SS-31 50mg Vial

A 50mg vial fill specification for SS-31, supplied under qualified B2B technical evaluation with batch-linked HPLC purity and ESI-MS identity records, batch consistency, and lead time planning support.

Category
Lyophilized Peptides
SS-3150mg vial fillTechnical procurementIdentity documentationBatch documentation

Review specifications, files, and next-step support before requesting samples.

  • Confirm the peptide name, CAS, and core specifications
  • Check typical applications and document availability
  • Use one inquiry path for pricing, files, samples, or project discussion

Key Review Snapshot

Key Review Snapshot

Start with the review points that shape quotation quality.These checkpoints help buyers align file scope, vial format, packaging, MOQ, lead time, and buyer-side review before comparing supplier offers.
Product FormatLyophilized peptide vial
Supply FocusB2B sourcing and documentation review
DocumentationBatch COA stating RP-HPLC purity and MS identity, plus SDS/MSDS and specification sheet. Karl Fischer water content and counter-ion data are arranged per project where a specification requires them.
Quotation ScopeFill amount, vial count, packaging format, MOQ, and lead time are confirmed together at quotation stage.
PackagingSealed lyophilized vial with stopper and cap. Neutral-label or private-label discussion for qualified projects. Store unopened vials at 2–8 °C as standard, or −20 °C for long-term storage — approximately 24 and 36 months respectively as WUMO product guidance, with the batch COA and product documentation governing. Keep sealed, protected from light and moisture.
ComplianceBuyer-side market review required

Why buyers trust WUMO

Real content, documented — not guesswork

In this market, “99% pure” is often quoted while the amount actually delivered is far less. We keep purity and real content separate, and put both on paper — so SS-31 50mg Vial is backed by documents you can check.

Research peptide line — typical purity >99.3–99.4%, every batch MS-checked before release.

Content equals the label

Purity (%) and content (the actual amount delivered) are not the same thing. We document both, so the amount on the label is the amount you receive — no quiet shortfalls.

Every batch is verified

Identity and quality are confirmed by batch documentation — COA, plus HPLC / MS where applicable — before material is released.

Documented and traceable

Ingredient identity (INCI / CAS), specification sheet and SDS are available for review. Match the documents to your quoted batch before you commit.

Documents Available

Documents Available

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COA

Batch-specific COA

Batch-level quality summary for buyer-side file review.

Request this file through the inquiry path below.

HPLC

HPLC Report

Purity profile reference for the quoted project or batch where available.

Request this file through the inquiry path below.

MS

MS / Identity Records

Request scope and availability through the B2B inquiry path.

Request this file through the inquiry path below.

SDS

SDS/MSDS

Safety document requested for internal purchasing and handling review.

Request this file through the inquiry path below.

Overview

Overview

SS-31 is, from a sourcing standpoint, a synthetically demanding peptide. Synthesis route, batch-level identity verification, and purity documentation typically receive more procurement-side attention than less complex peptide sourcing projects. This page does not describe biological action, end-user application, or product performance.

B2B Review Guide

B2B Review Guide

Product Overview

A 50mg lyophilized vial fill is the specification supplied on this page. Documentation review takes place under qualified B2B technical evaluation.

Batch Analytical Record

The most recent SS-31 batch was analysed on 21 July 2026. Both records below are supplier-side quality control performed in the production laboratory — they are not third-party verification. The two are complementary rather than interchangeable, and buyers who need independent confirmation can arrange it where authorised.

Measurement Result Method and date
Purity (RP-HPLC) 99.59% by area Agilent 1260, UV 220 nm, single injection report, 21 July 2026
Identity (ESI-MS) [M+H]⁺ 640.72; [M+2H]²⁺ 320.93 Waters ZQ2000, electrospray positive mode, 21 July 2026
Molecular weight 639.79 Both observed charge states convert back to this same weight

Identity here rests on agreement between two charge states rather than a single peak match: the singly and doubly charged ions independently return the same molecular weight. Purity is an area-percent figure at 220 nm and is a separate question from content or assay — how clean the material is, not how much peptide is in the vial. The chromatographic integration on this report is annotated as manual integration, which is disclosed on the report itself and can be discussed on request.

Figures above describe the analysed batch. The batch identifier, retest date, and any batch-to-batch variation are confirmed on the batch-specific COA supplied with a quotation. For background on how identity, purity, and content differ, see how peptide identity is confirmed by mass spectrometry.

What WUMO Can Supply

  • 50mg SS-31 lyophilized vial fill specification
  • Batch-specific COA available under documentation review
  • Purity and identity records
  • Batch consistency records subject to project confirmation
  • Lead time planning discussion
  • Controlled or cold-chain shipping discussion where applicable

Quality and Documentation

Documentation that a technical procurement team reviewing SS-31 typically requests includes identity records, HPLC purity records, water content, appearance records, and counter-ion form records. Specific values are subject to batch-specific COA and project confirmation.

Compliance Note

This page is for qualified B2B technical evaluation and business-side documentation review only. This page is not intended for individual purchase, consumer use, or product-use guidance. Final use, importation, labeling, and local compliance are the buyer's responsibility.

FAQ

Why is SS-31 described as a synthetically demanding peptide?

From a sourcing standpoint, SS-31 synthesis carries higher procurement-side requirements around batch consistency and identity verification than standard peptides. This page describes that sourcing-side reality.

What does the 50mg fill specification refer to?

A 50mg vial fill quantity, supplied as a B2B project specification. It is not a use amount.

Why might SS-31 lead time be longer than for other peptides?

Synthesis complexity and batch-level documentation requirements can extend production timelines. Exact lead time ranges are subject to project confirmation.

Does WUMO offer controlled or cold-chain shipping for SS-31?

Controlled or cold-chain shipping options are discussed on a project basis, depending on destination, transit time, and packaging plan.

What documentation can be shared during B2B technical evaluation?

Batch-specific COA, identity records, HPLC purity records, water content records, and counter-ion form records, with scope subject to project confirmation.

Specification and documentation references

Before requesting a quotation, these guides cover the specification and document questions that come up most often on this product.

OEM / Private Label

Want SS-31 50mg Vial under your own brand?

For finished lyophilized peptide vials with custom labels and packaging -- covering MOQ, sample or pilot evaluation, and batch documentation such as COA, sterility, and endotoxin reports -- see our private label peptide vial (OEM / ODM) service.

Request Pricing, Files, or Samples

Use this form for pricing, technical files, sample requests, or project discussion for this product.

Need COA, SDS/MSDS, or specifications? Choose "Technical document request" in the inquiry form or mention the file name in your message.