Purity vs quantity distinction
Purity (%) and reported quantity are distinct analytical parameters. Review purity and reported quantity separately, and confirm the labeling and assay basis for the batch proposed for your order.
NAD+ 500mg Vial
A 500mg per-vial fill specification treated as a high-fill project specification, supplied under qualified B2B technical evaluation.
High-fill 500mgMoisture controlPackaging protectionStorage documentationB2B sourcing
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. Protective outer packing appropriate to a high-fill 500mg vial; NAD+ is hygroscopic, so vials should stay sealed until use. 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 peptide sourcing, chromatographic purity and delivered quantity require separate evaluation. We keep purity and labeling basis distinct on available documentation, so buyers can review analytical parameters for their quoted batch before ordering.
Batch-specific documents
Batch documentation reflects the specific lot produced. Ask which batch-specific documents are available for the quoted lot, including COA and supporting HPLC or MS records where applicable.
Documented before commitment
Ingredient identity (INCI / CAS), specification sheet, and SDS are available for technical review. Confirm documentation for the batch proposed for your order before purchase.
Documents Available
Documents Available
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
B2B Review Guide
B2B Review Guide
Product Overview
This page outlines the review fields for a high-fill NAD+ sourcing discussion from a B2B procurement perspective.
What WUMO Can Supply
- 500mg NAD+ lyophilized vial fill specification
- Batch-specific COA available under documentation review
- Packaging protection discussion
- Moisture content records
- Storage condition documentation
- Shipping and receiving condition review checklist
Quality and Documentation
Standard NAD+ documentation review scope includes identity records, HPLC purity records, appearance records, water content records, and packaging protection 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
What does the 500mg fill specification mean from a sourcing perspective?
It is a vial fill quantity and B2B project specification. It is not a use amount.
Why does a 500mg fill require more packaging review?
A 500mg per-vial fill is treated as a high-fill project specification and may require more attention to moisture management, barrier layer specification, and shipping condition.
What packaging protection options are available?
Outer packaging, barrier layers, and desiccant inclusion are discussed on a project basis. Specific configurations are subject to project confirmation.
What documentation can be shared under B2B technical evaluation?
Batch-specific COA, identity records, HPLC purity records, water content records, and packaging protection 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.
- NAD+ 500mg high-fill vial planning — what a high fill changes for OEM and distributor projects.
- What a 10mg vial actually contains — how peptide content, counterion, moisture and excipients divide up the mass, and what a per-vial claim needs behind it.
- Lyophilized cake appearance and reconstitution — why cakes hold or collapse, what the excipient system does, and what can reasonably be specified.
OEM / Private Label
Want NAD+ 500mg 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.