Attest214
Now accepting lots · Onboarding beta

A certificate you cannot edit, for a lot you cannot swap.

We draw the sample ourselves. We publish every test performed on the lot, including the ones nobody wants published. The record lives here, on our domain, where the seller cannot reach it.

Host your data → Verify a lot code Spot a fake COA

0
Results ever removed at a client's request. This is the number the business is built on.
100%
Of tests performed on a lot are published, pass or fail. Not a policy — the system enforces it.
8
Tests required before a peptide lot can be marked as passing. Most certificates carry two.
214 nm
The wavelength the peptide bond absorbs at, and where purity is actually measured.
01 Why certificates stopped meaning anything All six are in active circulation
FAILURE 01

The certificate is a web page

We have examined certificates whose purity value is passed in the URL. Change the number in the address bar and the page renders a new certificate. Nothing was measured a second time.

FAILURE 02

The seller picks the vial

When a manufacturer posts its own sample to a laboratory, the manufacturer chooses which unit gets tested. The result is true of that vial and says nothing about the lot you bought.

FAILURE 03

Only the good results are shown

Laboratories return results to the customer. The customer decides what reaches the public. A page of clean certificates can sit on top of any number of failures you will never see.

FAILURE 04

Purity is not content

A vial can be 99 % pure by HPLC and 65 % peptide by weight. The rest is water, salt and bulking agent. Net peptide content is the number that catches this, and it is the number most often left off.

FAILURE 05

No method, no meaning

A purity figure without a wavelength, a column and a gradient cannot be checked or reproduced. Most certificates in this market state none of them.

FAILURE 06

The document never expires

A result from two years ago is still being used to sell product made last month. Without a lot number binding it, one certificate can cover everything forever.

02 What an Attest214 record does differently Enforced by the system, not by policy
 Typical market COAAttest214 record
Who chose the sample The manufacturer, unstated Stated on every record — witnessed draw, random pull, retail purchase or client-submitted
Bound to a production lot Often "Batch: Unknown" A record cannot be published without a lot number
Incomplete result sets Rendered as a pass Rendered as INCOMPLETE, with the missing tests named
Selective publication Invisible Every record shows tests published of tests performed
Method disclosure Rarely stated Wavelength, column, gradient and retention time on every chromatographic result
Where the record lives A PDF or image on the seller's site Served from attest214.com, not editable by the seller
Ageing No expiry Issue date, age in days and retest date shown
03 The required panel A record missing any of these is not a pass

Peptides. Anything intended for injection additionally requires bacterial endotoxin and sterility.

Identity
LC-MS · observed against theoretical mass, tolerance stated
Confirms it is the right molecule
required
Purity
RP-HPLC-UV at 214 nm · column, gradient and retention time disclosed
Fraction of detected material that is the peptide
required
Net peptide content
Quantitative amino acid analysis, Kjeldahl nitrogen or qNMR
How much peptide is actually in the vial
required
Water content
Karl Fischer titration
Lyophilisation quality
required
Counterion content
Ion chromatography or ¹⁹F NMR
TFA load — cytotoxic above threshold
required
Residual solvents
Headspace GC-MS · ICH Q3C / USP <467>
Synthesis residues
required
Bacterial endotoxin
Kinetic chromogenic LAL · USP <85>
Fever response on injection
injectables
Sterility
Direct inoculation · USP <71>, 14 days
Live contamination
injectables
04 For suppliers Now accepting lots
STEP 01

We draw the sample

An officer pulls units at random from your sealed lot, or we buy your product at retail like any customer. You do not choose the vial. That is what makes the record worth something.

STEP 02

We run the full panel

Identity, purity, net peptide content, water, counterion, residual solvents, and endotoxin and sterility for injectables. Every method is disclosed on the record.

STEP 03

You get a code and a QR

Print it on the vial or carton. It resolves to a record on our domain that you cannot edit and we will not remove. Customers scan with the product in hand.

Start an enquiry →

Sample intake across the United States and Canada, with samples directed to the intake point for your region. European intake is planned — European suppliers can enquire now to join the waitlist.