Sodium Valproate EP Impurity F CAS 2430-27-5
| CAS No. | 2430-27-5 |
| Molecular Formula | C8H17NO |
| Molecular Weight | 143.23 g/mol |
| Category | Pharmacopoeial Impurity Standards / EP Impurities |
| Availability | In Stock |
Chemical Structure
Description
Compared with other compounds in its class, the molecular weight of 143.23 g/mol gives Sodium Valproate EP Impurity F distinctive chromatographic separation conditions and mass-spectrometry parameter settings.
CATO supplies Sodium Valproate EP Impurity F (CAS 2430-27-5), a pharmacopoeial impurity reference standard (molecular formula C8H17NO, MW 143.23 g/mol) used for the identification and quantification of trace impurities in APIs.
Owing to an amide group, a hydroxyl group, an ether linkage, Sodium Valproate EP Impurity F is typically white to off-white liquid. Its solid-state physicochemical attributes — including a molecular weight of 143.23 g/mol — guide the selection of appropriate sample preparation and analytical techniques. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.
Recommended for quantitative analysis by HPLC, GC, LC-MS/MS, or GC-MS as an external calibration standard; it can also be used for spiked-recovery experiments, LOD/LOQ determination, and LC-MS/MS multiple-reaction-monitoring (MRM) calibration.
As a certified reference material (CRM), Sodium Valproate EP Impurity F meets the metrological traceability requirements of ISO/IEC 17025 laboratories. Batch-to-batch consistency is monitored via control charts to guarantee comparable assigned values across lots.
Physical & Chemical Properties
| Molecular Formula | C8H17NO |
| Molecular Weight | 143.23 g/mol |
| Purity | >95% |
| Storage | Store at 2-8°C, protect from light |
| Solubility (reference) | Soluble in methanol, acetonitrile, DMSO, water (slightly soluble) |
| Stability | Light-sensitive; avoid direct strong light |
| Degree of Unsaturation (DBE) | 1.0 |
| CAS Registry Year (est.) | 1957 |
| Nitrogen Atoms | 1 |
Related Sodium Standards
- Sodium Valproate EP Impurity K (CAS 5343-52-2)
- Sodium Valproate EP Impurity C (CAS 62391-99-5)
- Sodium Valproate Impurity 35 (CAS 6137-09-3)
- Valproate Impurity 49 (CAS 40239-27-8)
- Sodium Valproate Impurity 27 (CAS 1575-72-0)
- Sodium Valproate Impurity 18 (CAS 542-05-2)
- Sodium Valproate Impurity 19 (CAS 616-62-6)
- Valproate Impurity 66 (CAS CATO-C4X-116666)
Recommended Standards
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- Pitolisant impurity 17 (CAS CATO-C4X-252017)
- Brivaracetam Impurity 59 (CAS CATO-C4X-200759)
- Lefamulinum Impurity 43 (CAS CATO-C4X-304743)
- Nemonoxacin Impurity 54 (CAS 269407-02-5)
- n-(4-Nitrophenyl)-3,4-dihydro-2h-1-benzopyran-4-amine (CAS 1152610-85-9)
- 6-Bromo-3-phenyl-2,4(1H,3H)-quinazolinedione (CAS 23965-11-9)
- (S)-Methyl 3-(4-hydroxy-3-nitrophenyl)-2-(2,2,2-trifluoroacetamido)propanoate (CAS 5106-00-3)
- 4-Bromo-5-fluoro-2-hydroxybenzaldehyde (CAS 1427405-76-2)
- 3-(1-(Tert-butoxycarbonyl)-1,2,3,4-tetrahydroquinolin-6-yl)tetrahydrofuran-3-carboxylic acid (CAS 2387599-34-8)
- 1,3,2-Dioxaplumbolan-2-ylidene, 4,5-dioxo- (CAS 69657-50-7)
- Semaglutide impurity 251 (CAS CATO-C4X-2226251)
Why CATO?
- ISO 17034 accredited reference material producer (CNAS + ANAB dual accreditation)
- 130,000+ catalog items in stock, COA supplied with every batch
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