Fluopyram 98% TC Fungicide

This catalogue entry lists Fluopyram at 98% as TC, with CAS number 658066-35-4. Its procurement audience is formulators, manufacturing partners and registration holders evaluating technical material as an input to a formulated product. The 98% declaration describes the listed active content; the current offer must state the assay basis, acceptance limits and relevant impurity profile.

FAO defines technical material (TC) as material containing an active ingredient and associated impurities that is formulated before pesticide use. The procurement stage therefore differs from a finished crop-protection formulation. This entry does not provide a direct field dilution, crop list or application-rate instruction.

Compare TC with the separate Fluopyram + Tebuconazole SC

The catalogue also lists Fluopyram + Tebuconazole 17.5% / 17.5% SC. That entry contains two listed actives in a suspension concentrate, while this entry identifies Fluopyram technical material. A 98% TC and a 17.5% / 17.5% SC cannot be selected or accepted using the same purchase specification.

For TC, the review concerns the active ingredient, impurities, manufacturing source and suitability for the intended formulation or regulatory file. For the separate SC, the buyer must review both actives, the physical formulation and the finished-product registration and label. A higher catalogue percentage does not establish better field performance or regulatory equivalence.

Read the full stage and document comparison in Fluopyram 98% TC vs SC: a buyer guide.

Build the technical-material acceptance specification

Ask for the current Fluopyram technical specification and a clear statement of which test methods and limits apply. Agree the active-content assay and tolerance. Request the relevant impurity information and applicable limits for the manufacturing source and destination requirements. The public page does not publish a measured impurity profile, a batch assay or a source-equivalence determination.

• Identity: active-ingredient name, CAS 658066-35-4, TC designation and the assay basis.
• Quality: agreed active-content limit, analytical method, relevant impurity limits and any required physical or storage parameters.
• Traceability: manufacturing-source identification, sample lot, testing date and the proposed commercial-lot document scope.

The general scope of FAO pesticide specifications includes active content, relevant impurities and material properties. A public FAO reference explains those concepts; it does not prove that this offered source has a FAO evaluation or that a particular batch conforms.

Separate the SDS, specification and batch evidence

Request an SDS matching the exact technical material and handling requirements. Keep the supplier specification with its agreed acceptance limits. Ask whether an identified sample COA or a batch COA is proposed, and which methods, dates and results it will contain. Link the evaluated sample to its source lot and state how the commercial batch will be accepted. A COA marked TEST in the site library is a document example, not an identified shipment certificate.

Define the registration and source-document scope

Give the destination country, the intended product stage and whether the request supports technical-material registration, source approval, an equivalence review or a formulated-product dossier. Ask which manufacturing and analytical information can be supplied for that specific route and whether access requires an agreed confidentiality arrangement. Data availability, source acceptance and local authorization need written confirmation for the actual offer.

Crop, disease, rate and timing claims must be assessed for the resulting registered formulation. They are not established by a TC assay or by copying the claim set of a different Fluopyram product. The upstream material review and the finished-label review should each be completed against their own required evidence.

Send a formulator’s quotation brief

Specify Fluopyram 98% TC, required quantity, destination, intended formulation or registration route and the acceptance standard. Add the sample amount and purpose, impurity-information scope, analytical documents, packaging and handling requirements, label language, Incoterm and delivery window. Request written confirmation of the available material, document scope and pack format. Approve the technical specification and sample or lot acceptance requirements before the commercial order is released.