For laboratory research use only. Every lot independently tested; certificates published by lot.

Thymosin Alpha 1 testing and quality control

Every lot of Thymosin Alpha 1 is tested by Freedom Diagnostics, an independent laboratory, for purity, identity and net content before release. Endotoxin and microbial results are added where those tests are run. Here is what each test measures, how results are reviewed, and how to check them yourself.

Last updated

≥95%
Release specification
LC-MS
Identity method, every lot
Independent
Third-party laboratory

The three methods

No single method answers every question about a peptide sample. Thymosin Alpha 1 is tested with complementary methods so that each one covers what the others can't.

HPLC-UV purity

Answers: how much of the sample is the main compound?

Reversed-phase high-performance liquid chromatography separates the sample's components by hydrophobicity, and a UV detector records each as a peak. Purity is the main peak's area as a percentage of all detected peak area.

Limits: does not identify the peak, and impurities that co-elute or absorb weakly in UV can be under-counted. More on HPLC

LC-MS identity

Answers: is the main compound Thymosin Alpha 1?

The separated sample enters a mass spectrometer via electrospray ionization, which gives the molecule one or more charges. The observed ions, near m/z 1555 (2+) and 1037 (3+), are matched against values calculated from Thymosin Alpha 1's molecular weight of 3108.32.

Limits: confirms molecular weight, not amino-acid order.

Net content

Answers: how much Thymosin Alpha 1 is in the vial?

The laboratory quantifies the main compound in the tested vial against a standard. It is reported in milligrams next to the labeled vial size.

Limits: measured on the vial tested; other vials from the same lot are expected to be similar but are not individually measured.

Quality-control process

The path every lot follows from production to a published certificate.

  1. Lot assignedA lot number is assigned and printed on every vial label.
  2. Sample sentVials from the lot go to Freedom Diagnostics, an independent lab.
  3. AnalysisHPLC-UV purity, LC-MS identity and net content, plus endotoxin and PCR where listed.
  4. ReviewResults are compared with the stated specification: ≥95% purity, identity confirmed.
  5. PublishedThe lot record is posted at /coa/ under its lot number.
  6. VerifiableAnyone can look the lot up at /verify/ and confirm it with the laboratory.

Release specification

Thymosin Alpha Labs’ stated release specification is ≥95% HPLC-UV purity with identity confirmed by LC-MS. Current lots test at , .

Batch identification

Each lot carries a unique lot number (for example LOT123) printed on every vial label and on the certificate. The laboratory also assigns its own reference numbers (accession number and search code), which are listed on each lot page for cross-checking.

Document retention

Certificates remain published in the archive after a lot sells through, so the documentation for any vial stays available.

About the laboratory

Freedom Diagnostics is an independent, U.S.-based analytical testing laboratory. Its certificates for Thymosin Alpha 1 are signed by the laboratory's principal chemist and carry a QR code linking to the laboratory's own record.

Laboratory contact: freedomdiagnosticstesting.com, Admin@FreedomDiagnostics.net.

Verify a result

  1. Find the lot number on your vial. It is printed on the label, for example LOT123.
  2. Look it up. Enter it at thymosinalpha.bio/verify, or open the matching lot in the COA archive.
  3. Check the lab's own record. Scan the Freedom Diagnostics QR code printed on the certificate, then search for klow.bio under the Company tab to view the laboratory record.
  4. Compare the details. Lot number, the laboratory’s reference numbers, purity and dates should match exactly.

Results across current lots

Certificate in progress. The current batch is with the testing laboratory. Its certificate of analysis will be published here, with purity, identity and net content, as soon as the report is issued. Current availability on Klow.bio.

Identity

IonCalculationExpected m/zObserved on COAs

Expected values are calculated by Thymosin Alpha Labs from the average molecular weight (3108.32 g/mol; H+ 1.0073, Na+ 22.99, K+ 39.10). Observed values are as printed on each lot's mass confirmation panel.

Purity

What a certificate of analysis does and doesn't show

  • A COA reports the identity, purity and content of the specific sample tested, on its test date. Results apply to that lot only.
  • HPLC purity measures the main peak relative to other detected components. It does not identify the peak on its own; the separate identity test (LC-MS) does that.
  • Mass confirmation matches molecular weight. It does not by itself confirm amino-acid order.
  • Endotoxin and microbial results apply only where those tests appear on the certificate. Lots without them are marked "Not tested".
  • A certificate does not establish stability after the test date or suitability for any particular purpose.

Method guides

Testing questions

How is Thymosin Alpha 1 analyzed?

Thymosin Alpha 1 is analyzed with complementary methods: HPLC-UV for purity, LC-MS for identity, a quantitative measurement for net content, and, where listed, LAL endotoxin and PCR microbial testing. Results are published per lot at thymosinalpha.bio/coa/.

Who tests Thymosin Alpha 1?

Every lot is tested by Freedom Diagnostics, an independent third-party analytical laboratory. Thymosin Alpha Labs does not test its own material for published certificates.

What purity does Thymosin Alpha 1 test at?

Purity is reported per lot by HPLC-UV.

How is the identity of Thymosin Alpha 1 confirmed?

By liquid chromatography–mass spectrometry (LC-MS), performed by Freedom Diagnostics on every lot. LC-MS separates the sample and measures the mass of the main component, confirming it has the molecular weight expected for the compound.

Is Thymosin Alpha 1 tested for endotoxin?

Endotoxin and microbial testing are reported per lot. Every lot page in the COA archive states whether those tests were performed.

What is HPLC testing, and what does the purity percentage mean?

HPLC (high-performance liquid chromatography) separates a sample's components so each appears as a peak. The purity percentage is the main peak's share of all UV-detected peak area. It does not confirm identity (the separate LC-MS test does) or measure the amount of peptide in the vial (net content does).

What is a Thymosin Alpha 1 COA?

A Thymosin Alpha 1 certificate of analysis is the testing laboratory's report for one lot: the lot number, test dates, methods and results for purity, identity and net content. Thymosin Alpha Labs publishes every lot's COA as a readable page at thymosinalpha.bio/coa/.

Where can I find the COA for my vial?

Find the lot number printed on your vial label and enter it at thymosinalpha.bio/verify/, or open that lot in the COA archive at thymosinalpha.bio/coa/.

How do I confirm a COA with the laboratory?

Scan the Freedom Diagnostics QR code printed on the certificate, then search for klow.bio under the Company tab to view the laboratory record.

Why is the measured net content different from the vial size?

Net content is the laboratory's measurement of peptide in the tested vial.

Buy Thymosin Alpha 1

5 mg vials. The current batch's certificate is in progress. Current purchasing is available through Klow.bio.