Quality & testing

Purity you can verify, not just claim.

Every lot is characterized before release and documented lot-by-lot. Here’s exactly how material is tested, what’s on a Certificate of Analysis, and the standards behind sourcing.

The process

Four checks before a lot ships.

01

Identity

Compound identity is confirmed by electrospray mass spectrometry (ESI-MS) against the expected molecular weight.

02

Purity

Reversed-phase HPLC with UV detection quantifies purity as area %, resolving related impurities from the main peak.

03

Appearance & fill

Each lot is checked for appearance, fill and reconstitution behavior against the release specification.

04

Documentation

Results are compiled into a lot-specific Certificate of Analysis that ships with every order.

Quality at a glance

The data behind the documentation.

Release testing produces numbers, not adjectives. A snapshot of recent performance across lots.

HPLC purity · recent release lots

Area % · dashed line = 99% release threshold
989999100100SMG99.2%TZP99.4%RET99.1%BPC99.0%TB599.3%CJC98.9%
Measured purityRelease threshold

Lots passing release

99.6%release pass rate
Trailing 12 months
across all compounds

Certificate of Analysis

Lot SMG-2406-B · Semaglutide
0.02.55.07.510.0mAUmin99.2% area · RT 6.82 min
MethodRP-HPLC / UV 214 nm
Purity (area %)99.2%
IdentityESI-MS confirmed
Retention time6.82 min
AppearanceWhite solid
ReleasePass
Reading a COA

What’s on every certificate.

A Certificate of Analysis is the analytical record for a specific lot. It ties the vial in your hand to the data behind it.

  • Compound & lot — the exact material and batch.
  • Purity & method — area % with the HPLC method and detection wavelength.
  • Identity — mass-spec confirmation against expected MW.
  • Retention time & appearance — chromatographic and visual checks.
See COAs on product pages
Independent verification

Third-party testing on representative lots.

Beyond in-house release testing, representative lots are sent to independent analytical laboratories to corroborate identity and purity. These reports are available on request before you order.

  • Independent HPLC purity confirmation
  • Orthogonal identity confirmation by MS
  • Reports retained and traceable to lot
Request a verification report

HPLC

Purity by area %

Mass spec

Identity confirmation

COA

Per lot, every order

Traceable

Manufacture to dispatch

Sourcing standards

Controlled from synthesis to shipment.

Quality starts upstream of the analytics. Material is produced and handled under documented controls at every step.

Controlled synthesis

Material is produced to defined specifications with batch records that follow each lot through to release.

Intake screening

Incoming lots are checked against specification before they are accepted into inventory and listed for sale.

Cold-chain handling

Lyophilized material is stored and shipped under temperature control to preserve integrity in transit.

RUOAll products are research chemicals supplied for laboratory research use only — not for human or veterinary consumption, diagnostic or therapeutic use.