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· · COA & SDS available for every product · Same-day shipping on in-stock items 4-(Pentafluorothio)aniline - ≥95%(GC) , CAS No.2993-24-0
Synonyms
GS-5429 | STL555346 | SB77202 | MFCD01076203 | 4-Aminobenzenesulfur pentafluoride | AKOS005254366 | F0001-0923 | 4-(pentafluoro-lambda6-sulfanyl)aniline | SCHEMBL240645 | A903312 | EN300-129955 | 1-AMINO-4-(PENTAFLUORO-SULFANYL)BENZENE | C6H6F5NS | MZGZUH
Storage
Store at 2-8°C,Argon charged
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Why this grade ≥95%(GC) for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Store at 2-8°C,Argon charged Ships Wet ice 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 Synonyms
GS-5429 | STL555346 | SB77202 | MFCD01076203 | 4-Aminobenzenesulfur pentafluoride | AKOS005254366 | F0001-0923 | 4-(pentafluoro-lambda6-sulfanyl)aniline | SCHEMBL240645 | A903312 | EN300-129955 | 1-AMINO-4-(PENTAFLUORO-SULFANYL)BENZENE | C6H6F5NS | MZGZUH
Specifications & Purity
≥95%(GC)
Storage
Store at 2-8°C, Argon charged
Shipped In
Wet ice
This product requires cold chain shipping. Ground and other economy services are not available.
Names and Identifiers Pubchem Sid 504762027 Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/504762027 Canonical Smiles C1=CC(=CC=C1N)S(F)(F)(F)(F)F IUPAC Name 4-(pentafluoro-λ6-sulfanyl)aniline InChIKey MZGZUHNSMNNSRJ-UHFFFAOYSA-N INCHI 1S/C6H6F5NS/c7-13(8,9,10,11)6-3-1-5(12)2-4-6/h1-4H,12H2 Isomeric SMILES C1=CC(=CC=C1N)S(F)(F)(F)(F)F PubChem CID 2779190 Molecular Weight 219.17 Reaxy-Rn 2694823
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 Benzenoids Class Benzene and substituted derivatives Subclass Aniline and substituted anilines Intermediate Tree Nodes Not available Direct Parent Aniline and substituted anilines Alternative Parents Primary amines Organosulfur compounds Organopnictogen compounds Hydrocarbon derivatives Molecular Framework Aromatic homomonocyclic compounds Substituents Aniline or substituted anilines - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Primary amine - Organosulfur compound - Organonitrogen compound - Amine - Aromatic homomonocyclic compound Description This compound belongs to the class of organic compounds known as aniline and substituted anilines. These are organic compounds containing an aminobenzene moiety. 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 Structure Certificates（CoA,COO,BSE/TSE and Analysis Chart) Chemical and Physical Properties Solubility Soluble in Methanol Sensitivity Light, air and heat sensitive Melt Point(°C) 64 °C Molecular Weight 219.180 g/mol XLogP3 4.500 Hydrogen Bond Donor Count 1 Hydrogen Bond Acceptor Count 6 Rotatable Bond Count 0 Exact Mass 219.014 Da Monoisotopic Mass 219.014 Da Topological Polar Surface Area 27.000 Ų Heavy Atom Count 13 Formal Charge 0 Complexity 200.000 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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