Active Member
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[China]
Address: Room 906, Block B, HaiyueTiandi, Shijiazhuang, Hebei, China
Contact name:Aimee
Hebei Chisure Biotechnology Co.,Ltd |
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Mail / Skype: aimee@speedgainpharma.com
Whatsapp: +8613292891350
SARMS Raw Powder MK677 CAS 159752-10-0 Ibutamoren MK-677 Powder:
| Product Name | Mk-677 |
| Mk-677 Alias | Ibutamoren |
| Mk-677 CAS | 159752-10-0 |
| Mk-677 Molecular Formula | C27H36N4O5S.CH4O3S |
| Mk-677 Molecular weight | 624.776 |
| Apperance | White Powder |
| Assay | 99% |
| Grade | Pharmaceutical Grade |
| Delivery time | 12h after your payment |
| Packing | Discreet package for delivery guarantee! |
| Delivery terms | HKEMS,DHL,TNT,EMS,Fedex,UPS |
| Payment | Western Union, Money gram, T/T,Bitcoin |
Ibutamoren mesylate (MK-677) is an orally active nonpeptide growth
hormone (GH) secretagogue. Nutrobal (Mk-677) was found to be very
safe. This is an amazing cutting stack with Cardarine and Andarine,
which will help melt off the stubborn fat and increase your muscle
mass.
Sarms MK-677 Powder Specification:
| TEST | ACCEPTANCE CRITERLA | RESULTS |
| TLC | Positive | |
| Identification | UV spectrum | Positive |
| IR spectrum | Positive | |
| Characteristics | White to yellowish-white crystalline powder | conform |
| Melting point | 32 ~ 37ºC | 33~36ºC |
| Specific optical rotation | +77°~+82° | +79.3° |
| Loss on drying | ≤0.5% | 0.15% |
| Assay | 97 ~ 103% | 99.08% |
| Free heptanoic acid | ≤0.2 % | 0.10% |
| Related substances | ≤2% | Pass |
| Acetone ≤100ppm | Pass | |
| Residual solvents(GC) | Methanol ≤100ppm | Pass |
| Pyridine ≤100ppm | Pass | |
| Particle size | Pass |
Sarms MK-677 Powder Application:
An experimental drug meant to control lipids and increase the level
of HDL, or good cholesterol, in the bloodstream. A cell-permeable,
thiazolyl compound that acts as a potent, high affinity, PPARd
agonist.
Usage An experimental drug meant to control lipids and increase the
level of HDL, or good cholesterol, in the bloodstream. A
cell-permeable, thiazolyl compound that acts as a potent, high
affinity, PPARδ agonist. Exhibits selectivity for PPARδ compared to
PPARα and PPARγ. Does not exibit any activity against other nuclear
or non-nuclear receptors. Reported to increase cholesterol efflux
and ABAC1 expression in macrophages, fibroblasts, and intestinal
cells.
Package:
3.Our Services:
We arel argest APIs, pharmaceutical intermediates and other
chemical products supplier in china, we have the best price in the
market.
Many local traders are buying our product and we also have foreign
buyers from Egypt,netherland,uk,poland and so on.
welcome big buyers contact us and meet for orders.
If you need sample,we can send it by a best price.And if you make a
larger order in the furture,we will return the sample fee to you.
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