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· · COA & SDS available for every product · Same-day shipping on in-stock items Sodium 2,4-Dinitrobenzenesulfonate - ≥98%(HPLC)(T) , CAS No.885-62-1
Synonyms
DTXSID8061262 | NSC 10377 | AKOS015912517 | Sodium 2,4-dinitrobenzenesulphonate | 2,4-Dintrobenzenesulfonicacidsodiumsalt | Benzenesulfonic acid, 2,4-dinitro-, sodium salt (1:1) | AI3-09049 | D0821 | Sodium 2,4-dinitrobenzenesulfonate | WPT7E329JW | 2,4-D
Storage
Argon charged,Room temperature
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Why this grade ≥98%(HPLC)(T) for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Argon charged,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.
Overview Application:
2,4-Dinitrobenzenesulfonic acid sodium salt is used in the synthesis of aromatic dimethylene spacer-inserted cyclodextrin derivatives.
Specifications Synonyms
DTXSID8061262 | NSC 10377 | AKOS015912517 | Sodium 2, 4-dinitrobenzenesulphonate | 2, 4-Dintrobenzenesulfonicacidsodiumsalt | Benzenesulfonic acid, 2, 4-dinitro-, sodium salt (1:1) | AI3-09049 | D0821 | Sodium 2, 4-dinitrobenzenesulfonate | WPT7E329JW | 2, 4-D
Specifications & Purity
≥98%(HPLC)(T)
Storage
Argon charged, Room temperature
Names and Identifiers Canonical Smiles C1=CC(=C(C=C1[N+](=O)[O-])[N+](=O)[O-])S(=O)(=O)[O-].[Na+] IUPAC Name sodium;2,4-dinitrobenzenesulfonate InChIKey GSBYVRKLPCSLNV-UHFFFAOYSA-M INCHI 1S/C6H4N2O7S.Na/c9-7(10)4-1-2-6(16(13,14)15)5(3-4)8(11)12;/h1-3H,(H,13,14,15);/q;+1/p-1 Isomeric SMILES C1=CC(=C(C=C1[N+](=O)[O-])[N+](=O)[O-])S(=O)(=O)[O-].[Na+] WGK Germany 3 PubChem CID 70168 Molecular Weight 270.15 Beilstein 6676810 Reaxy-Rn 6676807
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 Benzenesulfonic acids and derivatives Intermediate Tree Nodes Not available Direct Parent p-Nitrobenzenesulfonates Alternative Parents p-Bromobenzenesulfonates Nitrobenzenes Benzenesulfonyl compounds 1-sulfo,2-unsubstituted aromatic compounds Nitroaromatic compounds Sulfonyls Organosulfonic acids Propargyl-type 1,3-dipolar organic compounds Organic oxoazanium compounds Organopnictogen compounds Organonitrogen compounds Organic sodium salts Organic oxides Hydrocarbon derivatives Molecular Framework Aromatic homomonocyclic compounds Substituents P-nitrobenzenesulfonate - P-bromobenzenesulfonate - Arylsulfonic acid or derivatives - Nitrobenzene - Benzenesulfonyl group - 1-sulfo,2-unsubstituted aromatic compound - Nitroaromatic compound - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Organosulfonic acid - Sulfonyl - C-nitro compound - Organic nitro compound - Organic oxoazanium - Organic alkali metal salt - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Allyl-type 1,3-dipolar organic compound - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Organosulfur compound - Organonitrogen compound - Organic sodium salt - Organic salt - Organic oxygen compound - Organopnictogen compound - Aromatic homomonocyclic compound Description This compound belongs to the class of organic compounds known as p-nitrobenzenesulfonates. These are benzenesulfonic acids (or derivative thereof) carrying a nitro group at the para- position. External Descriptors organic sodium salt 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 water; Soluble in Methanol Sensitivity Hygroscopic Molecular Weight 270.150 g/mol XLogP3 Hydrogen Bond Donor Count 0 Hydrogen Bond Acceptor Count 7 Rotatable Bond Count 0 Exact Mass 269.956 Da Monoisotopic Mass 269.956 Da Topological Polar Surface Area 157.000 Ų Heavy Atom Count 17 Formal Charge 0 Complexity 375.000 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 2
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