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GL Biochem (Shanghai) (revision 37)

Old revision·19:29, 4 Jan 2025·UnderfillUna

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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.
GL Biochem (Shanghai) 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 nameGL Biochem (Shanghai) Ltd.
Trading nameGL Biochem
Other designationsGLS
Identity
FoundedReported 1998 (self-published)
HeadquartersShanghai, China
IndustryResearch-compound supply
Shop domainVisit GL Biochem
Products and documentation
Product scopecustom peptides and amino acids
Catalogue sizeNot documented
DocumentationBatch certificate of analysis reported with orders
Independent reportsSubmitted to this wiki by purchasers; see §Independent testing record
Organisation infobox · conventions

GL Biochem (Shanghai) Ltd. (trading as GL Biochem; glbiochem.net) is a peptide-synthesis company based in Shanghai, China, described in available sources as founded in 1998 and operating at a scale substantially larger than the research-compound suppliers otherwise covered on this wiki, supplying custom peptides and amino acid derivatives internationally.[1][2]

The organisation is one of twenty 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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Available sources describe the organisation as founded in 1998, which would make it the oldest entity covered on this wiki and place its establishment two decades before the current research-compound retail market.[2] It is described as holding ISO 9001 certification and operating under a cGMP quality system, with a workforce in the low thousands and a substantial patent portfolio.[2]

Those figures come from the organisation's own material and are reproduced here as attributed claims rather than as verified facts, in accordance with Project:Verifiability. They are unusually specific for this sector, and a certification claim in particular is not a fact until assessed against the applicable framework.[5]

The organisation occupies a different position in the supply chain from most entities covered here. A synthesis house selling custom peptides and amino acid building blocks to laboratories and to other companies is a supplier to the sector rather than a retailer within it, and much of the material eventually sold as a research compound originates upstream of the entity that sells it.[2]

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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The organisation's described activity is custom synthesis to specification and supply of protected amino acid derivatives and coupling reagents — the inputs to solid-phase synthesis rather than its retail output.[2]

Purchaser reports reaching this wiki are consequently different in character from those for retail suppliers: they describe quotations, specification agreement, lead times measured in weeks, and certificates reporting purity, mass confirmation and amino acid analysis.[6] Reported documentation has been consistently more complete than for retail suppliers, which is what a laboratory-supply market expects rather than a distinguishing achievement.[7]

Product range

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ClassRepresentative activityDocumentation reported
Custom peptide synthesisSequence to specification, milligram to kilogramPurity, mass confirmation, amino acid analysis
Protected amino acidsFmoc- and Boc-protected derivativesSpecification and lot certificate
Coupling reagents and resinsSynthesis consumablesSpecification sheet
Catalogue peptidesReference and research sequencesLot certificate

The presence of amino acid derivatives, resins and coupling reagents in the catalogue is what most clearly places the organisation upstream: those are what a synthesis laboratory buys, not what a research-compound purchaser buys.[2]

Independent testing record

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Reports submitted to this wiki on GL Biochem material are fewer in number than for the large retail suppliers but more complete in content, typically including mass confirmation and, in several cases, amino acid analysis alongside a purity figure.[6]

Amino acid analysis is the technique that establishes peptide content as a mass fraction rather than inferring it, and its presence on a certificate answers the question that a purity figure alone leaves open.[7] Its appearance on certificates from an upstream supplier and its near-absence from retail certificates is the clearest illustration on this wiki of the documentary difference between the two markets.

See also

References

  1. ^ 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 e f 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. ^ Research-use-only labelling practice; see Research use only for the legal and commercial function of the phrase.
  4. ^ 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. ^ 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.
  6. ^ a b 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.
  7. ^ a b United States Pharmacopeia, General Chapter <1503>, "Quality Attributes of Synthetic Peptide Drug Substances" (informational). USP–NF, current revision.