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Octreotide Acetate

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Oral Anabolic Steroid Hormone Dianabol Methandienone Gain in Muscle Size 72-63-9

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Oral Anabolic Steroid Hormone Dianabol Methandienone Gain in Muscle Size 72-63-9
 
Methandienone Basic Info.:
 
Product Name: Metandienone
Alias: Dianabole, Dianabole,  Encephan, Geabol, Metanabol, Metandienon, Metandienonum, Metandrostenolon, Metandrostenolone, Metastenol, Methandrolone, Naposim, Nerobol, Nerobolettes, NSC-42722, Protobolin, Stenolon, Stenolone, Sterolon.
CAS: 72-63-9
MF: C20H28O2
MW: 300.43512
EINECS: 200-787-2
Purity: 99%
Melting point: 165-166 °C
Storage temp.: 2-8°C
Appearance: White powder.
Product Categories: Biochemistry;Hydroxyketosteroids;Steroids;Intermediates & Fine Chemicals;Pharmaceuticals;Steroid and Hormone;Finished Steroid and Hormone;API
Usage: 
(1)It can be should as medicines of androgens and anabolic hormones. 
(2)It can be used for treating expendable chronic disease, children mal-development, osteoporosis and hyperlipidemia.
(3)Anabolic steroid. Androgen. Controlled substance. 
 
Methandienone Description:
 
One of the most important anabolic steroids in bodybuilding ever since its introduction in 1958. Also commonly known as "Dbol", this oral compound is best used for steroid cycles in combination with injectable steroids, but can be of value used alone as well. Methandrostenolone is a derivative , and exhibits a strong anabolic effect along with a moderate androgenic effect. Methandrostenolone is also commonly known as 'dianabol' which is the old Ciba brand name. Methandrostenolone is an oral steroid, which is potent. 
 
Methandienone Applications:
 
One of the most important anabolic steroids in bodybuilding ever since its introduction in 1958. Also commonly known as "Dbol", this oral compound is best used for steroid cycles in combination with injectable steroids, but can be of value used alone as well.
 
(Dianabol) is the most well known Steroid in existance today and was considered by Arnold schwarzenegger to be the 'breakfast of champions'. Dianabol is a very strong compound and takes very litle time to take effect, by two weeks you will be noticing huge effects from this drug.
 
One of the great benefits of Dianabol is its ability to make one feel good inside, confident and powerful. All three are vastly important in performing well in the gym and Dianabol will certainly make you perform well in the gym! In the gym you will notice huge gains in strength and you will find that your muscle fill very full and large, this is mostly due to the fact that it dramatically increases protein synthesis and nitrogen retention within the muscle cells. - training on Dianabol is a great experience.
 
With regards to weight gains Dianabol is a champion at making the scales go up and almost nothing can do that faster than this compound. Because of this it is an ideal Steroid to take at the start of a Steroid cycle, what is known as a 'kick-start' and for this reason it is best used, and almost always used, in conjunction with injectable Steroids.
 
A typical dose would be 40-60mg/day and many serious Bodybuilders will go up to 100mg/day, however, it is important to note that Dianabol can impact your blood pressure levels at higher doses.
 

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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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Oral Anabolic Steroids Powder 7-Keto DHEA Acetate CAS 1449-61-2

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Oral Anabolic Steroids Powder 7-Keto DHEA Acetate CAS 1449-61-2
 
7-Keto-DHEA Acetate Basic Info.:
 
Product Name: Androst-5-en-3-ol-7,17-dione acetate
Synonyms: 10,13-dimethyl-7,17-dioxo-2,3,4,8,9,11,12,14,15,16-decahydro-1h-cyclopenta[a]phenanthren-3-yl acetate;7-KETO-DHEA;7-OXO-DEHYDROEPIANDROSTERONE ACETATE;7,17-dioxoandrost-5-en-3-yl acetate;androst-5-en-3-ol-7,17-dione acetate;3-BETA-ACETOXYANDROST-5-ENE-7,17-DIONE;3BETA-ACETOXY-17A-OXO-ANDROST-5-ENE-7,17-DIONE;3-ACETYL-7-KETO-DHEA
CAS: 1449-61-2
MF: C21H28O4
MW: 344.44
EINECS: N/A
Product Categories: Pharmaceutical Raw Materials;steroids
 
Description And Applications Of 7-Keto-DHEA Acetate:
 
7-keto-DHEA is a by-product of dehydroepiandrosterone (DHEA), a chemical that is formed in the body. 
DHEA is a "parent hormone" produced by glands near thekidneys. But unlike DHEA, 7-keto-DHEA is not converted to steroid hormones such as androgen and estrogen. Taking 7-keto-DHEA by mouth or applying it to the skindoes not increase the level of steroid hormones in the blood.
 
7-keto-DHEA might promote weight loss by speeding up the body's metabolism.
7-Keto is marketed as a dietary supplement with the implication that it may accelerate weight loss, increase metabolism, enhance memory, or prevent age-related changes. When used in a topical (skin lotion) product 7-Keto caused long-lasting changes in the body's levels of testosterone, epitestosterone, estradiol, and other steroid hormones. Researchers have raised concern that supplements may trigger positive tests for performance-enhancing drugs.
 

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Oral Finasteride / Proscar Steroids Powder For Hairloss Treatment 98319-26-7

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Oral Finasteride / Proscar Steroids Powder For Hairloss Treatment 98319-26-7
 
Finasteride Basic Info.
 
Product Name: Finasteride
Synonyms: Finasteride;Proscar;Prostide;
CAS: 98319-26-7
Molecular Formula: C23H36N2O2
Molecular Weight: 372.5441
Assay: 99%
Appearance: White or off-white crystal powder
Density: 1.066g/cm3
Boiling Point: 576.61°C at 760 mmHg
Flash Point: 177.448°C
Vapour Pressure: 0mmHg at 25°C
Usage: It is 5 alpha - reductase inhibitor that can inhibit testosterone to convert into DHT. Also used for the treatment of Hyperplasia of prostate. Finasteride is a 4-- aza-steroid compound which is a specific inhibitor of the metabolism of testosterone within dihydro testosterone become stronger during the cell type-II enzyme 5a-reductase. The enlarged prostate called benign prostatic hyperplasia or prostate depends on the conversion of testosterone to dihydro-testosterone.
 
Finasteride Description:
 
Finasteride is a popular anti-androgen medication manufactured by Merck most commonly known as either Proscar or Propecia. Based on the progesterone skeleton, Finasteride belongs to a class of medications known as 5alpha-reductase inhibitors and as such is used for the treatment revolving around type 2 5-AR based occurrences.
 
This is important for performance enhancers as DHT based anabolic steroids have specific side-effects that may occur that can largely be remedied with the use of a 5-AR inhibitor such as Finasteride. As a type 2 5-AR inhibitor Finasteride was designed for the purpose of treating hair-loss, prostate enlargement, as well as prostate cancer.
 
Finasteride is very common among those who supplement with anabolic steroids yet fear hair-loss but there are important things you need to understand before you consider Finasteride use. As an androgen suppressor Finasteride can seriously inhibit the gains made while on cycle, severely and on that basis it is not highly recommended for on-cycle hair preservation.
 
Finasteride Applications:
 
Propecia (finasteride) is used to treat male pattern baldness (androgenic alopecia) in men. Oral use though will reduce DHT levels systemically, which may adversely affect training and sex drive.
 
It is also used in combination with doxazosin in the treatment of benign prostatic hyperplasia (BPH).] Finasteride is an orally active testosterone Type II 5-alpha reductase inhibitor, inhibiting the enzyme that converts testosterone to dihydrotestosterone (DHT).
Topically (on the scalp itself) it is of some effect in minimizing further hair loss. In combination with Nizoral and spironolactone (which smells awful, by the way) it can actually reverse loss moderately.
 
For use in cycles with testosterone, I don't think it is bad at all. One simply doesn't want less DHT than normal. As the amount of testosterone in the system increases, the amount of finasteride needed to keep levels down to normal increases. I consider 5 mg/day reasonable at the gram per week level, and proportionally less at lower dosages of testosterone.
 

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Oral or Injection Trenbolones Steroids 6-Bronmandrostenedione For Gain Muscle 38632-00-7

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Oral or Injection Trenbolones Steroids 6-Bronmandrostenedione For Gain Muscle 38632-00-7
 
6-Bronmandrostenedione Basic Info.:
 
Product Name: 6-Bronmandrostenedione
Synonyms: (6b)-6-Bromoandrost-4-ene-3,17-dione; (6beta)-6-bromoandrost-4-ene-3,17-dione; 6-Bromoandrost-4-ene-3,17-dione
CAS RN.: 38632-00-7
Molecular Weight: 365.3046
Molecular Formula: C19H25BrO2
Density: 1.35g/cm3
Boiling Point(ºC): 467°C at 760 mmHg
Flash Point(ºC): 100.3°C
refractive_index: 1.577
Chemical Properties: Pale Yellow Solid
Usage: 6-Bronmandrostenedione analog, an aromatase inhibitor.
 
6-Bronmandrostenedione Description:
 
6-Bromodione is a fast acting competitive inhibitor of the aromatase enzyme. It works by binding to the aromatase enzyme to prevent it from aromatizing androgens. This is not a permanent binding and later acts to normalize aromatase (and thus estrogen levels) as hormone production returns to normal. It specifically targets aromatase and does not act as a central anti-androgen like some other post cycle products can. This means that your libido and mood will not be negatively affected.
 
6-Bronmandrostenedione Application:
 
6-beta-Bromodione works in a similar way but has an irreversible and permanent effect. This works well to mediate the excess aromatase that was produced while on cycle, while the alpha isomer works to normalize the natural levels. The goal is again to transition into normal production levels for all hormones affected by the anabolic cycle.
 

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Palmitoyl Tetrapeptide-7

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

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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.
 

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Peptides 170851-70-4 Weight Loss Steroids Ipamorelin For Muscle Gain

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Peptides 170851-70-4 Weight Loss Steroids Ipamorelin For Muscle Gain
 
Ipamorelin Basic Info.:
 
Product Name: Ipamorelin
Synonyms: IpoMarelin;IpaMorelin Acetate;Aib-His-D-2-Nal-D-Phe-Lys-NH2
Unit Size: 2 mg/vial
Unit Quantity: 1 Vial
CAS NO.: 170851-70-4
Molecular Formula: C38H49N9O5
Molecular Weight: 711.85
Sequence: H-Aib-His-D-2-Nal-D-Phe-Lys-NH2
Appearance: White Powder
Purity: 98.49%
Identity (ESI-MS) 711.85±0.5
Source Chemical Synthesis
Storage: Stable at room temperature for 90 days,however it should be stored in a freezer below -8°C for any extended period of time. After reconstituting Ipamorelin should be refrigerated at temperatures not to exceed 36°F.
 
Ipamorelin Description:
 
Ipamorelin is a fascinating new muscle building discovery that is getting a lot of attention in the bodybuilding world. It is a synthetic peptide that has powerful Growth Hormon releasing properties. And these GH releasing properties are what is of interest to athletes and bodybuilders since they can make a tremendous difference in the amount of muscle you can grow and how quickly you burn fat.
 
Ipamorelin is a penta-peptide. (Aib-His-D-2-Nal-D- Phe-Lys-NH2) And, the strength it displays may very well make regular old Growth Hormon (GH) obsolete. But what athletes and bodybuilders really want to know is what is this wonder peptide capable of doing, how is it used, and how does it compare to the other GHRP peptides?
 
Athletes are taking Ipamorelin in a 200mcg -300mcg dosage, two or three times daily, using a tiny insulin needle to inject. They usually start with the lower dose since side effects can include headaches or what feels like a head-rush. Ipamorelin can be taken at anytime but taking it about 30-45 minutes before a workout would seem ideal because of the pulse in Growth Hormon (GH) it creates allowing for maximum growth.
 
Studies on the effects of Ipamorelin on bone growth, body weight, and GH release showed some interesting conclusions.In one experiment, various doses were administered over the course of 15 days to test the group's reactions.
 
There was a distinct and dose-dependent effect on body weight gain however, the treatment group did not show a change in total IGF-I levels. Nor did the treatment group produce serum markers of bone development. For example, the number of cells in the wide portion of the tibia (the shinbone) did not change significantly. This is a good thing because it suggests muscle growth with less potential for deformity of bone or cartilage.
 
Ipamorelin in theory may increase Acetylchloine or Cortisol when used in higher dosages. However, and increase in Acetylchloine or Cortisol is even more likely with GHRP-2 and GHRP-6. In fact, in the case of Ipamorelin, there was little to no rise in Acetylcholine and Cortisol blood plasma levels even at injections more than 200 times higher than the effective dosage for comparable GH release.
 
Ipamorelin Applications:
 
Ipamorelin is a selective growth hormon secretagogue and agonist of the ghrelin receptor. In pentobarbital anaesthetised rats, ipamorelin released GH with a potency and efficacy comparable to GHRP-6 (ED50 = 80±42 nmol/kg and Emax = 1545±250 ng GH/ml vs 115±36nmol/kg and 1167±120ng GH/ml). In conscious swine, ipamorelin released GH with an ED50 = 2.3±0.03 nmol/kg and an Emax = 65±0.2 ng GH/ml plasma. Again, this was very similar to GHRP-6 (ED50 = 3.9±1.4 nmol/kg and Emax = 74±7ng GH/ml plasma). GHRP-2 displayed higher potency but lower efficacy (ED50 = 0.6 nmol/kg and Emax = 56±6 ng GH/ml plasma). The specificity for GH release was studied in swine.
 

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