2-(tert-butyl)-5-methyl-1h-indole 2-tert-butyl-5-methyl-1H-indole 69622-41-9 A9210 CAS 69622-41-9
| CAS No. | 69622-41-9 |
| Molecular Formula | C13H17N |
| Molecular Weight | 187.28 g/mol |
| Category | Pharmaceutical Standards / API Standards |
| Availability | In Stock |
Chemical Structure
Description
This reference standard is suitable for quantitative analysis on major chromatographic platforms including HPLC, GC, LC-MS/MS, and GC-MS, serving as an external calibration standard or a system suitability test reference material.
CATO supplies 2-(tert-butyl)-5-methyl-1h-indole 2-tert-butyl-5-methyl-1H-indole 69622-41-9 A9210 (CAS 69622-41-9), a certified reference material (molecular formula C13H17N, MW 187.28 g/mol) for analytical method development and quality control.
Structurally, 2-(tert-butyl)-5-methyl-1h-indole 2-tert-butyl-5-methyl-1H-indole 69622-41-9 A9210 (C13H17N) contains a nitrogen-containing heterocyclic scaffold, a nitrile group. The molecule exhibits a degree of unsaturation (DBE) of 6.0, corresponding to approximately 6 ring(s) or double-bond equivalent(s). With a molecular weight of 187.28 g/mol, it falls into the medium-molecular-weight range. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.
CATO manufactures 2-(tert-butyl)-5-methyl-1h-indole 2-tert-butyl-5-methyl-1H-indole 69622-41-9 A9210 under ISO 17034:2016 accreditation with dual CNAS and ANAB accreditation. Each batch is characterized by orthogonal methods and supplied with a full Certificate of Analysis (COA), ensuring metrological traceability.
Physical & Chemical Properties
| Molecular Formula | C13H17N |
| Molecular Weight | 187.28 g/mol |
| Purity | 97%+ |
| Storage | Store at 2-8°C, protect from light |
| Solubility (reference) | Soluble in chloroform, dichloromethane, ethyl acetate |
| Stability | Light-sensitive; avoid direct strong light |
| Degree of Unsaturation (DBE) | 6.0 |
| UV Absorption | UV-absorbing |
| Structural Features | Aromatic ring present |
| CAS Registry Year (est.) | 1976 |
| Nitrogen Atoms | 1 |
Recommended Standards
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Why CATO?
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