SERVICES & CAPABILITIES

Analytical Capabilities

HPLC, MS and identity testing for development and release.

20+Years of experience
GMPQuality mindset
mg → kgFlexible scale
GlobalCustomer support

Overview

Analytical science is central to peptide quality. We develop and apply methods for identity, purity, related substances and characterization throughout the project lifecycle.

Good analytics shorten decision cycles: you know what you made, how pure it is, and which impurities matter before the next scale-up step.

Core capabilities

  • HPLC/UPLC purity and impurity profiling
  • Mass spectrometry for identity confirmation
  • Method development with eventual QC use in mind
  • Data packages suitable for research or regulated contexts

Tell us your current methods and release needs — we will align analytical work to your project phase.

Chromatography

HPLC/UPLC methods for purity and impurity profiling.

Mass spectrometry

Identity confirmation and structural insight.

Release mindset

Methods designed with eventual QC use in mind.

How we work

A clear path from inquiry to delivery — designed for research and regulated programs alike.

01

Share your requirements

Sequence or target, purity, quantity, timeline and documentation needs.

02

Technical assessment

Our specialists review feasibility, route options and analytical approach.

03

Proposal & kickoff

Clear quotation, milestones and a dedicated project contact.

04

Manufacture & deliver

Synthesis, purification, testing and shipment with supporting documents.

What you can expect

Transparent deliverables and documentation matched to your project phase.

  • Defined specifications and acceptance criteria
  • Certificate of Analysis (COA) where applicable
  • Analytical chromatograms / MS data on request
  • Batch documentation aligned to project phase
  • Secure packaging and cold-chain options
  • Responsive scientific & commercial support

Why partners choose Scentsummer

Science first

Route selection, impurity control and analytics are treated as core project work — not afterthoughts.

Flexible scale

From research milligrams to larger campaign quantities, with continuity as programs mature.

Reliable communication

Milestones, risks and documentation needs stay visible through a dedicated project contact.

Frequently asked questions

How fast can you quote?
Most catalog and standard custom requests receive a response within one business day. Complex CDMO programs may need a short technical review first.
What purity grades are available?
We support a range of research and higher-purity grades. Tell us your application and we will recommend a suitable specification.
Do you support GMP supply?
Yes. For clinical and commercial peptide API programs we operate with a GMP quality mindset and phase-appropriate documentation.

View all FAQs →

NEXT STEP

Get a quote that moves your project forward

Sequence + purity + quantity + timeline — send it now via quote form, contact, or WhatsApp.