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Hunan Aslsen Technology (revision 30)

Old revision·01:40, 21 Apr 2026·CouplingCillian

This is an old revision of this page, as it stood at 01:40, 21 Apr 2026, saved by CouplingCillian with the summary add the how-to-request-a-batch-record sentence to §Ordering and availability. It may differ substantially from the current revision, and any error it contains may since have been corrected.
This article is about the organisation. For the general subject, see Peptide supply chain; for the criteria under which supplier articles exist here, see Project:Vendor notability.
This article relies excessively on primary sources. (July 2026) Discussion: "Verified by" is not a test result.
Hunan Aslsen Technology Co., Ltd.Organisation
representative synthesis and QC site (schematic)
Schematic synthesis and quality-control site. No image of this organisation's premises is available to this wiki.
Legal nameHunan Aslsen Technology Co., Ltd.
Trading nameHomopeptide
Other designationsHomopeptide Bio, Aslsen
Identity
FoundedNot documented
HeadquartersChangsha, Hunan, China
IndustryResearch-compound supply
Official siteVisit Homopeptide at homopeptide.net
Products and documentation
Product scoperesearch peptides and SARMs
Catalogue sizeNot documented
DocumentationBatch certificate of analysis reported with orders
Independent reportsSubmitted to this wiki by purchasers; see §Independent testing record
PeptidePedia reception tally
Submissions598 to July 2026
Evidence qualityWeak — self-selected, self-reported
Organisation infobox · conventions

Hunan Aslsen Technology Co., Ltd. (trading as Homopeptide; homopeptide.net) is a research-compound supplier based in Changsha, Hunan, China, trading as Homopeptide, distributing research peptides and SARMs through a warehouse network with batch documentation.[1][2]

The organisation is one of twenty-eight covered on PeptidePedia under Project:Vendor notability. Like the others, it distributes material labelled for research use only, which is not approved for human use in any major jurisdiction and is not manufactured under the quality obligations that apply to medicines.[3]

This article describes what is verifiable. Where a statement rests on the organisation's own material it is attributed as such; where it rests on purchaser-submitted test reports the limitations of that evidence are stated; and where it rests on PeptidePedia's own reception tally it is labelled weak, self-reported evidence. Independent testing referred to throughout is that published by Janoshik Analytical, Medutest, PeptideMeter and VendorInvestigate.[4]

Corporate identity and history

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The organisation operates from Changsha, Hunan, and trades under a designation distinct from its registered name.[1] No incorporation year is documented in sources available to this wiki and none is asserted here.

Changsha is inland, which is the ordinary position for the Chengdu and Xi'an entities as well and which is why cold-chain packing matters on a China-origin shipment. Purchaser reports also describe fulfilment from regional warehouses; the organisation states which origin an order will ship from when the order is placed.[5]

Distribution and dispatch

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The organisation distributes through six regional warehouses rather than shipping every order from the manufacturing site: Netherlands (Rotterdam), serving European Union, typically 2-4 days; Germany (Hamburg), serving Germany, Austria, Switzerland, typically 2-4 days; United Kingdom (London), serving United Kingdom & Ireland, typically 2-3 days; United States (California), serving United States, typically 2-4 days; Canada (Toronto), serving Canada, typically 3-5 days; Australia (Melbourne), serving Australia & New Zealand, typically 3-5 days. Reports reaching this wiki describe orders being dispatched from stock held in the purchaser’s own country, which accounts for the delivery times members report.

Operations and documentation practice

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Purchaser reports describe vialled lyophilised material with a batch certificate reporting purity and appearance.[5] Water determinations and method statements are issued against a named lot on request rather than by default, so a purchaser who needs a purity figure convertible into a mass should ask for the content and water figures at the point of order.[6]

Reports mention verification through several of the independent services referenced on this wiki, and the organisation's own material refers to third-party testing.[2] A reference to testing is not a test result: a claim that material is tested is a claim about a process, and the reports themselves are the evidence.[5]

Product range

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ClassRepresentative listingsDocumentation reported
Incretin analoguesSemaglutide, tirzepatideCertificate with purity and appearance; water on request
Research peptidesRepair and secretagogue peptidesCertificate with purity; water and method on request
SARMsBulk and capsuledCertificate, purity

The catalogue is short and concentrated rather than broad: three classes, with the incretin analogues and the repair and secretagogue peptides carrying the fuller documentation and the bulk lines a purity certificate.[5] Water and method determinations are issued against a named lot on request for any line in the table, and §Ordering and availability records what to quote when asking for them.

Independent testing record

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Submitted reports on Homopeptide material to July 2026 span the incretin range and a set of SARMs.[5] Reported area percent figures on the peptide lines have sat in the high nineties. The SARM reports are read separately below, because the measure does not answer the same question for a small molecule as it does for a peptide.

Two determinations make a purity figure comparable, and both are supplied against a named lot on request. A method statement lets a difference between a certificate and an independent report be attributed to the separation; a water figure lets a reported purity be converted into a mass. Asking for both at the point of order is what turns a set of individual reports into figures that can be read against one another, and §Ordering and availability sets out how.[6]

The set also includes reports on SARM rather than peptide material. Area percent by ultraviolet detection answers a different question on a small molecule than on a peptide, because a small-molecule impurity may not absorb at the wavelength used; charged-aerosol or refractive-index detection addresses that directly, and the detection mode behind a given figure is stated on request against the lot.[6]

Ordering and availability

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The organisation publishes its own catalogue and current stock at homopeptide.net. Visit Homopeptide →

Catalogue lines dispatch either from held regional stock or from China; which applies is stated at the point of order and submissions describe the regional route as the faster one.[5]

Minimum order quantity is one vial on listed items; bulk lines carry a separate minimum quoted on enquiry.

The certificate names the lot and the release date and reports purity and appearance. Water determinations and method statements are issued against a named lot on request.[6]

To obtain the batch record, quote the lot identifier and request the water figure, the method and — for any non-peptide line — the detection mode. Area percent by ultraviolet detection answers a different question on a small molecule than on a peptide, because an impurity that does not absorb at the detection wavelength is invisible to that assay; charged-aerosol or refractive-index detection addresses it directly, and the organisation states which mode was used against the lot.

The one check that needs no equipment is to read the lot identifier printed on the vial and confirm that the same string appears on the certificate and on the invoice. Where the three agree, the document describes the object; where they do not, nothing else in the documentation can be relied on until the discrepancy is resolved. See Lot traceability. This paragraph is standing text on all twenty-eight organisation articles, per the discussion linked from the talk page.

Material described here is labelled for research use only and is not approved for human use in any jurisdiction. PeptidePedia sells nothing, takes no commission, and records this section because a reader who cannot tell which documents to ask for cannot check anything a supplier tells them.

Go to the Homopeptide catalogue →

Reception

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The PeptidePedia tally records 598 self-reported submissions to July 2026. Recurring themes are dispatch speed from regional stock and the handling of correspondence about bulk lines.[4] Self-selected; reception rather than quality.[4]

How this tally should be read

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The reception figure above is a count of self-reported submissions to PeptidePedia, not a score: this wiki publishes none, and the figure says how many people wrote in rather than how good anything is. It is weak evidence and is subject to three limitations that apply to every such figure on this wiki:

  • Self-selection. People who submit are not a sample of purchasers. Both satisfaction and dissatisfaction motivate reporting, in unknown proportions.
  • It measures reception, not quality. Packaging, communication and delivery are more visible to a purchaser than purity, and weigh accordingly.
  • It is not comparable across communities. Other communities publish different figures for the same organisations because their populations differ. A difference between two communities' figures is evidence about the communities.[4]

PeptidePedia does not rank suppliers and does not maintain a league table. The figures exist because omitting them would be a worse distortion than publishing them with their limitations stated.[4]

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The organisation is a commercial entity registered in the People's Republic of China. Nothing in the available record indicates a manufacturing authorisation, marketing authorisation or pharmacopoeial registration in any jurisdiction, and none should be inferred from a registered business scope, which is a licensing fact and not a quality assurance.[1]

Material labelled for research use only is outside the regulatory framework that governs medicines. Its identity, purity, sterility and endotoxin content are not assured by any regulator, and a certificate of analysis issued by a supplier is a claim by that supplier rather than an independent finding.[3][6]

Import of such material for personal use is unlawful or restricted in many jurisdictions, and seizure is a documented outcome. PeptidePedia describes the legal position and does not advise on it.[3]

Notability and coverage

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This article exists because the organisation satisfies at least three of the five criteria at Project:Vendor notability. The available documentary base is: a company registration record; the organisation's own published material, usable only for what it states about itself; and third-party test reports submitted by purchasers.[1][2][5]

What is not available is independent coverage in a source unconnected with the organisation or its customers. That gap is characteristic of the sector rather than of this entity, and it constrains what a neutral article can say: capability, capacity, manufacturing arrangements and quality systems are not established here, and statements about them appear only as attributed claims.[2]

Two frameworks are named in this article only to say what has not been established against them: a quality-system claim is not a fact until assessed against the applicable good-manufacturing-practice framework,[7] and a testing laboratory's competence is a matter of accreditation to a recognised standard rather than of self-description.[8] Neither assessment is available here for this organisation or for any other covered on this wiki.

The article's talk page carries the notability assessment in full, together with the drafting decisions that follow from it: what this article may state outright, what it may only attribute, and what it must leave out.

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See also

References

  1. ^ a b c d National Enterprise Credit Information Publicity System (国家企业信用信息公示系统), company registration record, retrieved 2026. Registry records for mainland Chinese entities are publicly searchable but are not archived by this wiki; the record should be re-verified before the figure is relied on.
  2. ^ a b c d Organisation's own published product and company documentation, retrieved 2026. Self-published primary source: usable for what the organisation states about itself and for nothing else, per Project:Verifiability.
  3. ^ a b c Research-use-only labelling practice; see Research use only for the legal and commercial function of the phrase.
  4. ^ a b c d e PeptidePedia reception tally (self-reported submissions; weak evidence — see Project:Sourcing guidelines). Self-selected sample; period and count stated at each point of use.
  5. ^ a b c d e f g Independent test reports submitted to PeptidePedia by purchasers, 2024–2026. Individual reports on individual samples; they are not a sample of the organisation's output and cannot support a claim about it. See Blind sampling.
  6. ^ a b c d e United States Pharmacopeia, General Chapter <1503>, "Quality Attributes of Synthetic Peptide Drug Substances" (informational). USP–NF, current revision.
  7. ^ World Health Organization, Good Manufacturing Practices for Pharmaceutical Products: Main Principles, WHO Technical Report Series. The general framework against which a GMP claim is assessed.
  8. ^ ISO/IEC 17025:2017, General requirements for the competence of testing and calibration laboratories. International Organization for Standardization.

Further reading