CAS： 13103-34-9
MF： C30H44O3
Appearance： Light yellow oily matter
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Description |
Boldenone Undecylenate falls under the category of androgenic anabolic steroids, used primarily in veterinary medicine but also in bodybuilding and performance enhancement contexts. |
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Therapeutic Function |
Anabolic |
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Uses |
Boldenone Undecylenate is a synthetic anabolic-androgenic steroid (AAS) derived from testosterone. It is often referred to by its brand names like Equipoise or Parenabol. Initially designed for veterinary use, especially in horses, it was previously used in humans for muscle wasting conditions. It is administered via intramuscular injection and has a long-lasting effect due to its ester component, undecylenate, which delays its release into the bloodstream. |
| Chemical Structure | Boldenone is structurally similar to testosterone but has a double bond between carbon atoms 1 and 2, which reduces its androgenic and estrogenic activity. It is connected to the undecylenate ester, increasing its half-life in the body. |
| Mechanism of Action | Boldenone exerts its effects by binding to the androgen receptor in muscle tissues, which promotes protein synthesis and nitrogen retention. This increases muscle mass and reduces muscle breakdown. |
| Side Effects |
Androgenic: Estrogenic: Others: |
| Reference |
Boldenone undecylenate disrupts the immune system and induces autoimmune clinical hypothyroidism in rats: Vitamin C ameliorative effects [International Immunopharmacology Volume 99, October 2021, 107939] Effects of the anablolic steroid, boldenone undecylenate, on certain reproductive parameters in bulls [Theriogenology Volume 35, Issue 5, May 1991, Pages 893-906] |
InChI:InChI=1/C30H44O3/c1-4-5-6-7-8-9-10-11-12-28(32)33-27-16-15-25-24-14-13-22-21-23(31)17-19-29(22,2)26(24)18-20-30(25,27)3/h4,17,19,21,24-27H,1,5-16,18,20H2,2-3H3/t24-,25-,26-,27-,29-,30-/m0/s1
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boldenone undec-10-enoate
| Conditions | Yield |
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1-Dehydrotestosteron, Undecylensaeurechlorid;
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4-(bromomethyl)benzoic acid 1,1-dimethylethyl ester
boldenone undecenoate
bis(pinacol)diborane
C48H71BO7
| Conditions | Yield |
|---|---|
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With C9H12Br2N2NiO2; In 1,4-dioxane; at 30 ℃; for 12h; Inert atmosphere; Sealed tube;
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