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Sulfanilamide 99% Min CAS 63-74-1 Medicine Grade / Industrial Grade Candidate sourcing visualHuman review
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Sulfanilamide 99% Min CAS 63-74-1 Medicine Grade / Industrial Grade Candidate

Sulfanilamide, also listed as sulphanilamide, 4-aminobenzenesulfonamide, or p-aminobenzenesulfonamide, is offered as a white powder with 99% min purity and CAS 63-74-1. This candidate should be qualified through CAS identity confirmation, grade alignment, impurity profile review, COA/TDS/MSDS availability, packing confirmation, and export documentation checks before RFQ or sample approval.

Quick buying facts

Identify the grade, package, and import market before comparing suppliers.

Use this page to check the product identity, common specification points, document scope, package notes, and destination-market questions before sending a China sourcing request.

CAS No.: 63-74-1Pharmaceutical intermediate / specialty chemical sourcing candidateHuman review
Identity and grade

Typical specifications

  • CAS No.: 63-74-1
  • Chemical name: Sulfanilamide / Sulphanilamide / 4-aminobenzenesulfonamide / p-Aminobenzenesulfonamide
  • Molecular formula: C6H8N2O2S
  • Molecular weight: 172.20
  • Appearance: White powder
  • Purity: 99% min as listed
  • Grade standard: Medicine Grade listed; source text also references Industrial Quality, requiring clarification
  • EINECS: 200-563-4
  • HS Code listed: 2935009090
  • Density listed: 1.08
Who uses this page

Target buyers

  • Pharmaceutical intermediate distributors
  • API and intermediate procurement teams
  • Chemical importers supplying regulated manufacturing customers
  • R&D and pilot-scale chemical buyers
  • Specialty chemical sourcing teams requiring COA-backed material
Before matching

Documents to check

  • CAS number, grade, assay, and impurity profile
  • SDS, COA, TDS, HS code, and transport classification
  • Destination-market import documents before supplier matching
Package and route

Packing notes

  • Listed packing: 50 kg/bag or customized by request
  • Confirm inner liner, moisture protection, palletization, and export carton or drum options
  • Request batch-specific net weight, gross weight, package dimensions, and shelf-life or retest date
  • Confirm whether sample packaging and commercial packaging use the same material-contact configuration
Applications and sourcing options

Check whether this product fits the buyer's actual application.

Clear application, grade, package, and document notes help separate real sourcing demand from a vague price check.

Use context

Common applications

  • Qualification as a sulfonamide-related intermediate where permitted by buyer specifications
  • Laboratory, R&D, or pilot procurement subject to internal approval
  • Commercial chemical distribution after destination-market compliance review
  • Pharmaceutical intermediate sourcing where documentation and impurity controls are validated by the buyer
How we compare

Sourcing options

  • Request sample with matching commercial specification and batch COA
  • Request medicine-grade and industrial-grade quotations separately
  • Use pre-shipment sample or third-party inspection for first commercial order
  • Compare suppliers on impurity limits, documentation depth, packing integrity, and export experience
  • Confirm CIF, FOB, DAP, or buyer-nominated forwarder options before final pricing
Human review

Compliance notes

  • Verify CAS, molecular identity, and synonym alignment against buyer internal specifications before procurement
  • Request batch COA, TDS, MSDS/SDS, commercial invoice, packing list, and certificate of origin as applicable
  • Clarify whether the supplier can support medicine-grade documentation, GMP-related statements, or only general chemical quality documentation
  • Confirm impurity profile, assay method, residual solvents if applicable, water content, heavy metals, and any pharmacopeial or internal standard references
  • Check destination-country import requirements, end-use restrictions, and buyer-side qualification obligations before shipment
  • Confirm dangerous goods classification, transport conditions, export control screening, and customs documentation before RFQ award
  • No regulatory approval, medicinal suitability, or unrestricted import status should be assumed from the listing alone
Buyer search paths

Related sourcing terms

These terms support long-tail discovery while keeping the page focused on useful product and China export buying context.

Sulfanilamide supplier ChinaSulphanilamide CAS 63-74-14-aminobenzenesulfonamide supplierp-aminobenzenesulfonamide 99%Sulfanilamide intermediateCAS 63-74-1 white powderSulfonamide intermediate sourcingMedicine grade sulfanilamide
RFQ questions before supplier matching

Turn this product into a quote request.

Share target market, quantity, packaging scope, artwork status, delivery destination, and required documents so CHN Chemicals can prepare a cleaner supplier comparison.

Questions to confirm
  • Can you provide a recent batch COA showing assay method, impurity profile, water content, and test standard?
  • Is the offered material medicine grade, industrial grade, or available in both grades? Please provide separate specifications if both are offered.
  • Which analytical methods are used for identity and purity confirmation, such as HPLC, GC, IR, or titration?
  • Can you provide SDS/MSDS, TDS, certificate of origin, packing list, commercial invoice, and any available GMP or ISO documentation?
  • What are the confirmed packing options for 1 kg sample, pilot quantity, and 50 kg commercial bags?
  • Is the quoted purity 99% min on dry basis or as-is basis?
  • What are the typical and maximum limits for related impurities, residual solvents, heavy metals, ash, and moisture?
  • What is the current batch availability, lead time, MOQ, sample policy, and pre-shipment sample process?
Checks before quote
  • Verify CAS, molecular identity, and synonym alignment against buyer internal specifications before procurement
  • Request batch COA, TDS, MSDS/SDS, commercial invoice, packing list, and certificate of origin as applicable
  • Clarify whether the supplier can support medicine-grade documentation, GMP-related statements, or only general chemical quality documentation
  • Confirm impurity profile, assay method, residual solvents if applicable, water content, heavy metals, and any pharmacopeial or internal standard references
  • Check destination-country import requirements, end-use restrictions, and buyer-side qualification obligations before shipment
  • Confirm dangerous goods classification, transport conditions, export control screening, and customs documentation before RFQ award
  • No regulatory approval, medicinal suitability, or unrestricted import status should be assumed from the listing alone
Next step

Send the product page with your target quantity and market. A sourcing manager can then confirm sample options, supplier fit, packaging details, and open document gaps.