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| Other Name: | Melanotan II | CAS No: | 121062-08-6 |
|---|---|---|---|
| MF: | C50H69N15O9 | EC Number: | 1308068-626-2 |
| Categories: | Pharmaceutical Intermediates | Purity: | 99.0%min |
| Appearance: | White Powder | Density: | 1.43 |
| Packing: | Vival | Shelf Life: | 2 Years |
| High Light: | Melanotan II121062-08-6,Melanotan II 10mg |
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Product Name :MT-II
Chemical Name:Melanotan II Acetate
Sequence:Ac-Nle-cyclo(Asp-His-DPhe-Arg-Trp-Lys)-NH2
CAS No.:121062-08-6
Molecular Formula: C50H69N15O9
Molecular Weight:1024.18g/mol
Specifition: 10mg/Vials
Purity : 98% HPLC
Biological Half-Life:33Hours
Appearance: White freeze-dried powder
Typical use:SkinTanning , enhance libido and Fat loss.
Standard Packing : 10Vials/Kits
Shelf Life :2 years
Storage:Refrigeration keep dry and away from light.
| Product Name: | Melanotan II |
| Synonyms: | Acetyl-(Nle4,Asp5,D-Phe7,Lys10)-cyclo-α-MSH (4-10) aMide Melanotan II, MTII, BreMelanotide aMide;MelanotanII Acetate(MT-2);AC-NLE-CYCLO(-BETA-ASP-HIS-D-PHE-ARG-TRP-EPSILON-LYS-NH2);AC-NLE-CYCLO[(BETA-D)-HFRW-(EPSILON-K)]-NH2;AC-NLE-CYCLO(-ASP-HIS-D-PHE-ARG-TRP-LYS-NH2) ACETATE SALT;AC-NLE4-C[ASP5, D-PHE7, LYS10]ALPHA-MSH (4-10)-NH2;AC-[NLE4, ASP5, D-PHE7, LYS10]-ALPHA-MSH (4-10)-NH2;(AC-NLE4, ASP5, DPHE7, LYS10)-CYCLO-ALPHA-MSH (4-10) AMIDE |
| CAS: | 121062-08-6 |
| MF: | C50H69N15O9 |
| MW: | 1024.18 |
| EINECS: | 1308068-626-2 |
| density | 1.43 |
| RTECS | OL4225000 |
| storage temp. | Keep in dark place,Sealed in dry,Store in freezer, under -20°C |
| solubility | H2O: 5 mg/mL, soluble |
| pka | 13.00±0.70(Predicted) |
| form | solid |
| color | white |
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Description:
What is Melanotan II?
Melanotan II (CAS NO.121062-08-6) was first synthesized at the University of Arizona. Researchers decided to find a more potent and stable alternative, one that would be more practical to defenses against skin cancer.
The researchers headed by Victor Hruby, found a peptide, [Nle4, D-Phe7]-α-MSH, that was approximately 1,000 times more potent than natural α-MSH after synthesizing and
screening hundreds of molecules. They dubbed this new peptide, "Melanotan" (later Melanotan I, now known as afamelanotide). They subsequently developed another analog, Ac-Nle-cyclo[Asp-His-D-Phe-Arg-Trp-Lys]-NH2), which they named "Melanotan Acetate".
Since their discovery, numerous studies dating back to the mid-1980s have found no obvious toxic effects of the Melanotan peptides. The scientists hoped to use Melanotan peptides to combat melanoma by stimulating the body's natural tanning mechanism to create a tan without first needing exposure to harmful levels of UV radiation. This in turn, they hypothesized, could reduce the potential for skin damage that can eventually lead to skin cancer.
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