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Safe Human Growth Hormone Peptide PT 141 Bremelanotide For Peptide Drum PT141 32780-32-8

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Safe Human Growth Hormone Peptide PT 141 Bremelanotide For Peptide Drum PT141 32780-32-8
 
PT 141 Basic Info.
 
Product Name: PT-141; PT141
CAS: 32780-32-8
MF: C50H69N15O10
MW: 1040.17736
Appearance: White powder
Water Content(Karl Fischer): ≤ 5.0%
Acetate Content(by HPLC): ≤ 15.0%
Amino Acid Composition: ± 10% of theoretical
Purity(by HPLC): ≥ 97.0%
Single Impurity(by HPLC): ≤ 1.0%
Peptide Content(by %N): ≥ 80%
Assay(By Anhydrous, Acetic Acid-free): 95.0~105.0%
Bacterial Endotoxins: ≤ 5EU/mg
Grade: Pharmceutical Grade
Storage: Shading, confined preservation
 
PT 141 Description:
 
PT-141 is a synthetic amino acid protein discovered during clinical trials using the Melanotan 2 for sunless tanning, photo-protection results from melanotans. Participants were documented as having experienced aphrodisiac reactions, leading to the further development PT-141. The melanocortin system targets receptors associated with desire through the melanocyte stimulating hormone paths that cross the blood-brain-barrier. Potentially the powerful sex-drug results feeling an aphrodisiac experience amplifying arousal pt141 reviews have shown the ability to increase libido effects of both men and women.
 
PT 141 Application:
 
PT-141 functions by activating the melanocortin receptor and MC4R namely. Bremelanotide originally was tested for nasal spray delivery but was discontinued after concerns about side effects. Bremelanotide PT141, as Melanotan II, may cause spontaneous arousal enhancing effect. Unlike other supplements, PT-141 results do not act on the vascular body, but directly increases desires through the nervous system.
 

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Tesamorelin Anabolic Androgenic Steroids Tesamorelin Intramuscular Injection 218949-48-5

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Tesamorelin Anabolic Androgenic Steroids Tesamorelin Intramuscular Injection 218949-48-5
 
Tesamorelin Basic Info.:
 
Product Name: Tesamorelin
Unit Size: 2 mg/vial 
Unit Quantity: 1 Vial 
C6H9O-Tyr-Ala-Asp-Ala-Ile-Phe-Thr-Asn-Ser-Tyr-Arg-Lys-Val-Leu-Gly-Gln-Leu-Ser-Ala-Arg-Lys-Leu-Leu-Gln-Asp-Ile-Met-Ser-Arg-Gln-Gln-Gly-Glu-Ser-Asn-Gln-Glu-Arg-Gly-Ala-Arg-Ala-Arg-Leu-NH2
CAS: 218949-48-5
Molecular Formula: C211H366N72O67S1
Molecular Weight: 5135.89
Appearance: white powder
Purity (HPLC): ≥99.00%
Packing: According to every customer's requirement.
 
Tesamorelin Description:
 
Tesamorelin is a synthetic peptide consisting of all 44 amino acids of hGRF with the addition of a trans-3-Hexenoic acid group.Tesamorelin (also known as Egrifta) is a synthetic form of growth-hormone-releasing hormone which is used in the treatment of HIV-associated lipodystrophy.tendon fibroblasts in a dose-dependent manner as revealed by transwell filter migration assay. BPC 157 also dose dependently accelerated the spreading of tendon fibroblasts on culture dishes. The F-actin formation as detected by FITC-phalloidin staining was induced in BPC 157-treated fibroblasts. The protein expression and activation of FAK and paxillin were determined by Western blot analysis, and the phosphorylation levels of both FAK and paxillin were dose dependently increased by BPC 157 while the total amounts of protein was unaltered. In conclusion, BPC 157 promotes the ex vivo outgrowth of tendon fibroblasts from tendon explants, cell survival under stress, and the in vitro migration of tendon fibroblasts, which is likely mediated by the activation of the FAK-paxillin pathway.
 
Tesamorelin Applications:
 
1. Triptorelin raises testosterone levels by causing constant stimulation of the pituitary, it decreases pituitary secretion of gonadotropins luteinizing hormone (LH) and follicle stimulating hormone (FSH). 
 
2. Like other GnRH agonists, triptorelin may be used in the treatment of hormone-responsive cancers such as prostate cancer or breast cancer, precocious puberty,estrogen-dependent conditions (such as endometriosis or uterine fibroids), and in assisted reproduction.
 

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((2R,3R,4R)-3-(benzoyloxy)-4-fluoro-4-methyl-5-oxotetrahydrofuran-2-yl)methyl benzoate 99%

More product information ,pls contact us as follow:
Shanghai Ansion pharma Technology Co.,Ltd
www.ansionpharma.com
ann.xu@ansionpharma.com

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(2R,4S)-5-([1,1'-biphenyl]-4-yl)-4-((tert-butoxycarbonyl)aMino)-2-Methylpentanoic acid 99%

Shanghai Ansion Pharma Technology Co.,Ltd
www.ansionpharma.com
ann.xu@ansionpharma.com

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1-Pentanone, 2-aMino-4-Methyl-1-[(2R)-2-Methyloxiranyl]-, (2S)-, trifluoroacetate (9CI) 99%

Shanghai Ansion Pharma Technology Co.,Ltd

www.ansionpharma.com

ann.xu@ansionpharma.com

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Factory Supply Muscle Building Steroids ATD / 1,4,6-Andorstatriene-3,17-Dione 144413-58-1

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Factory Supply Muscle Building Steroids ATD / 1,4,6-Andorstatriene-3,17-Dione 144413-58-1
 
ATD Basic information
 
Product Name: ATD
Synonyms: ADT;Androstatrienedione;ATD;Anthra[2,3-b:6,7-b']dithiophene;ADT AldrichCPR, sublimed;1,4,6-Androstatrien-3,17-Dione
CAS: 144413-58-1
MF: C19H22O2
MW: 282.38
EINECS: N/A
Product Categories: Materials Science;New Products for Materials Research and Engineering;Organic and Printed Electronics;Organic Field Effect Transistor (OFET) Materials;p-Type Organic Semiconductors;p-Type Small Molecules
Usage: A potential metabolitie of STS 557 (Dienogest). A steroid with antiglucocorticoid activity
 
Product ATD Description:
 
1,4,6-Androstatrien-3,17-dione (ATD) is considered to be a potent irreversible aromatase inhibitor that is useful for inhibiting estrogen biosynthesis by binding and inactivating aromatase in peripheral and adipose tissues in a permanent manner.
 
It is used to control estrogen synthesis and present in some of the over-the-counter muscle-enhancing and bodybuilding supplements. It increases testosterone levels in the body in an indirect manner and is therefore considered to be one of the favorite supplement among professional athletes and bodybuilders.
 
Application Of ATD:
 
1,4,6-Androstatrien-3,17-dione (ATD) offers benefits such as improvements in male fertility, mood levels, shortened recovery in case of burns or severe trauma and stimulation in developing mammals. It is considered to be a more effective anti-aromatase substance than many others and is potent enough to increase testosterone levels in the body without a concomitant reduction of the estrogen levels in men. It may be used for hormone or androgen replacement therapy in men without resulting in a concomitant reduction in endogenous estrogen levels when administered in an oral or transdermal way in dosages ranging from 25-150 mg/day.
 

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Oral Anabolic Steroids Anadrol Oxymetholone For Anemia Treatment And Anti-cancer 434-07-1

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Oral Anabolic Steroids Anadrol Oxymetholone For Anemia Treatment And Anti-cancer 434-07-1
 
Oxymetholone Basic Info.:
 
Product Name: Oxymetholone 
Alias: Anadrol
CAS No: 434-07-1
MF: C21H32O3
MW: 332.482
Purity: 99%
Melting point: 172-180°C
Alpha: 34 º
Refractive index: 38 ° (C=1, CHCl3)
Storage temp.: 2-8°C
Water Solubility: <0.1 g/100 mL at 23 ºC
Stability: Stability May be light sensitive. Combustible. Incompatible with strong oxidizing agents.
Quality standard: USP28/BP2005          
Apperance: Off-White to Pale Yellow Solid
Packing: as your require pack powder
Usage: Anabolic steroid. Controlled substance
 
Anadrol is the strongset effective oral steroid and oxymetholone(anadrol) has an extremely androgenic which hand in hand with an extremely intense anabolic component, by taking the oxymetho-lone(anadrol) the athletes experiences an enormous"pump effect"during the workout in the exercised muscles.
 
Oxymetholone Description:
 
Anadrol (Anadrol, Anadrol 50, Androyd) is one of the most popular anabolic steroids of all time in both performance and medical circles. It also represents one of the oldest steroids on the market. Provided by both Syntex and Park Davis & Co. in the 1960's, Anadrol hit the market in an effort to treat muscle wasting diseases, osteoporosis and any such related conditions. While still used for such purposes today, Anadrol is also used to treat the low red blood cell condition anemia, and in the U.S. is one of the only reasons the steroid is prescribed; most commonly to HIV patients.
 
While carrying numerous therapeutic benefits, many of which have been ignored by the FDA despite medical evidence, most who are interested in Anadrol are so for the purpose of performance enhancement. If it's good for treating a muscle wasting disease it's going to be good for building muscle mass, and this is the primary reason this steroid is a favorite of many performance enhancing athletes.
 
Anadrol is an extremely estrogenic steroid. A dihydrotestosterone (DHT) derivative, like all DHT compounds it does not aromatize but Anadrol still carries strong estrogenic traits. Due to this estrogenic nature as well as its tremendous anabolic nature, users of this steroid often report gains of 20-30lbs in only a few weeks, and that's not an exaggeration. This makes Anadrol one of the premier off-season steroids for many athletes, and overall that will be its only performance purpose in a general sense. Of course, as we'll see later on, competitive bodybuilders often use this steroid for contest prep at the very end, but in the grand scheme of things this is a bulking steroid.Due to its strong estrogenic nature coupled with its DHT composition, the side effects of Anadrol can be quite extensive. This steroid will carry nearly every last primary possible side effect of anabolic steroid use. Not only does this include things like gynecomastia, water retention, hair loss and acne, but it also includes liver toxicity. Anadrol is an oral steroid belonging to the C17-alpha alkylated (C17-aa) class of medications, and of all C17-aa steroids it is one of the most liver toxic.
 
While carrying only a moderate androgenic rating, Anadrol tends to display androgenic traits that are far beyond what its rating would imply. For this reason, Anadrol is not recommended to women as it will produce strong virilization symptoms. Women who are looking for anabolic assistance will find other DHT compounds such as (Anavar) or Methenalone (Primobolan) to be far more valuable as well as safer.
 
Like many anabolic steroids, Anadrol is plagued by myths and half-truths; however, in this case it may be a little more so. As we dive into this powerful anabolic steroid, we'll do our best to separate fact from fiction; we'll do our best to separate misconceptions about this steroid in comparison to Methandrostenolone (Dianabol), which are the most common misconceptions of all. We'll look at the primary Anadrol traits, how they translate into benefits, the side effects of the steroid, and of course, what you can do to avoid them and remain safe. We'll cover every last aspect of the Anadrol hormone, and enable your supplementation experience to be successful should you choose to undertake it.  
 
Oxymetholone Applications: 
 
Anadrol can be use in treating HIV wasting syndrome. Presented most commonly as a 50 mg tablet, oxymetholone is one of the strongest androgenic steroids available. Similarly, there is a risk of side effects. Despite very low binding affinity with the androgen receptor, oxymetholone is highly effective in promoting extensive gains in body mass, citation needed mostly by greatly improving protein synthesis.
 
For this reason, it is often used by bodybuilders and athletes. Many athletes also use anadrol as a method of protection for the joints under heavy loads. That's why anadrol is widely considered by bodybuilders to have the strongest anabolic effect out of all oral steroids available.    
 

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6-(2-chloro-5-fluoropyrimidin-4-yl)-4-fluoro-1-isopropyl-2-methyl-1H-benzo[d]imidazole 99%

Ansion pharma is a factory providing pharmaceutical intermediate and custom synthesis service. 
 
More products infomation, pls contact us: ann.xu@ansionpharma.com; www.ansionpharma.com

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

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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.
 

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

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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).
 

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