244787;COQ10;COENZYME Q10;Q-10;Q10 COENZYME;UBIDECARENONE;UBIQUINONE;UBIQUINONE-10 

CAS: 303-98-0 

MF: C59H90O4 

MW: 863.34 

EINECS: 206-147-9 

Chemical Properties Yellow-Orange Crystalline Powder 

Usage antioxidant, cardiovascular agent 

Usage Antibacterial and antioxidant for preventing and treating cancer. 

Usage Antibacterial, antioxidant 

Biological Activity Component of the mitochondrial transporter chain that behaves as a powerful antioxidant. Displays neuroprotective activity.

Ubidecarenone Details Of Coenzyme Q10:

Coenzyme Q10 (CoQ10 or ubiquinone) has a low risk of side effects and it is an essential vitamin-like substance with many health benefits. 

It is proven helpful in treating heart-related problems such as congestive heart failure and to lower high blood pressure. 

Coenzyme Q10 is a quinone, which is a substance that helps provide energy to cells in all oxygen-breathing organisms. Researchers first discovered coenzyme Q10 in 1957, and first named it ubiquinone, 

Because it was a quinone that was found in every cell of the body (the prefix ubi means everywhere). 

Later studies showed that ubiquinone acts as a coenzyme in the body, without which the three enzymes that provide energy to the body cannot function. 

Coenzyme Q10 Benefits: 

1. Anti-Aging As a strong antioxidant Q10 protects cells from chemicals and other harmful factors. 

2. Anti-oxidant Q10 naturally prevents our body and cells from free radicals damage and works as a shield against harmful effects. 

3. Muscles are also in need of this enzyme, due to its energy boosting quality. Experiments proved that people who had a balanced Q10 level were more energetic and vigorous 

4. Heart-related problems It is proven helpful in treating heart-related problems such as congestive heart failure and to lower high blood pressure. 

5. Improves immunity and can dramatically slow tumor growth. 

Coenzyme Q10 Application: 

1. Applied in pharmaceutical field, it can be used for treating cardiovascular disease. 

2. Applied in Cosmetics, it can be sued for skin whitening, removing wrinkling and slowing down ageing. 

 

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High Purity Dutasteride Avodart For Bodybuilding 164656-23-9

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Hot Sell Sexual Enhancement Ingredients--D (Xinyang base) USP

Xinyang base
Product Description:
Assay: 99%                              Packing:1kg/foil bag
HS Code:2937290023
Appearance: Light yellow crystalline powder, slightly soluble in water and slightly soluble in ethanol, soluble in lipids, odorless
 
Pharmaceutical theory: This ingredients belongs to phosphodiesterase type 5 of this kind of inhibitor. When sexuelle erregung, neurone of NANC and nitrogen oxide inendothelial cells synthase and catalyse L-arginine to synthetize nitrogen oxide, which activate guanosine to synthesis increase, then lead cavernous body of penis smooth muscle and artery of penis into relaxation, blood into penis sponge sinus, make penis erect. 
 
Usage: sexual function decline; non-organic sexual disorder, ED patients
 
OUR ADWANTAGE: 
1, High quality with competitive price: 
1)Standard: Enterprise Standard
2)We are manufacturer and can provide high quality products with factory price.
 
2, Fast and safe delivery
1)Parcel can be sent out in 24 hours after payment. Tracking number available
2)Secure and discreet shipment. Various transportation methods for your choice.
3)Customs pass rate ≥99%
4) We have our own agent/remailer/distributor who can help us ship our products very fast and safe, and we have stock in there for transferring.
 
3, We have clients throughout the world. 
1)Professional service and rich experience make customers feel at ease, adequate stock and fast delivery meet their desire.
2)Market feedback and goods feedback will be appreciated, meeting customers's requirement is our responsibility.
3) High quality, competitive price, fast delivery, first-class service gain the trust and praise from the customers
 
If you need this or you are interest in this kind of products, you are free to send me email or call me directly, we can talk more about the details of the products.
No matter you become a customer to me or not at last, you are welcome to inquire from me!
 
Tel: +86-731-22290218
Fax: +86-731-22290218
Cell: +8618188938027
E-mail: YCWlb031@yccreate.com
Skype:andyjake@outlook.com(Andy Xu)
 
 

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Nicotinamide Adenine Dinucleotide, Disodium Salt LAB GRADE 95%

NADH, Disodium Salt functions as a coenzyme of a large number of oxidoreductases.

NADH is the reduced form of nicotinamide adenine dinucleotide (NAD) that can donate electrons as part of a reducing reaction. In that process, NADH becomes oxidized to produce beta-NAD. A variety of enzymes use NADH plus Hydrogen ion to reduce substrates, generating beta-NAD as well as the reduced product. For example, NADH:ubiquinone oxidoreductase accepts two electrons from NADH and passes them to ubiquinone (coenzyme Q) as part of the mitochondrial electron transport chain.

NADH is a coenzyme that functions as a regenerating electron donor in catabolic processes including glycolysis, beta-oxidation and the citric acid cycle. As a reagent, NADH can be used in enzyme cycling assays to amplify detection of activity of biologically relevant enzymes or metabolites present in low concentrations.

β-Nicotinamide adenine dinucleotide (NAD) and β-Nicotinamide adenine dinucleotide, reduced (NADH) comprise a coenzyme redox pair (NAD:NADH) involved in a wide range of enzyme catalyzed oxidation reduction reactions. In addition to its redox function, NAD/NADH is a donor of ADP-ribose units in ADP-ribosylaton (ADP-ribosyltransferases; poly(ADP-ribose) polymerases ) reactions and a precursor of cyclic ADP-ribose (ADP-ribosyl cyclases).
As a reagent, NADH can be used in enzyme cycling assays to amplify detection of activity of biologically relevant enzymes or metabolites present in low concentrations.

Molecular Formula: C21H29N7O14P2 • 2Na
Formula Weight: 711.4

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Plant Extract Whitening Cosmetic Arbutin Arbutoside 497-76-7

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Plant Extract Whitening Cosmetic Arbutin Arbutoside 497-76-7
 
Arbutin Basic information
 
Product Name: Arbutin
Synonyms: 4-hydroxyphenyl-beta-d-glucopyranosid; Arbutin; Arbutoside
CAS: 497-76-7
MF: C12H16O7
MW: 272.25
EINECS: 207-850-3
Melting point: 195-198 °C
Alpha: -64 º (c=3)
Refractive index: -65.5 ° (C=4, H2O)
Storage temp.: 2-8°C
Solubility: H2O: 50 mg/mL hot, clear
Water Solubility: 10-15 g/100 mL at 20 ºC
Sensitive: Hygroscopic
Merck: 14,773
BRN : 89673
Stability: Stable. Hygroscopic - store under dry nitrogen.
Chemical Properties: Crystalline powder
Uses: Diuretic and anti-infective drugs of urinary system. Color photographic developing stabilizer. Whitening, anti-freckle, hair care in cosmetics.
Product Categories: Biochemistry;Glucose;Glycosides;Sugars;Natural Plant Extract;Herb extract;chemical reagent;pharmaceutical intermediate;phytochemical;standardized herbal extract;Uva, Ursi, p-Arbutin, Hydroquinone β-D-glucopyranoside;natural product;Inhibitors.
 
Product Description:
 
Alpha-Arbutin is a synthetic compound derived from natural plant sources. It is a water-soluble, white powder that remains stable in a pH range between 3.5 to 6.5. According to Lotion Crafters, a company offering skin care products, a 1 percent solution in clinical tests resulted in faster and better skin lightening after testing against other products for one month. Epidermal melanin biosynthesis, the effects of melanin on the skin, is blocked by Alpha-Arbutin; it reportedly works best when used for a period of two to three months.
 
Application:
 
1. Cosmetic industry:
Alpha Arbutin protect the skin against damage caused by free radicals Alpha Arbutin is a skin whitening agent which is very popular in Japan and Asian countries for skin de-pigmentation, Alpha Arbutin inhibits the formation of melanin pigment by inhibiting Tyrosinase activity. Alpha Arbutin is very safe skin agent for external use which does not have toxicity, stimulation, unpleasant odor or side effect such as Hydroqinone.The encapsulation of Alpha Arbutin constitute a delivery system to potentialize the effect in time.
 
2. Medical industry:
Back in the 18th century, Alpha Arbutin was first used in medical areas as an anti-inflammatory and antibacterial agent. Alpha Arbutin was used particularly for cystitis, urethritis and pyelitis. These uses still until today where natural medicine uses only natural ingredients to treat any disease. Also Alpha Arbutin may be used to repress the virulence of bacterial pathogens and to prevent contaminating bacteria, Alpha Arbutin is also used for treating allergic inflammation of the skin.
 
Function :
 
1.Alpha arbutin will relieve and dispell chloasma, melanin, acne ect;
2. Alpha arbutin has good effects of sterilization and relieving cough;
3. It used to alleviate pain of burn and scald,enhancing immune fuction;
4.It can promote skin elasticity, retaining skin moisture and slowing down aging skin;
5.It has function of restraining the activity of tyrosinase; preventing the formation of melanin.
 

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Purity 99% Female Hormone Chlormadinone Acetate CAS 302-22-7

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Purity 99% Female Hormone Chlormadinone Acetate CAS 302-22-7
 
Chlormadinone Acetate Basic Info.:
 
Product Name: Chlormadinone Acetate
CAS: 302-22-7
MF: C23H29ClO4
MW: 404.93
EINECS: 206-118-0
Mp: 212°C
Storage temp: -20°C Freezer
Appearance: Crystalline Solid
 
Chlormadinone Acetate Description:
 
Chlormadinone acetate (CMA) is a derivative of progesterone (17-acetoxy-6-chloro-4,6-pregnadiene-3,20-dione), first synthesized in 1961 and is used as an orally effective progestogen in hormone replacement therapy (HRT), and in combination with ethinyl estradiol (EE) in contraception since 1999. Chlormadinone acetate has a strong progestogenic effect about one-third higher than that of progesterone and may vary depending on the previous effect of an estrogen, i.e., estrogens may promote the formation of progesterone receptors and proliferation of the endometrium. Like progesterone, it is anti-estrogenic and has no partial androgenic effect (at the doses used for contraception and HRT). In contrast to progesterone, it has a slight glucocorticoid effect, a pronounced anti-androgenic effect and no anti-mineralocorticoid effect. No pregnancy-maintaining effect of CMA has been demonstrated in humans.
 
The anti-androgenic effect of CMA is presumed to be the result of both its binding to androgen receptors competitively inhibiting the effect of endogenous testosterone and dihydrotestosterone and the competitive inhibition of 5-reductase. In this respect, dosing of CMA is crucial; agonistic effects are observed when doses are increased from those optimal for an antagonistic effect.
 
Chlormadinone acetate has a strong anti-gonadotropic effect, through negative feedback on gonadotropin secretion, and has been used for more than 20 years alone for contraception in arterial risk patients. The clinical and metabolic tolerability of CMA has been demonstrated in numerous clinical studies with duration of treatment of up to 2.5 years.
The more recent application of CMA as an oral contraceptive in combination with EE (Neo Eunomin, Belara) has proven highly successful, with studies reporting excellent contraceptive efficacy, high tolerability and adherence due to a good side effect profile and positive effects on preexisting dysmenorrhea, skin and hair conditions.
 
Chlormadinone Acetate Application:
 
Chlormadinone acetate (CMA) is a derivative of naturally secreted progesterone that shows high affinity and activity at the progesterone receptor. It has an anti-estrogenic effect and, in contrast to natural progesterone, shows moderate anti-androgenic properties. CMA acts by blocking androgen receptors in target organs and by reducing the activity of skin 5alpha-reductase. It suppresses gonadotropin secretion and thereby reduces ovarian and adrenal androgen production. CMA shows high contraceptive efficacy by inhibiting ovulation due to its ability to suppress or disrupt endogenous gonadotropin secretion and, by this, inhibits follicular growth and maturation. In addition, it suppresses endometrial thickness and increases the viscosity of cervical mucus.
 

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Raw Medical Material Powder Priligy / Dapoxetine 119356-77-3

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Raw Medical Material Powder Priligy / Dapoxetine 119356-77-3
 
Dapoxetine Basic Info:
 
Product Name: Dapoxetine 
Synonyms: Priligy;Dapoxetine;Dapoxetine hydrochloride;Dapoxetine base;D-Dapoxetine HCL
CAS: 119356-77-3
MF: C21H23NO.ClH
MW: 341.88
EINECS: N/A
Purity: 99%
Appearance: White powder, odorless, slightly sweet, soluble in water and alcohol.
Product Categories: Erectile Dysfunction;API;Dapoxetine hydrochloride
  
Dapoxetine Description:
 
Premature ejaculation (PE) is the most common male sexual dysfunction. Dapoxetine hydrochloride, belonging to a class of drugs known as selective serotonin reuptake inhibitors or, was the first drug originally approved for the on-demand treatment of men with PE. We aimed to compare the intravaginal ejaculatory latency time (IELT), patient-reported global impression of change (PGIC), and adverse effect (AE) incidence associated with the use of dapoxetine (30 mg and 60 mg) versus placebo, and evaluate the differences in administering 60 mg versus 30 mg as on-demand medical oral therapy for the treatment of PE via a literature review and meta-analysis. Relevant randomized controlled trials (RCTs) were identified from PubMed, EMBASE, and Cochrane Central Register of Controlled Trials (Cochrane Library) databases. Ultimately, a total of seven RCTs with 8039 patients were included. Our meta-analysis demonstrated that dapoxetine (in the 30 mg and 60 mg subgroup) resulted in significantly higher IELT, PGIC, and AE incidence relative to the placebo, with higher proportions observed for 60 mg versus 30 mg of dapoxetine administration. The most common AEs were mild and tolerable. We conclude that dapoxetine (particularly the 60 mg dosage) may be considered a safe and effective drug for patients with PE.
 
Dapoxetine Application:
 
Dapoxetine hydrochloride is a drug that is used to treat premature ejaculation in men. It is available by prescription and is taken orally, prior to sexual intercourse. The drug belongs to the class called serotonin reuptake inhibitors (SSRIs), which have mainly been used to treat depression.
 
Sexual dysfunction, including premature ejaculation, is an extremely common condition worldwide. The cause of premature ejaculation has not been fully elucidated, but may include both psychological and physiological factors. Premature ejaculation refers to a short ejaculation time, which can affect the satisfaction of both partners during sexual intercourse.
 

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