ID
Identity testing
Analytical confirmation of identity using techniques appropriate to the molecule and matrix.
- LC-MS / molecular mass
- FTIR-ATR / spectral fingerprint
- Reference comparison
Independent analytical laboratory · Mexico
Specialized analytical testing. In Mexico.
Identity, purity, potency, impurities and Certificates of Analysis for peptides, pharmaceutical compounds and research substances — with results designed to be clear, traceable and useful.
Testing fromUS$99on select single-parameter tests
Based in MexicoLocal communication and simpler sample logistics
IndependentWe do not manufacture or sell the products we test
DocumentedTraceable results and controlled COA reporting
IdentityPurityPotencyImpuritiesResidual solventsWater contentCOA
Current testing access
Testing starts at US$99*
*Starting price applies to select single-parameter tests. Final scope and price are confirmed before sample shipment.
Due to current demand, new requests are being scheduled through our testing waitlist and reviewed in the order received.
Join the waitlistAnalytical capability in Mexico
Your sample should not have to leave Mexico to get serious analytical answers.
Altivex is being built to reduce dependence on laboratories outside the country and create a more direct path between client, sample, analysis and result.
Less logistics→Direct communication→Local analysis→Documented results
Mexico-based operationSpanish & English supportIndependent testingSpecialized service
Analytical services
Data that helps you make a defensible decision.
Altivex is designed for customers who need to understand what a sample contains, how much it contains and whether the analytical result is consistent with the declared specification.
%
Purity & potency
Separation and quantification to evaluate the principal component and the real quality of a sample.
- UHPLC / HPLC-PDA
- Assay / content
- Peak and impurity profile
RS
Residual solvents
Evaluation of relevant volatile solvents by gas chromatography with headspace sampling.
- Headspace GC-FID
- Selective quantification
- Specification-based reporting
H₂O
Water content
Moisture determination to support stability, formulation, storage and lot consistency decisions.
- Karl Fischer
- Quantitative results
- Sample traceability
M
Analytical methods
Method development, transfer, verification and optimization according to the intended analytical use.
- Method development
- Verification / transfer
- Technical documentation
COA
Certificate of Analysis
Consolidated analytical results in a clear COA linked to a specific sample or lot identifier.
- Results by parameter
- Method and specification
- Controlled documentation
Currently available testing
Defined panels for the samples customers are asking us to test now.
Choose a product below to join the testing queue. We confirm method fit, sample quantity, turnaround and final quotation before you ship a sample.
Testing starts atUS$99Select single-parameter tests. Final pricing varies by analyte, method and panel.
Available
GHK-Cu 50 mg
- Purity
- Identity
- Net Content / Mass
- Vial Photo
Available
SS-31 10 mg
- Purity
- Identity
- Net Content
- Vial Photo
Available
SS-31 50 mg
- Purity
- Identity
- Net Content
- Vial Photo
Available
Thymosin Beta-4 10 mg
- Purity
- Identity
- Net Content
- Vial Photo
Available
BPC-157 / TB-500 10 mg / 10 mg — Wolverine Blend
- Purity
- Identity of both components
- Net Content / Mass
- Vial Photo
Available
Retatrutide
- Purity
- Identity
- Mass / Content
Available
5-Amino-1MQ
- Purity
- Identity
- Mass / Content
Available
BPC-157
- Purity
- Identity
- Mass / Content
Available
GHK-Cu
- Purity
- Identity
- Mass / Content
Available
TB-500 / BPC-157 / GHK-Cu Blend
- Blend Purity
- Identity of each component
- Mass / Content
Available
Tirzepatide
- Purity
- Identity
- Mass / Content
Available
CJC-1295 / Ipamorelin Blend
- Blend Purity
- Identity of both components
- Mass / Content
Available
KPV
- Purity
- Identity
- Mass / Content
Available
NAD+
- Purity
- Identity
- Mass / Content
Core test typesAcross these 14 formulations, requirements consolidate into six analytical deliverables.
Availability reflects Altivex's current analytical intake plan and does not imply regulatory approval, product endorsement or suitability for human use.
Analytical platform
The right technique for the right analytical question.
No single test answers everything. Altivex combines complementary techniques to build stronger analytical evidence.
Tell us what you need to analyze →01
UHPLC / HPLC-PDAPurity, assay, impurity profile
Separation02
LC-MS / HRMSIdentity, molecular mass, confirmation
Identity03
FTIR-ATRSpectral fingerprint and identity verification
Spectrum04
Headspace GC-FIDResidual solvents and volatile compounds
Volatiles05
Karl FischerSpecific water determination
Moisture
CERTIFICATE OF ANALYSISCOA
IdentityConfirmed
Purity by HPLCReported result
WaterReported result
Residual solventsReported result
Certificates of Analysis
A useful analytical result ends in a useful document.
Altivex will provide Certificates of Analysis (COAs) that consolidate the analytical results obtained for each sample or lot, helping technical, quality and commercial teams review evidence consistently.
Unique identificationSample, lot and date linked to the report.
Documented methodTechnique and procedure reference used.
Clear resultsValues, units, specifications and observations.
Digital verification readyArchitecture designed to support validation of Altivex-issued reports.
An Altivex COA documents analytical results. By itself, it does not replace a sanitary registration, government authorization or regulatory product certification.
Quality & compliance pathway
Built from the beginning around laboratory discipline.
Altivex's quality roadmap is focused on technical competence, impartiality, traceability, document control and consistent operation.
Accreditation readiness
Quality system design aligned with principles applicable to testing and calibration laboratories.
Mexico regulatory pathway
Documentary and operational preparation for regulatory schemes that apply to Altivex's analytical scope.
Traceability & control
Chain of custody, sample identification, technical records and version control as part of the operating workflow.
Compliance status: references to ISO/IEC 17025 and COFEPRIS describe Altivex's intended quality and regulatory pathway. This website does not claim accreditation, authorization as a Tercero Autorizado, or government certification unless and until formally granted.
From sample to answer
A clear process, from request to reported result.
01
Define the need
Product, matrix, lot, parameters and objective of the analysis.
02
Analytical proposal
We confirm scope, method, sample quantity, cost and expected turnaround.
03
Receive & register
The sample receives an identifier and enters the traceability workflow.
04
Analyze & review
Defined tests are executed and the quality of the analytical data is reviewed.
05
COA & report
We deliver documented results for the evaluated sample or lot.
Ready to submit a sample?Start with the request form. We will confirm the required quantity and shipping instructions before you send anything.
Join testing waitlistWho we serve
Independent analysis for technical, quality and commercial decisions.
01Laboratories & manufacturers
02Distributors & suppliers
03Research & development teams
04Quality & procurement teams
05Universities & research centers
Request analytical testing
Tell us what you need to verify.
You do not need to know which instrument to request. Tell us what sample you have, what you need to demonstrate and how the result will be used. Altivex will define the appropriate analytical path.
01Technical & commercial response
02Scope & sample requirements
03Quotation before testing starts
MX
Service in Mexico
English and Spanish support for customers across Mexico.