TURIPEX 10

$135.00

Pack

100 Tablets x 10mg.

Half Life

16 hours

Dosage

Men 20-50 mg/day

Acne

Yes

Water Retention

Low

HBR

Perhaps

Aromatization

No

Hepatotoxity

Yes

Chemical Name: 4-Chlorodehydromethyltestosterone
Chem.Abstr.Name: 4-chloro-17b-hydroxy-17a-methyl-androst-1,4-dien-3-one
Molecular Structure: C20H27O2Cl
Molecular Weight: 334.8854

Oral Turinabol Overview

Oral Turinabol is a unique anabolic steroid with a distinct structure and history. It was developed as a hybrid between Methandrostenolone (Dianabol) and Clostebol, combining strong anabolic properties with reduced androgenic activity.

The compound was first introduced in 1962 by Jenapharm in East Germany. For many years, it maintained a reputation for safety in medical use.

Therapeutic background:

  • Used in men, women, and even children

  • Helped preserve lean muscle mass

  • Supported bone density

  • Delivered results with relatively low complication rates

However, its reputation changed in the 1990s when the East German doping program became public. Between 1974 and 1989, the government systematically administered steroids, including Oral Turinabol, to Olympic athletes.

Historical significance:

  • Central compound in the East German doping program

  • Undetectable in drug testing at the time

  • Used alongside epitestosterone to mask testosterone levels

  • Discontinued by Jenapharm in 1994

  • Never reintroduced by Schering after acquisition

  • Now exists only through underground production

Since its discontinuation, it has never returned as a legitimate pharmaceutical product.


Oral Turinabol Functions & Traits

Oral Turinabol (4-chlorodehydromethyltestosterone) is structurally related to Dianabol, which itself is derived from testosterone.

Structural modifications:

  • Double bond at carbon 1 and 2 improves anabolic ratio

  • Chlorine group at carbon 4 prevents aromatization

  • Methyl group at carbon 17 allows oral use (C17-aa classification)

Functional traits:

  • Enhances protein synthesis

  • Improves nitrogen retention

  • Increases red blood cell count

  • Supports muscular endurance

  • Promotes faster recovery

While these anabolic properties are present, they are milder compared to stronger bulking steroids. The benefit lies in cleaner, steadier progress without estrogen-related side effects.

Additional important trait:

  • Reduces Sex Hormone Binding Globulin (SHBG)

  • Increases free, active testosterone levels

  • Enhances effectiveness of other steroids in a stack

  • Improves overall synergy without raising total dosage

This SHBG-lowering ability makes it particularly valuable in combination cycles.


Effects of Oral Turinabol

Oral Turinabol shines most in true athletic performance enhancement rather than bodybuilding mass cycles.

Athletic advantages:

  • Noticeable increase in endurance

  • Improved recovery between sessions

  • Greater strength output

  • Enhanced power and speed

  • Reduced seasonal physical wear and tear

It does not create athletic skill but enhances existing performance capacity. Its long-term success in competitive sports demonstrates its effectiveness.

Off-season bulking use:

  • Moderate lean muscle gains

  • No water retention

  • Clean, dry weight increases

  • Less dramatic mass compared to Dianabol or Anadrol

  • Gains consist primarily of lean tissue

Due to SHBG reduction, it may also enhance the effectiveness of compounds like Deca Durabolin during bulking phases.

Cutting phase use:

  • Strong lean tissue protection

  • Improved muscular endurance

  • Increased recovery in calorie deficit

  • Moderate increase in muscle hardness

Hardening effect is present but milder than compounds like Winstrol, Masteron, or Trenbolone. Many athletes use it early in a cutting phase before transitioning to stronger hardening agents later.


Side Effects of Oral Turinabol

Oral Turinabol is considered one of the milder anabolic steroids overall, but it is not risk-free. Cardiovascular strain is the primary concern.

Estrogenic

  • Does not aromatize

  • No progestin-related activity

  • No gynecomastia risk

  • No water retention

  • Lower risk of blood pressure spikes from fluid retention

Androgenic

  • Very low androgenic activity

  • Acne possible (rare)

  • Hair loss possible in predisposed individuals

  • Body hair growth possible

  • Not significantly affected by 5-alpha reductase inhibitors

Female use considerations:

  • Low doses may avoid virilization

  • High doses increase risk

  • Possible symptoms: deepened voice, body hair growth, clitoral enlargement

  • Discontinue immediately if symptoms appear

Women do not require exogenous testosterone support.

Cardiovascular

  • Increases LDL (bad cholesterol)

  • Decreases HDL (good cholesterol)

  • Greater cholesterol impact than most injectables

  • Moderate-to-strong oral impact

Risk management:

  • Avoid use if already prone to cholesterol issues

  • Maintain low saturated fat intake

  • Limit simple sugars

  • Increase omega fatty acid intake

  • Supplement with fish oil

  • Consider cholesterol-support antioxidants

  • Include consistent cardiovascular exercise

Testosterone Suppression

  • Suppresses natural testosterone production

  • Exogenous testosterone recommended for men

  • Risk of low testosterone symptoms without support

Post-cycle considerations:

  • Natural production resumes slowly

  • PCT strongly recommended

  • Helps prevent cortisol dominance

  • Protects lean muscle during recovery

  • Speeds up hormonal normalization

PCT improves recovery but does not instantly restore natural levels.

Hepatotoxicity

  • Classified as C17-aa

  • Causes liver enzyme elevation

  • Stress indicator, not automatic damage

  • Moderate hepatotoxicity

Liver protection guidelines:

  • Avoid use if pre-existing liver issues exist

  • Eliminate or severely limit alcohol

  • Avoid unnecessary OTC medications

  • Use liver support supplements

  • Monitor enzyme levels

When used responsibly and with a healthy liver, enzyme values should return to normal after discontinuation.

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