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Lexicon

Stanozolol Water - Research Substance

Aqueous suspension of stanozolol for intramuscular injection in research contexts.

2 min read 8 sources

Glass vial with the black TPD label and a blue cap on a white podium, next to it a blue 3D steroid molecule, symbolic image for Stanozolol Water
Formerly approved · from 1962 as a tablet, now off the market

Summary

At a glance

Sources checked on 25 Oct 2026

HDL cholesterol in 6 weeks
-33 %

Stanozolol as a tablet in 11 weight lifters, only -9% with testosterone injections3

LDL cholesterol
+29 %

Same trial, LDL fell by 16% with testosterone3

Binding to the androgen receptor
<5 %

Relative to the reference androgen methyltrienolone, muscle and prostate in animal models4

Trial with the injection in water
12 men

Single injection into the muscle: fibrinolysis rose, HDL fell after one month1

Side effects in long-term treatment
18 of 37

Tablets for hereditary angioedema, mostly raised liver values, reversible at a lower dose5

  • Stanozolol Water is stanozolol as a suspension in water for injection into the muscle. The compound is a 17-alpha-alkylated steroid from the DHT family that targets the androgen receptor.81
  • In binding assays stanozolol held only weakly to the androgen receptor, clearly weaker than testosterone or nandrolone.4
  • The clearest human finding concerns blood lipids: as a tablet stanozolol lowered HDL by 33 percent in 6 weeks and raised LDL by 29 percent. HDL also fell after a single injection.31
  • In long-term treatment with tablets raised liver values were the most common side effect. A case report describes severe cholestasis after two months of injections.52
  • According to ChEMBL stanozolol has been an approved drug since 1962, clinically as a tablet. Everything here is the state of research, not a recommendation.8
Profile

Updated June 2026

How long does it stay in the body?

Share left after one dose, calculated with a half-life of ~7 hours

Half-life ~7 hours
After 14 hours: 25 %
Hour 7 · 50 %Hour 14 · 25 %Hour 21 · 12.5 %Hour 35 · 3.1 %

Simplified model without an absorption phase, half-life from the TPD lexicon. The lexicon gives 6 to 8 hours, we calculate with the middle.

Class
DHT-derived synthetic anabolic steroid
Use
Research substance

aqueous formulation

Half-life
Approx. 6-8 hours

faster than oil

Status
WADA banned

not for human administration

Sizes
50mg/ml

1 size in the shop

Contents 13 sections
  1. At a glance
  2. What is Stanozolol Water?
  3. How it works
  4. Use and dosing
  5. What the research shows
  6. Research status
  7. Side effects
  8. Storage
  9. PCT / after coming off
  10. Related compounds
  11. FAQ
  12. Glossary
  13. Sources

What is Stanozolol Water?

Stanozolol Water is a sterile aqueous suspension solution of stanozolol for intramuscular injection. This form is highly concentrated (100 mg/ml) and is commonly used in research contexts. Since the drug is suspended in water (not dissolved), the solution must be shaken before each injection to ensure uniform concentration.

This information is for research and educational purposes only. No medical advice.

Comparison

Three forms of stanozolol

The same compound at the same receptor as a tablet, oil solution or water suspension, as stated in the TPD lexicon. Tap a card to open its entry.

Simplified: the form changes how fast stanozolol reaches the blood. At the receptor it is always the same compound. 8

How it works

Stanozolol binds to the androgen receptor and promotes protein synthesis and nitrogen retention. The aqueous suspension is absorbed faster than oil solutions, leading to faster blood level peaks.

  • DHT-like androgen receptor agonist activity
  • Rapid absorption and higher blood level variability
  • Weakly aromatizable
  • Promotes dry muscle gain

Where it acts

Where stanozolol acted in studies

Tap a point or a card. Red = androgen receptor, grey = observed in studies.

  1. Skeletal muscle

    Binds to the androgen receptor, clearly weaker than testosterone in assays4

    AR
  2. Blood lipids

    HDL fell and LDL rose, as a tablet more than with testosterone3

    Observed in trials
  3. Liver

    Raised liver values as the most common side effect of long-term treatment5

    Observed in trials
  4. Skin and hair

    Acne and increased hair growth in long-term treatment6

    Observed in trials

Targets in the ChEMBL database8

Compound CHEMBL2079587: one recorded mechanism, agonist with direct binding to the human receptor.

Androgen receptor
Gene
AR
UniProt
P10275
ChEMBL
CHEMBL1871
Action
Agonist, direct binding
Blue 3D molecules streaming through a glass tube into a bundle of translucent fibres, suggested muscle fibres
Stanozolol reaches the muscle through the blood and binds to the androgen receptor there. Symbolic image.

Use and dosing

Dosing

Dosing, titration and syringe

Loading the dosing information …

  • Getting started and stepping up, drawn as a staircase
  • Units on the U-100 syringe for every step
  • How long one vial lasts
Glass vial with milky white suspension, a blue cap and a black TPD label for Stanozolol Water, a disposable syringe beside it
Aqueous suspension, given once intramuscularly in studies. Symbolic image.

What the research shows

Stanozolol suspension shows similar effects to the oil formulation but with faster absorption. This results in greater blood level variability with peaks and troughs. Research indicates strong anabolic effects but also significant lipid dysregulation.

  • Faster absorption than oil solution
  • Greater blood level variability
  • Similar anabolic and androgenic effects
  • Suspension particles can cause local irritation

Study results

What the trials measured

Interactive: switch tabs, tap points, show or hide arms. Arms are named relative to each other, no dosing advice.

Blood lipids head to head3

Change in percent, 11 weight lifters, each received both agents in turn

HDL cholesterol3
Stanozolol (tablet, daily) -33%
Testosterone Enanthate (injection, weekly) -9%
HDL2 subfraction3 No figure for testosterone in the abstract
Stanozolol (tablet, daily) -71%
Apolipoprotein A-I3
Stanozolol (tablet, daily) -40%
Testosterone Enanthate (injection, weekly) -8%
LDL cholesterol3
Stanozolol (tablet, daily) +29%
Testosterone Enanthate (injection, weekly) -16%
Hepatic lipase3 Not significant with testosterone
Stanozolol (tablet, daily) +123%
Testosterone Enanthate (injection, weekly) +25%

Values from the trial abstract. Stanozolol was given as a tablet here, the authors attribute the strong effect on HDL to oral use of a 17-alpha-alkylated steroid. After a single injection of stanozolol in water HDL also fell while LDL rose (no percentages in the abstract).

Glass model of a branching blood vessel with a yellow deposit in a display case on a white plinth
The clearest human finding concerns blood lipids: HDL fell and LDL rose. Symbolic image.

Research status

Where the research stands

ClinicalTrials.gov lists only one trial with stanozolol: tablets together with another agent in a blood disorder, status unknown. It is not listed here. As of 25 Oct 2026. 7

  1. Preclinical Binding assays on receptors from rats and rabbits
  2. Phase 1 no registered trial
  3. Phase 2 no registered trial
  4. Phase 3 no registered trial
  5. Approval from 1962 as a tablet, now off the market
Approved: ChEMBL lists stanozolol with phase 4 as the highest phase and first approval in 1962. Clinically it was given as a tablet.8

The approval predates today's trial registries, so the register shows no current trial for this form. 7

Side effects

The aqueous suspension has similar systemic side effects as the oil formulation but may produce stronger peak effects due to higher blood level variability:

  • Hepatotoxicity (C-17 alkylated)
  • Lipid dysregulation (HDL decrease, LDL increase)
  • Local injection pain (aqueous suspension is irritating)
  • HPTA suppression
  • Androgenization effects
  • Joint pain despite muscle gain

Tolerability

Long-term treatment with tablets

Out of 100 people treated for hereditary angioedema: how many had the event, converted from the case numbers of two long-term reports.

49 of 100 Stanozolol tablets over years
Event Stanozolol tablets over years
Side effect until the lowest effective dose5 49%
Complaints over 20 to 40 years6 48%
Low HDL6 24%
High triglycerides6 10%

18 of 37 treated people (mainly raised liver values plus increased hair growth and menstrual changes) as well as 10, 5 and 2 of 21 treated people. Every side effect subsided at a lower dose, the long-term group showed no persistently raised liver values.56

Storage

Stanozolol Water should be stored at room temperature in a dark container. It must not be frozen as this will damage the suspension. Always shake before use.

  • Room temperature (15-25°C)
  • Protected from light and heat
  • Do not freeze
  • Shake thoroughly before each use

Related

Related compounds

Same receptors or blends with Stanozolol Water - Research Substance: all in the TPD lexicon.

FAQ

Common questions about Stanozolol Water - Research Substance

Short answers, each backed by the sources below.

How does Stanozolol Water differ from the tablet?

The compound is the same. In Stanozolol Water it floats as fine particles in water and is injected into the muscle, so the vial has to be shaken before every draw. Clinically stanozolol was given as a tablet. For the injection in water there is one small trial with a single dose.81

Is stanozolol approved?

The ChEMBL database lists stanozolol as an approved drug with first approval in 1962. Long-term reports describe treating hereditary angioedema with tablets over decades. ClinicalTrials.gov lists only a single trial with stanozolol (as of 25 October 2026).867

What happens to blood lipids?

In a trial with 11 weight lifters stanozolol as a tablet lowered HDL by 33 percent in 6 weeks and the HDL2 subfraction by 71 percent. LDL rose by 29 percent. With testosterone injections HDL fell by only 9 percent. After a single injection of 50 mg stanozolol in water HDL also fell in 12 healthy men after one month while total and LDL cholesterol rose.31

How strongly does stanozolol bind to the androgen receptor?

Weakly. In a comparison of several anabolic steroids on receptors from rat and rabbit muscle and prostate stanozolol's binding was below 5 percent of the reference androgen. Nandrolone and testosterone bound much more strongly. ChEMBL still lists stanozolol as an agonist at the androgen receptor.48

How does stanozolol affect the liver?

Stanozolol is 17-alpha-alkylated. In long-term treatment with tablets raised liver values were the most common side effect and subsided at a lower dose. A case report describes a 19-year-old who injected stanozolol for two months: severe cholestasis with liver failure. His liver values only returned to normal five months after stopping.52

What did the trial with the injection in water show?

Twelve healthy men received a single dose of 50 mg stanozolol into the muscle. From 24 hours plasminogen activator rose and stayed raised for a week, plasminogen rose from day two for three weeks. This points to stronger fibrinolysis. After one month HDL had fallen while total and LDL cholesterol had risen.1

Which side effects showed up over years?

Of 21 people with hereditary angioedema who took stanozolol tablets for 20 to 40 years, 10 had complaints: increased hair growth, weight gain, menstrual changes, acne and mood swings. Five had low HDL, two had raised triglycerides. The complaints subsided at a lower dose.6

Glossary

Terms explained briefly

Dotted words in the text open these explanations directly.

17-alpha alkylation
A methyl group on carbon 17 protects the steroid from breakdown in the liver. It stays active as a tablet but puts more strain on the liver.
Androgen receptor
Protein inside the cell that testosterone and related steroids bind to. It then switches on genes for muscle growth and male traits.
Fibrinolysis
Breakdown of blood clots by the body's own enzymes such as plasmin.
HDL
High-density lipoprotein, the so-called good cholesterol. It carries cholesterol from the vessels back to the liver.
Hepatotoxicity
Harmful effect on the liver, first visible as raised liver values in the blood.
Hereditary angioedema
Inherited condition with recurring swelling of skin, gut or airways. Attenuated androgens such as stanozolol were used against it.
HPTA
Hypothalamic-pituitary-testicular axis: the control loop of the body's own testosterone production. Androgens from outside slow it down.
Intramuscular
Injected into the muscle, not under the skin.
LDL
Low-density lipoprotein. High levels count as a risk for deposits in the vessels.
Nitrogen retention
The body excretes less nitrogen than it takes in. This counts as a sign of protein build-up.
Suspension
Solid particles float in a liquid without dissolving. They settle, which is why the vial is shaken before drawing.

Practice

PCT / after coming off

Anabolic substances suppress the body's own testosterone production in the research context. Anyone who comes off a cycle (rather than running it continuously) typically uses a post-cycle therapy (PCT) to restart the natural axis (HPTA).

The standard scheme in the research/literature context combines a SERM (tamoxifen and/or clomifene, alternatively enclomiphene) over roughly four weeks, optionally preceded by HCG to re-sensitise the testes before the SERM block. An aromatase inhibitor (anastrozole/exemestane) belongs more to on-cycle estrogen control than to the PCT itself.

Tip: order the PCT items together with the cycle so they are already on hand when you come off.

This information serves research and educational purposes only. Not medical advice.

Evidence

Sources

Show all 8 sourcesHide sources 6 Studies1 Trial registry1 Database checked 25 Oct 2026

Studies

  1. Single injection: fibrinolysis and blood lipids in healthy men

    Small et al., Thrombosis Research, 1982

    Checked 25 Oct 2026 via doi.org, Crossref, PubMed
  2. Case report: severe cholestasis and liver failure

    Stępień et al., Clinical and Experimental Hepatology, 2015

    Checked 25 Oct 2026 via doi.org, Crossref, PubMed
  3. Blood lipids with stanozolol compared with testosterone

    Thompson et al., JAMA, 1989

    Checked 25 Oct 2026 via doi.org, Crossref, PubMed
  4. Binding of anabolic steroids to the androgen receptor in muscle and prostate

    Saartok et al., Endocrinology, 1984

    Checked 25 Oct 2026 via doi.org, Crossref, PubMed
  5. Ten years of treating hereditary angioedema with stanozolol

    Sheffer et al., Journal of Allergy and Clinical Immunology, 1987

    Checked 25 Oct 2026 via doi.org, Crossref, PubMed
  6. Safety of long-term treatment over 20 to 40 years

    Sloane et al., Journal of Allergy and Clinical Immunology, 2007

    Checked 25 Oct 2026 via doi.org, Crossref, PubMed

Trial registry

  1. Trials on ClinicalTrials.gov

    ClinicalTrials.gov, U.S. National Library of Medicine

    Checked 25 Oct 2026 via ClinicalTrials.gov API v2

Database

  1. Mechanism and approval in ChEMBL

    ChEMBL, EMBL-EBI (CHEMBL2079587)

    Checked 25 Oct 2026 via ChEMBL

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