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224,000+ Forschungsprodukte · Triple ISO certified · COA & SDS für jedes Produkt verfügbar · Versand am selben Tag für Lagerartikel 9-Methylacridine - ≥96%(GC) , CAS No.611-64-3
Synonyms
FT-0762093 | 9-methyl acridine | Q27252344 | CARBAMAZEPINE IMPURITY B [IP] | 9-Methylacridine | 9-Methyl-acridine | BRN 0133084 | 1F3Q4U9UIS | WLN: T C666 BNJ I1 | 9-Methylakridin [Czech] | ACRIDINE, 9-METHYL- | 5-20-08-00253 (Beilstein Handbook Reference
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Why this grade ≥96%(GC) for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Room temperature Ships Normal Check lot-specific COA for exact specifications.
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Quality documents SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
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Literature proof Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Specifications Synonyme
FT-0762093 | 9-methyl acridine | Q27252344 | CARBAMAZEPINE IMPURITY B [IP] | 9-Methylacridine | 9-Methyl-acridine | BRN 0133084 | 1F3Q4U9UIS | WLN: T C666 BNJ I1 | 9-Methylakridin [Czech] | ACRIDINE, 9-METHYL- | 5-20-08-00253 (Beilstein Handbook Reference
Spezifikationen & Reinheit
≥96%(GC)
Namen und Kennungen Pubchem Sid Url
https://pubchem.ncbi.nlm.nih.gov/substance/504752219
Kanonisches Lächeln
CC1=C2C=CC=CC2=NC3=CC=CC=C13
IUPAC Name
9-methylacridine
InChIKey
FLDRLXJNISEWNZ-UHFFFAOYSA-N
INCHI
1S/C14H11N/c1-10-11-6-2-4-8-13(11)15-14-9-5-3-7-12(10)14/h2-9H,1H3
Isomere SMILES
CC1=C2C=CC=CC2=NC3=CC=CC=C13
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=133084&ln=
Documentation 📋 Safety Data Sheet (SDS) Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS → ✅ Certificate of Analysis (COA) Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA → 📊 Datasheet Quick-reference summary of product specifications and applications.
View datasheet → 🔬 Specification Sheet Full quality attributes and acceptance criteria for this grade.
View spec sheet →
Advanced Data Taxonomic Classification Kingdom Organic compounds Superclass Organoheterocyclic compounds Klasse Quinolines and derivatives Subclass Benzoquinolines Intermediate Tree Nodes Not available Direct Parent Acridines Alternative Parents Methylpyridines Benzenoids Heteroaromatic compounds Azacyclic compounds Organopnictogen compounds Organonitrogen compounds Hydrocarbon derivatives Molecular Framework Aromatic heteropolycyclic compounds Substituents Acridine - Methylpyridine - Benzenoid - Pyridine - Heteroaromatic compound - Azacycle - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Organonitrogen compound - Aromatic heteropolycyclic compound Beschreibung This compound belongs to the class of organic compounds known as acridines. These are organic compounds containing the acridine moiety, a linear tricyclic heterocycle which consists of two benzene rings joined by a pyridine ring. External Descriptors Not available Data sources 1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.
3D-Struktur Zugehörige Ziele (menschlich) Zugehörige Ziele (nicht menschlich) Wirkungsmechanismen Zertifikate (CoA, COO, BSE/TSE und Analyse-Diagramm) Chemische und physikalische Eigenschaften Schmelzpunkt (°C) 117 °C Molekulargewicht 193.240 g/mol XLogP3 3.900 Hydrogen Bond Donor Count 0 Hydrogen Bond Acceptor Count 1 Rotatable Bond Count 0 Exact Mass 193.089 Da Monoisotopic Mass 193.089 Da Topological Polar Surface Area 12.900 Ų Heavy Atom Count 15 Formal Charge 0 Complexity 203.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 0 Undefined Atom Stereocenter Count 0 Defined Bond Stereocenter Count 0 Undefined Bond Stereocenter Count 0 The total count of all stereochemical bonds 0 Covalently-Bonded Unit Count 1
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