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SS-31 supplied as lyophilised powder in a multi-dose vial with matching injector pen, unbranded for private label

Longevity

SS-31

CoA per batch HPLC >=98% Private label available Laboratory and research use

SS-31, also written SS 31, is supplied by White Label Peptides as a lyophilised powder in multi-dose vials, for laboratory and research use, to business buyers only. It sits in our longevity category. Every batch is verified by HPLC and ships with its own Certificate of Analysis.

CompoundSS-31
Also known asElamipretide
SynonymsElamipretide
ClassificationMitochondrial Function & Cellular Energy Research Peptide
Peptide typeMitochondrial-Targeted Tetrapeptide
Molecular formulaC32H49N9O5
Molecular weightApproximately 639.8 g/mol
SequenceD-Arg-dimethylTyr-Lys-Phe-NH2
FormLyophilised peptide powder - Multi-dose research vials - Injectable research format
AppearanceWhite to off-white lyophilised powder prior to reconstitution
PresentationVials: 10 mg
ReconstitutionTypically reconstituted using: Bacteriostatic water - Sterile laboratory-grade water
StorageStore refrigerated at 2-8°C in a cool, dry environment away from direct sunlight. Long-term storage may require freezing conditions prior to reconstitution.

Specification data is provided for identification and procurement. It is not dosing guidance and it is not a claim of any effect.

Evidence and status

Approval statusApproved, as elamipretide. FORZINITY injection, NDA 215244, accelerated approval September 2025, Stealth BioTherapeutics. Indicated to improve muscle strength in adult and paediatric patients with Barth syndrome weighing at least 30 kg
European statusNo European authorisation identified in this review
Strongest supportApproved label, accelerated approval on an intermediate endpoint
Route contextInjection, per the approved label
Competitive sportNot checked against the 2026 List by name here. Note that S0 no longer reaches it: S0 covers substances with no approval from any governmental regulatory health authority, and since September 2025 this molecule has one. Verify with the relevant anti-doping organisation
  1. Lab work
  2. Animal studies
  3. Human studies
  4. Approved label

Reviewed 2026-09-02. Regulatory status is stated for procurement and varies by market. It is not legal advice.

Research

What the published literature examined

The molecule went through a full regulatory programme in one narrow indication. FDA brought the application to the Cardiovascular and Renal Drugs Advisory Committee on 10 October 2024 and granted accelerated approval in September 2025, the first approval for Barth syndrome, an ultra-rare genetic disorder. The approval rests on knee extensor muscle strength measured by hand-held dynamometry, used as an intermediate clinical endpoint rather than as a demonstration of clinical benefit. A confirmatory randomised trial is running as a condition of that approval.

What is not established

Confirmed clinical benefit, which is precisely what accelerated approval defers. The endpoint the approval rests on is an intermediate one, and the trial required to confirm benefit is still running. There is no approval for anyone under 30 kg. And nothing in the approval addresses any use outside Barth syndrome: the regulatory record establishes an effect on muscle strength in one ultra-rare mitochondrial disorder, and establishes nothing about the mitochondrial and longevity uses this compound is generally sold for.

What distinguishes SS-31

It is the newest approval in this catalogue and by far the narrowest, and the gap between those two facts is the whole point. Sellers of SS-31 rarely mention that the molecule is now an approved drug; the ones who do rarely mention that the approval covers an ultra-rare genetic disorder, in patients over 30 kg, on an intermediate endpoint, with benefit still to be confirmed. An approval is a fact about one indication and one population, not a general endorsement of a molecule, and this compound is the clearest example of that distinction in the range.

Sources

  1. US FDA. FDA grants accelerated approval to first treatment for Barth syndrome, September 2025
  2. US FDA. NDA 215244 accelerated approval letter, Stealth BioTherapeutics Inc.
  3. US FDA. Briefing document, NDA 215244, Cardiovascular and Renal Drugs Advisory Committee, 10 October 2024
  4. US FDA. NDA 215244 integrated review
  5. ClinicalTrials.gov. NCT07531251, 4TAZPower, clinical trial in patients with Barth syndrome

This page describes a compound as a material and summarises published research about it. It is for general and procurement information only. It is not medical advice, not a treatment recommendation, and not guidance on use. Supplied for laboratory and research use, not for human consumption.

Specification

About this compound

The specification below is the batch-independent data. Purity and analysis date vary by batch, so they appear on the certificate issued with your order rather than on this page.

What this compound is

SS-31 in supply terms

SS-31, also supplied under the name Elamipretide, is a synthetic tetrapeptide with the sequence D-Arg-dimethylTyr-Lys-Phe-NH2. Two features distinguish its chemistry from a standard amino acid chain: a D-amino acid at the first position, which resists the enzymes that break down conventional L-amino acid peptides, and a C-terminal amide cap in place of a free carboxylic acid. The molecular formula is C32H49N9O5, with a molecular weight near 639.8 g/mol. The site lists it as a mitochondrial-targeted tetrapeptide, a category label describing the class of short, charge-modified peptides grouped together on this catalogue rather than a claim about the compound. It is supplied as a lyophilised powder in multi-dose vials at a 50mg fill weight, in an injectable research format, and reconstitutes with bacteriostatic water or sterile laboratory-grade water. Storage is 2-8C, out of direct sunlight, with freezing suitable for extended holding before reconstitution. Because SS-31 is one of the smaller-formula peptides in this catalogue by molecular weight, buyers should check whether a quoted price reflects the 50mg vial fill directly or an unspecified concentration, and confirm HPLC purity data accompanies each batch on the Certificate of Analysis.

This section describes the compound as a material. It makes no claim about any effect and is not guidance on use.

What varies by batch

The page identifies the compound. The certificate records the batch.

Purity, method, analysis date and issuing party belong on the batch record rather than in page copy.

Send the volume you need for SS-31 and your delivery country. We will quote against it.Request pricing

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Questions

Supply, answered

Is SS-31 available for private label?

Yes. It can be supplied under your own brand on the vial and the carton, with the Certificate of Analysis issued under your product name.

What is the minimum order quantity?

Set for this compound specifically and confirmed at the enquiry stage, before you commit.

What purity is supplied?

98 percent or higher, verified by HPLC. The certificate issued with your batch carries the actual figure for that batch.

How is it shipped?

As lyophilised powder in multi-dose vials, packed for transit. Delivery in 5 to 7 days once the batch is released.

We already buy SS-31. Can you quote against our current volume?

Yes. Send the volume and the delivery country. Pricing is tiered per compound, so the quote reflects what you buy rather than a list price.

Can you supply SS-31 as a second source?

Yes. Terms are agreed per compound, so you can add SS-31 without moving anything else you buy elsewhere.

Request pricing for SS-31

Indicative volume and delivery country is enough to start. We reply within one working day.

Anything else you already know. All optional.

We supply businesses across Europe, and we reply within one working day.