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Benzenesulfonic Esters. PubChem Substance ID: 24868428. Only a co-crystal of the title compound with tris-(2,4,6-trimethylphenyl)stibane(V) oxide is apparent in the literature . Hazards. It has been known since at least the … Benzenesulfonic acid Formula: C 6 H 6 O 3 S Molecular weight: 158.S 3 O 8 H 7 C :)noitatoN lliH( alumroF laciripmE . Benzenesulfonic acid is an aryl sulfonic acid that can be used to form an organic salt with 5,7-dimethyl-1,8-naphthyridine-2-amine, that can be a synthon for developing supramolecular structures. Copy Sheet of paper on top of another sheet. Write a review. General Characteristics of Benzenesulfonic Acid Derivatives. Pricing and availability is not currently available.003769 Da.034 per hour, and a half-life of 170-180 hours using a electrolytic respirometer in water indicating that it is biodegraded partially in a long time by acclimatized microorganisms(4,5). Synonyms: Benzenesulfonic acid. Molecular Weight: 172. Sulfonation is a reversible reaction that produces benzenesulfonic acid by adding sulfur trioxide and fuming sulfuric acid. CAS 98-11-3.dica cinoflusenezneB :smynonyS . It is also used as a sulfonating agent to introduce sulfonic acid (SO3H) groups into organic compounds, which can be useful in the synthesis of Benzenesulfonic acid monohydrate. 2.2 kJ mol −1). Pricing and availability is not currently available. Nov 3, 1998 · Benzenesulfonic acid is an aryl sulfonic acid that can be used to form an organic salt with 5,7-dimethyl-1,8-naphthyridine-2-amine, that can be a synthon for developing supramolecular structures. Deliquescent needles or large plates. Molecular Weight 158. General Properties. Chemical structure: This structure is also available as a 2d Mol file Other names: Benzenemonosulfonic acid; Benzenesulphonic acid; Besylic acid; Phenylsulfonic acid; Kyselina benzensulfonova Permanent link for this species. Size: 0. C6H5SO3H.175 IUPAC Standard InChI: InChI=1S/C6H6O3S/c7-10 (8,9)6-4-2-1-3-5-6/h1-5H, (H,7,8,9) Copy … Dec 5, 2020 · Benzenesulfonic acid Preparation. MMYOMAG. Benzenesulfonic acid MSDS (material safety data sheet) or SDS, CoA and CoQ, dossiers, brochures and other available documents. Empirical Formula (Hill Notation): C7H8O3S. CAS Number: 98-11-3.0% (T); CAS Number: 98-11-3; Linear Formula: C6H5SO3H; find related products, papers, technical documents, MSDS & more … Nov 3, 1998 · Benzenesulfonic acid is an aryl sulfonic acid that can be used to form an organic salt with 5,7-dimethyl-1,8-naphthyridine-2-amine, that can be a synthon for developing supramolecular structures. Surprisingly, the crystal and molecular structures of benzenesulphonic acid have not been reported as of today. Molecular weight: 158.31 mm. 1. Table 1 contains crystallographic data and Table 2 contains the list of the atoms including atomic coordinates and displacement parameters. Beilstein: 742513. Size: 0. To make Benzenesulfonic acid in the laboratory, take a mixture of one part banzene and two parts concentrated sulfuric acid in a round bottom flask. : 98-11-3 1.8.175 Da; Monoisotopic mass 158.svired lykla-31-01C-onom ,dica cinoflusenezneB rof 983782274 DIS drocer ecnatsbuS .4. The sodium salt is used to standardize dyes. [1] It can also act as a dopant for the polymerization of pyrrole to form poly (pyrrole), a conducting polymer useful in the development of … 2 days ago · Benzenesulfonic acid methyl ester, Benzenesulfonic acid, methyl ester, Methyl benzenesulphonate, Methyl besylate, methyl ester of benzenesulphonic acid. To produce benzenesulfonic acid from benzene, fuming sulfuric acid and sulfur trioxide are added. Ask a question. 2. Benzenesulfonic Acid. EC Number: 201-256-8. The fusion of benzene sulfonic acid (obtained from sulfonation of benzene) with sodium hydroxide at high temperatures is one of the oldest methods for the preparation of phenol, reported separately by Kekulé < 1866MI 213-01 > and Wurtz < 1867LA (144)121 >. Sulfonic acids are strong acids. To produce benzenesulfonic acid from benzene, fuming sulfuric acid and sulfur trioxide are added.1. It has been known since at least the 1880s; its synthesis, which goes back to 1916, is via the reaction of benzene with hot concentrated sulfuric acid. Laboratory Method. Information on this page: Reaction thermochemistry data Aldrich-448737; Benzenesulfonic acid monohydrate 0.The sulfur in sulfur trioxide is electrophilic because the oxygens pull electrons away from it because oxygen is very electronegative. 705578-5MG-PW. Linear Formula: C6H5SO3H. PL860-CGA/SHF.9. The nitronium ion (NO 2+) and sulfur trioxide (SO 3) are the electrophiles and individually react with benzene to give nitrobenzene and benzenesulfonic acid respectively. CAS 98-11-3.1 Introduction. For this, benzene is heated with concentrated Sulfuric acid. Aug 29, 2023 · Benzenesulfonic acid is mainly consumed by conversion to other specialty chemicals. The interaction between benzenesulfonic acid (1) and protonated methanol cation (10) leads to the formation of a hydrogen-bonded complex (11), which is favored in gas phase (−119.2. NACRES: NA.19.3. (NTP, 1992) Health Hazard. 1,3-Benzenedisulfonic Acid. MDL number: MFCD00149976. Oct 14, 2023 · Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
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175 Da. To produce benzenesulfonic acid from benzene, fuming sulfuric acid and sulfur trioxide are added. Deliquescent needles or large plates. C 6 H 6 + H 2 SO 4 (concentrated) → C 6 H …
Benzenesulfonic acid biodegraded with a lag time of 100-110 hours, a rate of 0. Benzenesulfonic acid is used as an acid catalyst. It can also act as a dopant for the polymerization of pyrrole to form poly(pyrrole), a conducting polymer useful in the development of flexible
Jan 23, 2023 · Page ID.39 × 0.
The product is benzenesulfonic acid. Monoisotopic mass 158. It is highly water-soluble and a strong acid with a p Ka of –2.8. 1. It is the simplest aromatic sulfonic acid.
Benzenesulfonic acid methyl ester, Benzenesulfonic acid, methyl ester, Methyl benzenesulphonate, Methyl besylate, methyl ester of benzenesulphonic acid.
Benzenesulfonic acid. The sulfur in sulfur trioxide is electrophilic because the oxygens pull electrons away from it because oxygen is very
Sulfonation of Benzene. 2.39 × 0.
Benzenesulfonic acid (conjugate base benzenesulfonate) is the simplest aromatic sulfonic acid, that is soluble in water and ethanol, slightly soluble in benzene and insoluble in nonpolar solvents like diethyl ether. 3 Chemical and Physical Properties.
General Description. Browse Benzenesulfonic acid and related products at MilliporeSigma.59 × 0. (NTP, 1992) Belongs to the Following Reactive Group(s) Acids, Strong Oxidizing; Potentially Incompatible Absorbents. They are commonly cited as being around a million times stronger than the corresponding carboxylic acid. Sulfonation is a reversible reaction that produces benzenesulfonic acid by adding sulfur trioxide and fuming sulfuric acid. Information on this page:
To produce benzenesulfonic acid from benzene, fuming sulfuric acid and sulfur trioxide are added. Fuming sulfuric acid, also refered to as oleum, is a concentrated solution of dissolved sulfur trioxide in sulfuric acid.97; CAS Number: 26158-00-9; Linear Formula: C6H5SO3H · H2O; find related products, papers, technical documents, MSDS & more at Sigma-Aldrich. For this, benzene is heated with concentrated Sulfuric acid.
Mechanism., potassium salts submitted by EPA DSSTox. The alkali metal salt of benzenesulfonic acid was once widely used in the production of phenol.20. - Find MSDS or SDS, a COA, data sheets and more information.Benzenesulfonic acid ( conjugate base benzenesulfonate) is an organosulfur compound with the formula C 6 H 6 O 3 S.175; Other names: Benzenemonosulfonic acid; Benzenesulphonic acid; Besylic acid; Phenylsulfonic acid; Kyselina benzensulfonova Permanent link for this species. Individual Benzenesulfonic Acids and Derivatives.0% (T) Synonym (s): Phenylsulfonic acid.31 mm. The reaction is reversed by adding hot aqueous acid to benzenesulfonic acid to produce benzene. ChemSpider ID 7093. 2. Use this link for bookmarking this species for future reference. It is highly water-soluble and a strong acid with a p Ka of –2.serutcurtS 1 dicA cinoflusenezneB
erom eeS … ralopnon ni elbulosni dna enezneb ni elbulos ylthgils ,lonahte dna retaw ni elbulos si taht dilos yxaw etihw a ro slatsyrc teehs tnecseuqiled etihw smrof tI . 2. 98-11-3, EC Number 202-638-7. Ask a question. Browse Benzenesulfonic acid and related products at MilliporeSigma.59 × 0. SYMPTOMS: This material causes corrosion of tissues on contact.013-0. 98.
The molecular structure is shown in the figure. 98. Fuming sulfuric acid, also refered to as oleum, is a concentrated solution of dissolved sulfur trioxide in sulfuric acid. IUPAC Standard InChI: InChI=1S/C6H6O3S/c7-10 (8,9)6-4-2-1-3-5-6/h1-5H, (H,7,8,9) Copy Sheet of paper on top of another sheet.
Acid-catalyzed Ad–E pathway Results on the acid-catalyzed Ad–E mechanism are shown in Fig.175. Synonyms: Benzenesulfonic acid. [1] It can also act as a dopant for the polymerization of pyrrole to form poly (pyrrole), a conducting polymer useful in the development of flexible
Benzenesulfonic acid. 19 The possible hydrogen bond donation from methanol (2) was considered, though the resulting complex (3) is disfavored in Gibbs free energy terms.1. Recommended Products. Deliquescent needles or large plates. C 6 H 6 + H 2 SO 4 (concentrated) → C 6 H 5 SO 3 H + H 2 O.The sulfur in sulfur trioxide is electrophilic because the oxygens pull electrons away from it because oxygen is very electronegative.oN eugolataC 53621 : rebmuN tcudorP dica cinoflusenezneB : eman tcudorP
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Benzenesulfonic acid is the simplest aromatic sulfonic acid.18.0% (T) Synonym (s): Phenylsulfonic acid. All Rights Reserved.
Benzenesulfonic acid. C6H5SO3H.9. MITSCHERLICH in 1834 by heating benzene with fuming sulfuric acid. [1] It can also act as a dopant for the polymerization of pyrrole to form poly (pyrrole), a conducting polymer useful in the development of …
Aug 29, 2023 · Visit ChemicalBook To find more Benzenesulfonic acid(98-11-3) information like chemical properties,Structure,melting point,boiling point,density,molecular formula,molecular weight, physical properties,toxicity information,customs codes. It is important to note that the chemical formula of the sulfonic group is -SO 3 H. Benzenesulfonic acid is obtained from sulphonation of benzene. Fuming sulfuric acid, also refered to as oleum, is a concentrated solution of dissolved sulfur trioxide in sulfuric acid.
Benzenesulfonic acid (conjugate base benzenesulfonate) is an organosulfur compound with the formula C6H6O3S. Aldrich-12635; Benzenesulfonic acid 98. Flash point data for this chemical are not available, however it is probably combustible.
Dec 5, 2020 · Laboratory Method. Fire Hazard. Molecular Weight: 158.
Sulfonation of Benzene. 3 Chemical and Physical Properties. (NTP, 1992)
Acid hydrolysis at 175 C splits it into benzene and sulfuric acid. Formula: C 6 H 6 O 3 S; Molecular weight: 158. 2. CAS No.
Mechanism.] for compounds that feature free parapara-toluenesulphonic acid.8 and −1.9, respectively, while those of benzoic acid and acetic acid are 4.dica cinoflus citamora tselpmis eht si tI . Write a review. Copyright © 2009-2023 John Wiley & Sons, Inc.sedimanoflusenezneB .