| UNSPSC Code | 41116107 |
|---|---|
| NACRES | NA.24 |
| SMILES string | [Na+].[O-]C(=O)\C=C\C(=O)OCCCCCCCCCCCCCCCCCC |
| InChI | 1S/C22H40O4.Na/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-20-26-22(25)19-18-21(23)24;/h18-19H,2-17,20H2,1H3,(H,23,24);/q;+1/p-1/b19-18+; |
| InChI key | STFSJTPVIIDAQX-LTRPLHCISA-M |
| grade | certified reference material |
| agency | traceable to Ph. Eur. S0808000 |
| API family | sodium stearyl fumarate |
| CofA | current certificate can be downloaded |
| packaging | pkg of 1 g |
| technique(s) | HPLC: suitable |
| application(s) | pharmaceutical (small molecule) |
| format | neat |
| storage temp. | 2-30°C |
| Quality Level | 300 |
Answer:No. It is a 1 g pharmaceutical secondary-standard certified reference material used for analytical work rather than bulk formulation.
Answer:The CAS number is 4070-80-8, and its molecular formula is C22H39NaO4.
Answer:The certified material is traceable to relevant pharmacopoeial reference materials, including USP and European Pharmacopoeia standards.
Supelco Sodium Stearyl Fumarate Pharmaceutical Secondary Standard is a certified reference material for pharmaceutical analytical method development and quality-control testing. Sodium stearyl fumarate is a tablet lubricant with CAS 4070-80-8 and formula C22H39NaO4; its molecular weight is approximately 390.53 g/mol. The 1 g neat reference-material format is suitable for procedures requiring an identified analytical standard rather than bulk formulation material. The certified secondary standard is traceable to pharmacopoeial reference materials, including USP and European Pharmacopoeia sources, and supports suitable chromatographic and related analytical applications. In pharmaceutical testing, a reference material helps establish analyte identification and quantitative method performance. This certified grade should be distinguished from ordinary sodium stearyl fumarate manufacturing excipient. Use the lot-specific certificate for assigned reference information and associated uncertainty where relevant, and prepare analytical solutions by the validated laboratory procedure.
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