chemical-categories

 

99% Purity Pharmaceutical Raw Materials Chlorhexidine Acetate For Antiinflammatory 56-95-1

 

Chlorhexidine Acetate Basic Info.:

 

Product Name: Chlorhexidine Acetate

CAS: 56-95-1

EINECS: 200-302-4

MF: C26H38Cl2N10O4

MW: 625.55

Assay: 99.5%

Appearance: White Crystalline Powder

Quality: Refined

Type: Pharmaceutical Intermediate

Melting Point: 154-155

Export Markets: Global

 

Chlorhexidine Acetate Descriptions:

 

1. It is a compound that contains chlorohexidine as an active ingredient. 

2. It possesses antiseptic properties and is widely used as a topical applicator and a bactericide because of the effect of chlorohexidine in killing both gram-positive and gram-negative bacteria.

3. It does so by inhibiting the growth of bacteria by interfering with the microbe's metabolism through interference with protein production of the bacteria as well as its DNA replication process. The chemical acts as a broad spectrum antiseptic.

 

Chlorhexidine Acetate Usage:

 

1.For topical broad-spectrum antimicrobial, bactericidal drugs against gram-negative and gram-positive bacteria have strong antibacterial, bactericidal capacity.

2.Disinfectants. Gram-positive and Gram-negative bacteria and fungi have a strong bactericidal effect on Pseudomonas aeruginosa is also effective. For skin disinfection, wash the wound, can also be used to disinfect surgical instruments.

3.Cation broad-spectrum antibiotic, belonging biguanide family. Its mechanism of action involves disrupting the bacterial cell membrane. Also disinfectants. Gram-positive and Gram-negative bacteria and fungi have a strong bactericidal effect on Pseudomonas aeruginosa is also effective. For skin disinfection, wash the wound, can also be used to disinfect surgical instruments.

 

 

99.9% Local Anesthetic Levobupivacaine HCl Powder Levobupivacaine Hydrochloride 5875-06-9 

 

Levobupivacaine HCL Basic Info.:

 

Product Name: Proparacaine hydrochloride 

Synonyms: Proparacaine HCl; Proparacaine Hydrochloride

CAS: 5875-06-9 

Molecular formula: C16H27ClN2O3 

Molecular Weight: 330.85 

EINECS number: 227-541-7 

Related Categories: API 

Use:anesthetic (local),Pharmaceutical raw materials

Packing:Foil bag or as requirments

 

Levobupivacaine HCL Description:

 

Levobupivacaine (rINN) is a local anaesthetic drug belonging to the amino amide group. It is the S-enantiomer of bupivacaine.

The hydrochloride salt of levobupivacaine, an amide derivative with anesthetic property. Levobupivacaine reversibly binds voltage-gated sodium channels to modulate ionic flux and prevent the initiation and transmission of nerve impulses (stabilizing neuronal membrane), thereby resulting in analgesia and anesthesia. In comparison with racemic bupivacaine, levobupivacaine is associated with less vasodilation and has a longer duration of action.

 

Levobupivacaine HCL Applications:

 

Levobupivacaine is the S-enantiomer of bupivacaine hydrochloride and is chemically described as (S)-1-butyl-2-piperidylformo-2', 6'-xylidide hydrochloride.

Levobupivacaine is a member of the amino amide class of local anaesthetics. It is indicated for surgical anesthesia and postoperative pain management.

 

 

High Purity Male Sex Hormones Vardenafil HCL / Levitra For Sex Enhancer Powder 224785-91-5

 

Vardenafil HCL Basic Info:

 

Product Name: 

Synonym: Fardenafil; Vardenafil hydrochloride

CAS No: 224785-91-5

MF: C23H33ClN6O4S

MW: 525.06

Purity: 99%

Melting point: 214-216°C

Half life: 4-5 hours

Appearance: White to Off-White Cyrstalline Solid, odorless, taste bitter and astringent soluble in water and alcohol.

Storage: in a cool and dry well-closed container and in ventilated area.

Product Categories: Intermediates & Fine Chemicals;Pharmaceuticals;Vardenafil

Usage: A selective phsphodiesterase type 5 (PDE5) inhibitor.

 

Vardenafil HCL Description:

 

Vardenafil (INN) is a PDE5 inhibitor used for treating erectile dysfunction. Vardenafil's indications and contra-indications are the same as with other PDE5 inhibitors; it is closely related in function to sildenafil citrate (Viagra) and tadalafil (Cialis). The difference between the vardenafil molecule and sildenafil citrate is a nitrogen atom's position and the change of sildenafil's piperazine ring methyl group to an ethyl group. Tadalafil is structurally different from both sildenafil and vardenafil. Vardenafil's relatively short effective time is comparable to but somewhat longer than sildenafil's.

 

Vardenafil HCL Application:

 

Beyond its indications for erectile dysfunction, vardenafil may be effective in the treatment of premature ejaculation, where it may significantly increase the time from vaginal penetration to ejaculation.Vardenafil, as with all PDE5 inhibitors, should not be used by men taking nitrate medications, because combining them with vardenafil might provoke potentially life-threatening hypotension (low blood pressure).

 

Further, Vardenafil causing lengthening of the QT interval. Therefore it should not be taken by men taking other medications that affect the QT interval (such as amiodarone).

 

 

High Purity White Crystalline Powder Hair Growth Powder 38304-91-5 Minoxidil For Hair Loss

 

Minoxidil Basic Info.:

 

Product Name: Minoxidil

Alias: Minoxidil / Loniten / Lonolox / Minona

CAS: 38304-91-5

Molecular Formula: C9H15N5O

Molecular Weight: 209.3

Purity: 99%

Standard: USP

Appearance: White Powder

Using: for anti-hair loss and high blood pressure

 

Minoxidil Desc:

 

Minoxidil is an antihypertensive vasodilator medication. It also slows or stops hair loss and promotes hair regrowth. Now off-patent, it is available over-the-counter for the treatment of androgenic alopecia.Widely used for the treatment of hair loss, it has been proven clinically effective in both the prevention of loss and in establishing varying degrees of hair re-growth in males and females suffering pattern baldness. Minoxidil must be used indefinitely for continued support of existing hair follicles and the maintenance of any experienced hair regrowth.

 

Product Application of Minoxidil:

 

Minoxidil was the first drug approved by the FDA for the treatment of androgenetic alopecia (hair loss). Before that, minoxidil had been used as vasodilator drug prescribed as oral tablet to treat high blood pressure, with side effects that included hair growth and reversal of male baldness. In the 1980s, UpJohn Corporation came out with a topical solution of 2% minoxidil, called Rogaine, for the specific treatment of androgenetic alopecia. Since the 1990s, numerous generic forms of minoxidil have become available to treat hair loss while the oral form is still used to treat high blood pressure.

 

The popularity hair loss treatment is due to the general preference in the overall population for the cosmetic appearance of a full head of hair. Minoxidil is used to stimulate hair growth in areas of the scalp that have stopped growing hair. As of early 2001, the exact mechanism of action of minoxidil is not known.

 

 

Natural Herbal Viagra Maca Extract Pharmaceutical Raw Materials For Men Sexual Enhancement

 

Maca Extract Basic Info:

 

Product Name: Maca Extract

Maca Root Extract; Maca Extract

Model: 4:1 10:1 20:1 TLC

English name: Peruvian Maca Root Extract Powder

Latin name: Lepidium meyenii

Active ingredients: Beta Ecdysone

Appearance: Brownish Yellow Powder

Origin: Root

Specification: Ratio Extract: 4:1 10:1 20:1

Test Method: TLC

 

Maca Extract Description:

 

Maca extract is taken from the root of the maca plant. It is consumed as a root vegetable and it grows naturally in Peru. This extract is thought to have many health benefits and healing properties. There are many ways to prepare maca extract, including drying the roots and grinding them into a fine powder or boiling the roots to extract the natural oils. The extract typically is sold in a liquid or a gel-like capsule.

 

Maca is a cruciferous plant Lepidium in the shape of radish-like hypertrophy of the roots, originating in Peru and Central's (Jinin) and Pasco (Pasco) near the Andes above 4,000 meters, the area cold, strong winds, eco- harsh conditions unsuitable for other crops, and thus Mame a source of food for Inca.. Maca can increase with physical, energetic, eliminate anxiety and improve sexual function. Its fresh roots can eat with meat and vegetables , also be dried food cooked with water or milk.

 

Body builders or people who are trying to lose weight can sometimes benefit by taking maca extract. It contains many vitamins and minerals as well as amino acids, which help to boost themetabolism and this makes the body run more efficiently. Amino acids can also help to improve muscle structure. Maca extract is sometimes used as an alternative to dangerous anabolic steroids used by body builders to improve muscle mass.

 

Maca Extract Application:

 

The nutritional value of dried maca root is high, similar to cereal grains such as rice and wheat. The average composition is 60-75% carbohydrates, 10-14% protein, 8.5% dietary fiber, and 2.2% fats. Maca is rich in the dietary minerals calcium and potassium (with low content of sodium), and contains the essential trace elementsiron, iodine, copper, manganese, and zinc as well as fatty acids including linolenic acid, palmitic acid, andoleic acids, and 19 amino acids.

 

Maca is consumed as food for humans and livestock, suggesting any risk from consumption is rather minimal. It is considered as safe to eat as any other vegetable food. However, maca does contain glucosinolates, which can causegoiters when high consumption is combined with a diet low in iodine. This being said, darker colored maca roots (red, purple, black) contain significant amounts of natural iodine, a 10-gram serving of dried maca generally containing 52 µg of iodine. Though this is common in other foods with high levels of glucosinolate, it is uncertain if maca consumption can cause or worsen a goiter.

 

Small-scale clinical trials performed in men have suggested that maca extracts can improve semen quality, and boost libido. A small double-blind, randomized, parallel group dose-finding pilot study has shown that Maca root may alleviate SSRI-induced sexual dysfunction.A 12-week randomized, double-blind, placebo-controlled study in 56 subjects found that Maca has no effect on sex hormone levels in men, including LH, FSH,prolactin, 17-OH progesterone, testosterone or estradiol.

 

A recent review states "Randomized clinical trials have shown that maca has favorable effects on energy and mood, may decrease anxiety and improve sexual desire. Maca has also been shown to improve sperm production, sperm motility, and semen volume." In total over 160 studies into the health effect of Maca have been indexed by the United States National Library of Medicine,National Institutes of Health.However, a 2010 review of the extant evidence for the effect of Maca on libido found only tentative support for its aphrodisiac claims.

 

Maca Extract Function:

 

Adaptogenic Properties

Maca root considered an adaptogenic herb. Adaptogenic herbs help increase the bodies resistance to stress whether the stress is a physical or emotional ailment it doesn’t matter. Adaptogens helps normalize body functions one in particular is to restore proper adrenal gland and endocrine functions.

 

Balance Hormones

One of the best benefits to using maca is its ability to balance hormones naturally. It makes Maca great for a variety of hormonal disorders such as PMS( Pre-menstrual syndrome), menopause, andropause and various other conditions which involve unbalanced hormones. Maca does not stimulate production or directly work any particular hormone, its hormone balancing effects come from its adaptogenic properties which aid the adrenal glands and support the endocrine system.

 

Increase Energy

Much like other adaptogenic herbs, maca provides a non central nervous stimulating and adrenal gland friendly way to naturally increase energy. Adaptogenic herbs support the adrenal glands and don’t cause burn out like various other CNS stimulants such as caffeine. Maca has also been shown to increase stamina and endurance.

 

Increase Libido/Sex Drive

Another of maca most prized benefits is its ability to increase libido and boost sex drove. Studies have shown maca can heighten libido and sexual desire and may alleviate SSRI induced erectile dysfunction. If that wasn’t enough maca has shown in studies to boost fertility by increasing sperm quality, volume, motility and production.

 

Rich Source of Nutrients

Maca is a source of nutrients such as amino acids, fatty acids, sterols, vitamins, minerals such as selenium, calcium, magnesium, and iron. Maca is also rich in over 60 health boosting phyto-chemicals/compounds which are where a lot of its benefits stem from also.

 

 

Pentadecapeptide Bpc 157 Human Growth Hormone Supplements Peptide Peptide Drum 137525-51-0

 

Pentadecapeptide Bpc 157 Basic Info.

 

Product Name: Pentadecapeptide Bpc 157

Alias: Booly Protection Compound 15, Pentadecapeptide, BPC 157;

Sequence: Gly-Glu-Pro-Pro-Pro-Gly- Lys-Pro-Ala-Asp-Asp-Ala-Gly-Leu-Val 

CAS: 137525-51-0 

MF: C62H98N16O22 

MW: 1419.53552 

Purity: 99% 

Specification: 2mg/vial 

Appearance: White Lyophilized Powder 

Standard: USP 

Certification: SGS 

Method of Analysis: HPLC 

Storage: Lyophilized peptides although stable at room temperature for 3 months, should be stored desiccated below -18°C. Upon reconstitution of the peptide it should be stored at 4°C between 2-21 days and for future use below -18°C. 

 

Pentadecapeptide Bpc 157 Description:

 

Pentadecapeptide BPC 157, composed of 15 amino acids, is a partial sequence of body protection

compound (BPC) Pentadecapeptide BPC 157, composed of 15 amino acids, is a partial sequence 

of body protection compound (BPC) that is discovered in and isolated from human gastric juice.

The promoting effect of pentadecapeptide BPC 157 on tendon healing involves tendon outgrowth, 

cell survival, and cell migration

 

Stable gastric pentadecapeptide BPC 157 (GEPPPGKPADDAGLV, M.W. 1419) may be the new drug stable in human gastric juice, effective both in the upper and lower GI tract, and free of side effects.

 

BPC 157, in addition to an antiulcer effect efficient in therapy of inflammatory bowel disease (IBD)(PL 14736) so far only tested in clinical phase II, has a very safe profile, and exhibited a particular wound healing effect. It also has shown to interact with the NO-saystem, providing endothelium protection and angiogenic effect, even in severely impaired conditions (i.e., it stimulated expression of early growth response 1 gene responsible for cytokine and factor generation and early extracellular matrix (collagen) formation (but also its repressor nerve factor 1- A binding protein-2)), important to counteract severe complications of advanced and poorly controlled IBD. Hopefully, the lessons from animal studies, particularly advanced intestinal anastomosis healing, reversed short bowel syndrome and fistula healing indicate BPC 157s high significance in further IBD therapy. Also, this supportive evidence (i.e., no toxic effect, limit test negative, LD1 not achieved, no side effect in trials) may counteract the problems commonly exercised in the use of peptidergic agents, particularly those used on a long-term basis

 

Pentadecapeptide Bpc 157 Application:

 

1. BPC 157 has a strong anti-inflammatory activity in both acute and chronic inflammation models. In fact, preliminary results in clinical trials suggest that BPC 157 may become an important therapeutic tool for the treatment of inflammatory bowel disease.

 

2. BPC 157 was shown to accelerate wound healing and to have a marked angiogenic effect. In addition, it significantly facilitates the healing of bone fracture in rats. This peptide also exhibits an osteogenic effect significantly improving the healing of segmental bone defect. BPC 157 accelerates the healing of transected rat Achilles tendon and transected rat quadriceps muscle.

 

3. FITC-phalloidin staining was able to demonstrate that BPC 157 induces F-actin formation in fibroblasts. Likewise, Western blot analysis was able to detect the production and activation of paxillin and FAK proteins. The western blot analysis also showed that BPC 157 increases the extent of phosphorylation of paxillin and FAK proteins without affecting the amounts produced.

 

 

S4 Most Effective Sarm Supplement Andarine Muscle Building Raw Steroids Powder 401900-40-1

 

Andarine Basic Info:

 

Product name: Andarine

Synonyms: Andarine;S4;S-4;GTX-007

CAS No.: 401900-40-1

MF: C19H18F3N3O6

MW: 441.36

Purity: 99.92%

Product categories APIs; Amines; Aromatics; Chiral Reagents; Intermediates & Fine Chemicals; Pharmaceuticals; SARMS

Appearance: White crystalline powder

Natural Bodybuilding SARM Powder Andarine S4 GTX-007 High Purity CAS 401900-40-1

 

Andarine Description:

 

Selective androgen receptor modulators or SARMs are a novel class of androgen receptor ligands. They are intended to have the same kind of effects as androgenic drugs like anabolic steroids but be much more selective in their action, allowing them to be used for many more clinical indications than the relatively limited legitimate uses that anabolic steroids are currently approved for.

 

S-4 is an experimental or investigation-stage proprietary SARM research chemical developed by GTx Inc for treatment of benign prostatic hypertrophy, muscle wasting, and osteoporosis. S-4 is considered a partial agonist of the androgen receptors in target tissue. S-4 has less pronounced anabolic and androgenic compared to other SARMs. In trials treating BPH induced in animal models, S-4 reduced prostate weight as effectively as finasteride and without producing any reduction in muscle mass or other side effects common with androgen receptor binding compounds. Gao et al suggest that by binding to androgen receptors, S-4 prevents DHT from binding and activating, but bypasses the expected anti-androgenic effects that would occur from occupying androgen receptors due to the fact that S-4 itself is a partial agonist of androgen receptors. S-4 has also been shown to prevent bone loss, reduce body fat, and improve muscle strength and body composition in orchidectomized and ovariectomized rats.

 

Andarine Application:

 

S4 Andarine is an orally active partial agonist for androgen receptors. It is less potent in both anabolic and androgenic effects than other SARMs. In an animal model of benign prostatic hypertrophy, andarine was shown to reduce prostate weight with similar efficacy to finasteride, but without producing any reduction in muscle mass or anti-androgenic side effects.

 

Andarine Function:

 

1. 1/3 as androgenic as testosterone in muscle tissue.

2. Anabolic at doses above 50mg.

3. Great for strength.

4. Great for muscle hardness.

5. Great for enhanced vascularity.

6. Great for endurance (aerobic or anaerobic).

7. Accelerated fat loss above 50mg.

8. Joint healing effects.

 

 

USP Grade Pharmaceutical Raw Materials 99%Min Idebenone For Cerebral Infarction 58186-27-9

 

Idebenone Basic Info.:

 

Product Name: Idebenone

CAS: 58186-27-9

Chemical name: 6-(10-Hydroxydecyl)-2,3-dimethoxy-5-methyl-1,4-benzoquinone

Molecular formula: C19H30O5

Molecular weight: 338.44

Melting point: (52- 55 °C )

Loss on drying: ≤ 0.5%

Relevant impurities(HPLC ): ≤ 0.8%

Content(HPLC ): ≥ 99.5%

Packing specification: 5Kg / tin, 25Kg / tin

Storage: Sealed and stored at room temperature.

Executive standard:Enterprise standard

Appearance: Orange yellow or orange crystalline powder, odorless, flavorless.

Property: This product is orange yellow or orange crystalline powder, soluble in methanol, ethanol, insoluble in water, odorless, flavorless.

Used for cerebral infarction, cerebral hemorrhage and cerebral artery sclerosis associated with depression, such as language barriers and intelligence impairment, etc.

 

Idebenone Introduction:

 

Idebenone is a kind of new drug for treating senile dementia and improving mental symptom. Also, it is a better antioxidant in cosmetics and health care than Coenzyme Q10 and Vitamin.

 

Idebenone is a modified version of coenzyme Q10 (CoQ10), which is absolutely crucial for metabolic function. Without it, the electron respiratory chain breaks and cells cannot produce energy. It is also the only lipid-soluble antioxidant that is synthesized in our bodies. Natural levels of CoQ10 begin to decrease after age 30.

 

CoQ10 would be a perfect supplement for athletes that expend excessive energy or push the anaerobic envelope were it not for one important detail: under hypoxic conditions (like going anaerobic), CoQ10 becomes pro-oxidative and creates a powerful free radical that can damage DNA, mitochondria, and lipid membranes.

 

There is a synthetic variation of CoQ10 called ubiquinol, also known as idebenone. It has been formulated to have all the advantages of CoQ10 without the pro-oxidative drawback.