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TB-500 5 mg Thymosin Beta 4 Vial - Zyvex Pharmaceuticals

Zyvex Pharmaceuticals

TB-500 5 mg Thymosin Beta 4 Vial - Zyvex Pharmaceuticals

Injection · 5 mg · vial

Out of stock
CompoundThymosin Beta 4
ClassResearch peptide
Half-lifeNot established
Detectionn/a (prohibited, S2)
Liver toxicityLow
Water retentionNone
A synthetic fragment of thymosin beta-4, supplied as a lyophilised powder for reconstitution. Elimination in humans has never been measured, and the vendor material behind this material states that plainly, so the dosing rhythm below is a vendor protocol rather than clinical guidance. The veterinary record shows the LKKTETQ metabolite in horse urine and plasma; the equivalent human detection window is not established. WADA lists thymosin beta-4 and its derivatives in class S2.
TB-500 5 mg Thymosin Beta 4 Vial - Zyvex Pharmaceuticals
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Quality First

All products are manufactured under strict quality standards and independently tested before release. By purchasing, the buyer agrees to use these products in compliance with all applicable laws.

Product Overview

Best Anabolic Steroids lists TB-500 from Zyvex Pharmaceuticals as a lyophilised powder for reconstitution under a single vial, with Thymosin Beta 4 recorded as the active substance. Chemically the vial holds the synthetic fragment of a naturally occurring peptide, and it is catalogued under the short code TB-500 rather than the full protein name. Like every compound on the peptide shelf it arrives as a powder and is mixed with bacteriostatic water at the bench, not sold as a ready-made solution.

The file on this peptide is shorter than most buyers expect. Elimination in humans has never been measured, the sources leave the half-life field empty, and the same sources note that no human dosing, safety or efficacy data have been established. What does exist is veterinary work: the N-acetylated fragment LKKTETQ turned up in horse urine and plasma samples, which is analytical proof that the peptide and its breakdown products are traceable in body fluids, but it says nothing about the human window. The dosing rhythm described further down this page is therefore vendor protocol, not clinical guidance, and the page says so at every step.

Use is concentrated on soft tissue. Community descriptions centre on recovery from training and on joints and connective tissue, and the peptide is normally run as a course with a break afterwards rather than continuously. The peptide next to it in nearly every plan is BPC 157, and the split of labour is well defined: TB-500 is described as the systemic partner while the pentadecapeptide is the one applied locally. GHK-CU 50 covers the skin and collagen end of the same shelf. The three are different molecules with different mechanisms and none of them substitutes for another.

How the Peptide Behaves

The mechanism described in the literature is cell migration and the organisation of actin, which is what a repair peptide does: it moves repair cells to where they are needed rather than signalling growth. The fragment is short, water-soluble and stable in powdered form, and it is the reason the vial can be shipped at ambient temperature and stored for long periods before it is mixed.

Because nothing about the mechanism is hormonal, the peptide does not suppress natural testosterone production and no recovery protocol belongs at the end of a course. What it does require is a cold chain once the powder is dissolved. The reconstituted solution is kept refrigerated, and the sources state no expiry for this particular fill, which is an argument for mixing small volumes and using them promptly rather than preparing a large batch in advance.

The other structural feature worth knowing is the difference from its usual companion. The two peptides act through different routes, and sources who write about them warn explicitly against treating them as interchangeable. Someone planning a repair block picks one as the systemic component and one as the local component, which is why they appear side by side in the protocol cards below rather than as alternatives to one another.

Dosage Protocol

Everything in this table comes from vendor protocol material, not from a clinical trial. No approved dose exists for this peptide and no human pharmacokinetic data support any figure in it.

Phase Amount Frequency Length and notes
Loading 2.0-2.5 mg twice a week Weeks 1-4, a weekly total of 4.0-5.0 mg; at that rate the 5 mg fill lasts about seven days
Maintenance 2.0-2.5 mg once a week Follows loading; the same 5 mg fill then stretches across roughly two and a half weeks
Course length - - 6-8 weeks, then a pause of similar duration before another course
Female None published - The references offer no female schedule for this peptide
Administration Reconstituted solution subcutaneous or intramuscular Volume is worked out from the strength of the solution, never from the size of the vial

The loading step is a vendor convention rather than a measured necessity. With no human half-life to work from, nobody can say how much accumulates during two weekly injections or how quickly the level falls when maintenance starts, and the four week loading window is simply how the reference protocols are written.

Suggested Protocols

These are catalogue patterns. None of the pairings has been studied in humans, and the peptide's own safety record is described in the sources as unestablished.

Systemic partner for a local repair peptide
TB-500 - loading then weekly+BPC 157 - 250-500 mcg daily
6 to 8 weeks, with the pentadecapeptide run at the front of the block when tissue irritation is at its highest. Two mechanisms, one goal, no overlap between them.
Connective tissue and skin
TB-500 - maintenance amounts+GHK-CU 50 - research amounts
4 weeks of overlap. The copper peptide works on collagen synthesis while the fragment works on cell migration, and neither repeats the other's job.
Recovery window inside a training block
8 weeks. The training compounds build and condition; the peptide runs for the first month only, when the tissue load of a new block is heaviest.

What to Expect

  • Weeks 1 to 3. Vendor descriptions place the first change here: less discomfort in the area treated and freer movement in the joints that were bothering the user before the block started.
  • Weeks 3 to 6. The period in which a full course is expected to work, since the reference protocol runs 6 to 8 weeks with loading at the front. Nothing about the timeline has been measured in humans.
  • No hormonal footprint. Testosterone, estrogen and gonadotropins stay where they were. A blood panel is not a way to check whether the peptide is working.
  • The limit. No human half-life, no human dose, no safety profile and no efficacy data have been established. Short courses and one variable at a time are the only controls available.
  • The cold chain. The mixed solution needs refrigeration, and no expiry for this fill appears in the reference material, so preparing it in small volumes matters more than buying in bulk.
  • Testing. Thymosin beta-4 and its derivatives are named in WADA class S2, and the veterinary metabolite data show that the fragments do turn up in urine and plasma samples.

Side Effects and Management

Injection site reactionChange sites each time, keep technique sterile and use a new needle. The most frequently described complaint; human data are limited
Headache or a mild off feelingUser reports mention this; when it lasts more than a day or two, step the amount down and stop for a while. Not independently confirmed
Redness and itching at the siteA cold compress and a pause are usually enough; discard the solution if the reaction repeats on the next injection. Uncommon and local
Cell proliferation concernA theoretical worry for anyone with an oncology history, since the peptide is studied for its effect on cell migration; a clinician rather than a forum should decide. Theoretical, not confirmed
No validated human safety profileThis is the class risk of research peptides: limit the length of a course, keep records and do not stack several unknowns. Not established in sources
Contamination of the mixed vialAlcohol-swab the stopper, never re-use a needle and never return liquid to the vial. Preventable, and the main hazard of home reconstitution

Reconstitution and Storage

Mix the powder with bacteriostatic water and work the strength out from the volume used, never from the number printed on the vial. Fills sold across brands run 2, 5 and 10 mg; the reference protocols use the 5 mg fill because it matches their loading figures, and 5 mg taken up in 2 ml of water gives a 2.5 mg per ml solution, which makes a 2.0 to 2.5 mg dose 0.8 to 1.0 ml of it.

Stage Where it belongs Practical notes
Sealed vial, still dry Cold and dark Leave it cold and out of light until the day it is opened
Mixed solution Refrigerator The reference material gives no expiry for this fill after mixing, which favours small batches over one large one
Every draw Sterile practice Swab the stopper first, use one needle per draw and avoid warming and cooling the solution again and again
Other peptides Separate syringes The sources warn against pulling this peptide into the same syringe as a product whose own instructions forbid mixing

Buying TB-500 by Zyvex Pharmaceuticals

The peptide is listed inside the Zyvex Pharmaceuticals range as a single sealed vial of lyophilised powder. Buyers almost always pair it with BPC 157, and the other repair option on the same shelf is GHK-CU 50, while Ligandrol LGD 4033 and Ibutamoren MK 677 serve the training programmes the peptide usually accompanies. Shipping regions and payment options appear at checkout, parcels are discreet, and questions about the fill of the vial can be settled before the order is finalised.

This page is published as reference material for a research substance. TB-500 from Zyvex Pharmaceuticals is supplied as a research-grade peptide for laboratory work, with no approved indication, no approved dose and no established human safety or pharmacokinetic data. Amounts, phases and reconstitution notes above restate vendor protocol material and are not a prescription. Nothing here should be used to diagnose or treat any condition, and a genuine injury belongs with a qualified clinician. Store the product out of the reach of children and respect the regulations that apply where you live.
Is TB-500 the same thing as thymosin beta-4?
TB-500 is the catalogue name for a synthetic fragment of the naturally occurring peptide thymosin beta-4, and the Zyvex card records Thymosin Beta 4 as the active substance. The fragment carries the active region of the parent peptide, so the vial is a research material built from part of a protein the human body already produces.
Does TB-500 have a human half-life at all?
It has never been established, and the vendor material for this peptide says so directly rather than quoting a figure. That is why the loading and maintenance rhythm on this page is presented as vendor protocol: with no measured clearance, nobody can tell you how fast a level builds or falls.
How is TB-500 dosed, and what does the loading phase look like?
Reference protocols load for the first four weeks at 2.0 to 2.5 mg twice a week, a weekly total of 4.0 to 5.0 mg, then step down to 2.0 to 2.5 mg once a week. At those rates the 5 mg fill is used up in about seven days of loading and stretches across roughly two and a half weeks in maintenance. None of it comes from a clinical study.
How long does a TB-500 course last?
Six to eight weeks is the vendor figure, then a pause of similar length before another course. That rhythm is a convention rather than a measured optimum, since no human study has compared different course lengths or established what a safe repeat interval would be.
How do you reconstitute a TB-500 vial and how do you read a dose?
Add bacteriostatic water and calculate the concentration from the volume, not the vial size. A 5 mg vial with 2 ml of solvent gives 2.5 mg per ml, so a 2.0 to 2.5 mg dose is 0.8 to 1.0 ml. The mixed solution is refrigerated, and the exact shelf life for this vial is not confirmed in the sources.
How quickly do people notice anything from TB-500?
Vendor descriptions place the first change in comfort and movement one to three weeks in, with the full course running 6 to 8 weeks. Those timelines are vendor material, not study results, and because no human half-life or efficacy data exist they cannot be checked against anything. Compare that with BPC 157, which is normally applied locally.
Is TB-500 banned in sport?
Yes. Thymosin beta-4 and its derivatives, TB-500 included, are named in WADA class S2, so the peptide is prohibited. Analytical work in horses found the N-acetylated metabolite LKKTETQ in urine and plasma, which shows the fragments are traceable in body fluids even though no human detection window has been set.
Does TB-500 need PCT, and has it been tested in humans?
No post-cycle therapy is required, because the peptide does not suppress gonadotropin signalling; between courses the vendor advice is simply a break of similar length. On human testing, the honest answer is that no established human dosing, safety or efficacy data exist, so there are no laboratory markers that could be used to follow the course.

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