Shandong Aishi Biotechnology

Is Shandong Aishi Biotechnology legit?

TitrateLab has 89 lab test records for Shandong Aishi Biotechnology, tested from to , covering 7 product names. Median measured purity is 99.9% across 87 purity tests; 1 was below 90%. 2 tests did not detect the expected compound. None of the 11 classified endotoxin tests failed. 2 results reported a zero amount. Lab results describe the batches that were tested, not every product or order.

89Test records7 recorded name groups

Reports by test date

2025-10-062026-10-05

Select a month to list its reports below.

99.9%Median purity87 positive purity tests
0Community reviewsNo approved reviews yet
0

Endotoxin failures

11 classified tests · All time

2

Expected compound not detected

89 reported purity outcomes · All time

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Underfilled >15%

No fill test in the last 6 months

Not tested
—

Overfilled >15%

No fill test in the last 6 months

Not tested
2

Reported zero amount

89 numeric amount results · All time

Lab reports

89 test records on file · October 2025 to October 2026

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Test results

How the fills compare

0 fill tests · All time

Measured against the printed amount. Finnrick quantities are excluded.

Beyond the purity average

87 positive tests

Mean 99.4% · Median 99.9%. The 90% grouping is not a safety threshold.

Test coverage & missing results

0 records have no usable purity outcome. 89 do not have a comparable fill test. 78 lack a classified endotoxin result. A classified pass does not mean no endotoxin was detected.

Reports behind these results

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Shandong Aishi Biotechnology reviews

Buyer experiences—not lab results or verified purchases.

0Positive
0Neutral
0Negative
0Unclassified

No approved reviews on file yet.

Recorded offers—not a live stock guarantee. Package quantity, delivery market and price basis stay attached.

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Research involving Shandong Aishi Biotechnology

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Published investigations, with the sources and context behind the findings.

Questions about Shandong Aishi Biotechnology

Answers based on the published evidence—not a vendor endorsement.

Is Shandong Aishi Biotechnology legit?

TitrateLab has 89 lab test records for Shandong Aishi Biotechnology, tested from October 6, 2025 to October 5, 2026, covering 7 product names. Median measured purity is 99.9% across 87 purity tests; 1 was below 90%. 2 tests did not detect the expected compound. None of the 11 classified endotoxin tests failed. 2 results reported a zero amount. Lab results describe the batches that were tested, not every product or order.

How to check if a peptide vendor is legit: six checks, and what they cannot prove.

What is Shandong Aishi Biotechnology's average purity?

99.4% mean measured purity across 87 positive purity tests; 1 below 90%. The 90% grouping is not a safety threshold. 2 additional tests did not detect the expected compound.

How many Shandong Aishi Biotechnology lab test records has TitrateLab tracked?

TitrateLab has 89 lab test records for Shandong Aishi Biotechnology. Tested from 2025-10-06 to 2026-10-05. A test record is not necessarily a unique certificate.

How do Shandong Aishi Biotechnology's measured fills compare with the label?

Last 6 months: no comparable fill test. All time: no comparable fill test. The measured amount is compared with the printed label. Finnrick quantity comparisons are excluded because they use a vendor batch claim. Missing tests are not passes.

Has Shandong Aishi Biotechnology failed an endotoxin test?

Of 11 classified endotoxin tests, 0 failed, 0 were borderline and 11 passed. A pass does not mean no endotoxin was detected.

Sources, definitions & limits

Names on reports; vendor role unverified. A test record is not necessarily a unique certificate.

The reports describe the batches that were tested, not an untested vial or an offer from this vendor.

89 published records are attributed to this vendor. The current certificate index excludes 0 repeated records using file hashes and supported lab verification links. Missing identity keys can leave repeated certificates. Recorded name groups can include variants, mixtures and unclassified names.

Evidence dates describe the tested samples, not when the vendor was founded, current stock, or a performance trend. Purity uses positive measurements only. Exact-zero purity is a not-detected identity outcome, not proof of an empty vial. A zero measured amount requires an explicit numeric amount result; missing amounts are not zero.

Underfills and overfills here exceed 15% in either direction against the printed amount. Vendor batch claims are not used; Finnrick quantity comparisons are excluded. Recent outcomes cover 2026-05-02 through 2026-11-02, inclusive. The summary, charts and FAQ use these same definitions. Missing tests are not passing results.

Endotoxin failures, borderline outcomes and passes use the recorded lab verdict. A pass is not proof of no endotoxin. Only 11 records have a classifiable result. Community sentiment describes reviews, not laboratory measurements or independently verified purchases. Results are not certification, medical advice or endorsement.

Independent evidence · Not certification or endorsement · Browse vendors

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