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Trenbolone acetate
CAS No. 10161-34-9
Trenbolone acetate ( RU-1697;17beta-TBOH )
Catalog No. M10083 CAS No. 10161-34-9
Trenbolone acetate (RU-1697,17beta-TBOH) is a potent testosterone analog and selective androgen receptor modulator.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 10MG | 49 | In Stock |
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| 25MG | 76 | In Stock |
|
| 50MG | 110 | In Stock |
|
| 100MG | Get Quote | In Stock |
|
| 200MG | Get Quote | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
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Biological Information
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Product NameTrenbolone acetate
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NoteResearch use only, not for human use.
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Brief DescriptionTrenbolone acetate (RU-1697,17beta-TBOH) is a potent testosterone analog and selective androgen receptor modulator.
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DescriptionTrenbolone acetate (RU-1697,17beta-TBOH) is a potent testosterone analog and selective androgen receptor modulator, is an androgen ester and a long-acting prodrug of trenbolone; shows SARM-like effects as it binds to androgen receptors (ARs) with approximately three times the affinity of testosterone and has been shown to augment skeletal muscle mass and bone growth and reduce adiposity in a variety of mammalian species.
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SynonymsRU-1697;17beta-TBOH
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PathwayEndocrinology/Hormones
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TargetAndrogen Receptor (AR)
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RecptorAndrogenReceptor
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Research AreaEndocrinology
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Indication——
Chemical Information
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CAS Number10161-34-9
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Formula Weight312.40
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Molecular FormulaC20H24O3
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Purity>98% (HPLC)
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SolubilityDMSO: ≥ 44 mg/mL
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SMILESCC(O[C@H]1CC[C@@]2([H])[C@]3([H])CCC4=CC(CCC4=C3C=C[C@]12C)=O)=O
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Chemical NameEstra-4,9,11-trien-3-one, 17-(acetyloxy)-, (17β)-
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
1. Danhaive PA, et al. J Steroid Biochem. 1988 Jun;29(6):575-81.
2. Sinnett-Smith PA, et al. Horm Metab Res. 1987 Mar;19(3):110-4.
3. Ye F, et al. Steroids. 2014 Sep;87:59-66.
4. Yarrow JF, et al. Am J Physiol Endocrinol Metab. 2011 Apr;300(4):E650-60.
2. Sinnett-Smith PA, et al. Horm Metab Res. 1987 Mar;19(3):110-4.
3. Ye F, et al. Steroids. 2014 Sep;87:59-66.
4. Yarrow JF, et al. Am J Physiol Endocrinol Metab. 2011 Apr;300(4):E650-60.
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