trestolone acetate

Basic information

  • Product Name:trestolone acetate
  • CasNo.:6157-87-5
  • MF:C21H30O3
  • MW:330.467

Physical and Chemical Properties

  • Purity:99%
  • Boiling Point:111-114 °C
  • Packing:
  • Throughput:
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Product Details

CasNo: 6157-87-5

MF: C21H30O3

Reliable Quality Chinese Factory Supply trestolone acetate 6157-87-5 In Stock

  • Molecular Formula:C21H30O3
  • Molecular Weight:330.467
  • Vapor Pressure:3.33E-08mmHg at 25°C 
  • Melting Point:111-114 °C 
  • Refractive Index:1.538 
  • Boiling Point:447.571 °C at 760 mmHg 
  • Flash Point:194.228 °C 
  • PSA:43.37000 
  • Density:1.117 g/cm3 
  • LogP:4.30590 

Trestolone acetate(Cas 6157-87-5) Usage

Side effects

Trestolone Acetate is quite obvious to offer negative side effects when is considered to be about 10 times more potent than testosterone. Side effects are only possible and they can be well reduced or completely avoided if you know how to use the compound properly.For example, if you would use a PCT plan at the end of the cycle all along with various meds (like Aromatase Inhibitors) and different cycle supporting supplements, without exceeding cycle length and dosage then you would be fine in most cases (unless you have low tolerance or pre existent health issues).Side effects include those of estrogen related (since it aromatizes) and the obvious androgen related ones. All in all, side effects include:AcneHair lossWater retentionHypertensionGynecomastiaAggressionSuppressionNegative effects on lipidsAffects cardiovascular health and othersRemember to use Ment Trest properly if you want to avoid the side effects, because an improper use is almost guaranteeing getting negative side effects.

Definition

Trestolone acetate is a synthetic and injected anabolic–androgenic steroid (AAS) and a derivative of nandrolone (19-nortestosterone) which was never marketed. It is an androgen ester – specifically, the C17 acetate ester of [DB05830].

InChI:InChI=1/C21H30O3/c1-12-10-14-11-15(23)4-5-16(14)17-8-9-21(3)18(20(12)17)6-7-19(21)24-13(2)22/h11-12,16-20H,4-10H2,1-3H3

6157-87-5 Relevant articles

Structure-activity relationship study of human liver microsomes-catalyzed hydrolysis rate of ester prodrugs of MENT by comparative molecular field analysis (CoMFA)

Bursi, Roberta,Grootenhuis, Arijan,Van Der Louw, Jaap,Verhagen, Jos,De Gooyer, Marcel,Jacobs, Peter,Leysen, Dirk

, p. 213 - 220 (2003)

A series of MENT esters (3-71) was desig...

Cp2ZrMeCl: A Reagent for Asymmetric Methyl Addition

Garrec, Kilian,Fletcher, Stephen P.

supporting information, p. 3814 - 3817 (2016/08/16)

The use of Cp2ZrMeCl is described as a s...

Stereoselective synthesis of some methyl-substituted steroid hormones and their in vitro cytotoxic activity against human gastric cancer cell line MGC-803

Li, Chun,Qiu, Wenwei,Yang, Zhengfeng,Luo, Jian,Yang, Fan,Liu, Mingyao,Xie, Juan,Tang, Jie

experimental part, p. 859 - 869 (2010/10/18)

A series of 3-, 7-, 15-, and 16-methyl-s...

PROCESS FOR THE PRODUCTION OF TIBOLONE

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Page 34, (2010/02/08)

Disclosed is a process for the synthesis...

Process for the production of 7alpha-methyl steroids

-

Page 4, (2008/06/13)

This invention relates to a process for ...

6157-87-5 Process route

6-dehydro-19-nortestosterone acetate
2590-41-2

6-dehydro-19-nortestosterone acetate

methylmagnesium chloride
676-58-4

methylmagnesium chloride

7alpha-Methyl-19-nortestosterone acetate
6157-87-5

7alpha-Methyl-19-nortestosterone acetate

Conditions
Conditions Yield
6-dehydro-19-nortestosterone acetate; methylmagnesium chloride; copper diacetate; In tetrahydrofuran; at -45 - -35 ℃; for 3h;
With hydrogenchloride; In tetrahydrofuran; water; at 10 ℃; for 0.5h;
78%
6-dehydro-19-nortestosterone acetate; methylmagnesium chloride; copper(l) chloride; In tetrahydrofuran; at -30 ℃; for 3 - 4h;
With sulfuric acid; water; In tetrahydrofuran; for 1.33333h;
 
zirconocene methyl chloride

zirconocene methyl chloride

6-dehydro-19-nortestosterone acetate
2590-41-2

6-dehydro-19-nortestosterone acetate

7alpha-Methyl-19-nortestosterone acetate
6157-87-5

7alpha-Methyl-19-nortestosterone acetate

Conditions
Conditions Yield
zirconocene methyl chloride; With silver trifluoromethanesulfonate; copper(l) chloride; (3,5-dioxa-4-phospha-cyclohepta[2,1-a;3,4-a']dinaphthalen-4-yl)-bis-(1-phenyl-ethyl)-amine; In diethyl ether; dichloromethane; at 20 ℃; for 0.166667h; Darkness; Inert atmosphere;
6-dehydro-19-nortestosterone acetate; With chloro-trimethyl-silane; In diethyl ether; dichloromethane; at 20 ℃; for 15h; stereoselective reaction; Inert atmosphere; Darkness;
61%

6157-87-5 Upstream products

  • 54793-00-9
    54793-00-9

    17β-hydroxy-7α-methyl-estr-5-en-3-one acetate

  • 3764-87-2
    3764-87-2

    7α-methyl-19-nortestosterone

  • 75-36-5
    75-36-5

    acetyl chloride

  • 434-22-0
    434-22-0

    19-nortestosterone

6157-87-5 Downstream products

  • 15506-01-1
    15506-01-1

    3-methoxy-7α-methylestra-1,3,5(10)-trien-17β-ol

  • 3764-87-2
    3764-87-2

    7α-methyl-19-nortestosterone