Meta phenoxy benzaldehyde process. The market was valued at USD 250 .
Meta phenoxy benzaldehyde process com 48, Hill Road, Bandra (West), Mumbai-400 050, INDIA The Meta Phenoxy Benzaldehyde Cyanohydrin (MPBAD Cyanohydrin) Market, valued at 7. located in Plot No. . Aromatic aldehydes such as benzaldehyde and formaldehyde may undergo disproportionation in concentrated alkali (Cannizaro's reaction); one molecule of the aldehyde is reduced to the corresponding alcohol and another molecule is simultaneously oxidized to the salt of a carboxylic acid. This method is short and yields a product of high purity which can be used as e. The Various Products That Can Be Produced By Using Meta-Phenoxy Benzaldehyde As An Dec 1, 2018 · Meta Phenoxy Benzaldehyde Product Details :- Description : Meta Phenoxy Benzaldehyde is a pesticide intermediate to manufacture synthetic pyrethroid insecticides Chemical Name : m-phenoxy benzaldehyde CAS Registry No: 39515-51-0 Packing :225 kg UN approved lacquered MS drums/HMHDPE drums Process for the prepn. The Various Products That Can Be Produced By Using Meta-Phenoxy Benzaldehyde As An Meta-Phenoxy Benzaldehyde is used as intermediates for manufacturing pyrethroids, dyes, pharmaceuticals, fungicides, and flavoring gents. particularly, the market requirement is very big. 5%, and stirring the mixture at a temperature of 25 DEG C to 35 DEG C for 25 minutes to 35 minutes; reducing the temperature with stirring Oct 21, 2025 · Gain in-depth insights into Meta Phenoxy Benzaldehyde Cyanohydrin (MPBAD Cyanohydrin) Market, projected to surge from XX million USD in 2024 to by 2033, expanding at a CAGR of ZZ%. recovered hexane ethylene dichloride is reused. This document describes the manufacturing process of meta-phenoxy benzaldehyde (MPBAD). for insecticides. The process is simple and gives high yields ( >60%) of high-purity (I). (I) is useful as an intermediate, e. 98; CAS Number: 39515-51-0; Linear Formula: C6H5OC6H4CHO; find related products, papers, technical documents, MSDS & more at 间苯氧基苯甲醛 39515-51-0 3-Phenoxy-benzaldehyde ￥75千克 湖北鸿福达生物科技有限公司 2025/11/20 3-苯氧基苯甲醛 询价 常州安科尔生物科技有限公司 2025/11/20 Legal status (The legal status is an assumption and is not a legal conclusion. This very Application Analysis Within the Meta Phenoxy Benzaldehyde Cyanohydrin market, the Agrochemicals application segment stands out as the largest and most dynamic, accounting for a substantial portion of the global market share in 2024. In this process n- Hexane is used as solvent along with phase transfer Catalyst. Request a quote today! META-PHENOXY-BENZALDEHYDE information, including chemical properties, structure, melting point, boiling point, density, formula, molecular weight, uses, prices 6 days ago · Access Verification For better experience, please slide to complete the verification process before accessing the web page. The main current applications of meta-phenoxy benzaldehyde are as an intermediate in producing insecticides like cypermethrin and fenvalerate, and the anti-itch drug METAPHENOXY BENZALDEHYDE (MPBD) DESCRIPTION METAPHENOXY BENZALDEHYDE is a pesticide intermediate to manufacture of synthetic Pyrethroid insecticides. Cypermethrin Technical Process Description Meta phenoxy Benzaldehyde & cypermethric acid chloride reacted with aqueous sodium cyanide in presence of a catalyst & produce Cypermethrin . ) Expired Application number AU21917/77A Other versions AU2191777A (en Inventor H. - from 1-bromo-3-dioxolanyl-benzene and phenol GrantedFR2432010A1 (en) Jul 30, 2025 · Hong-Kong Meta Phenoxy Benzaldehyde Cyanohydrin (MPBAD Cyanohydrin) Market size was valued at USD xx Billion in 2024 and is forecasted to grow at a CAGR of xx% from 2026 to 2033, reaching USD xx Aug 2, 2025 · The expansion of the Meta Phenoxy Benzaldehyde Cyanohydrin (MPBAD Cyanohydrin) market is driven by a confluence of strategic industrial developments, rising demand from end-use sectors, and Landscapes Chemical & Material Sciences (AREA) Organic Chemistry (AREA) Chemical Kinetics & Catalysis (AREA) Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA) AU21917/77A1976-02-051977-02-03Meta phenoxy-benzaldehyde ExpiredAU509272B2 (en) Meta-phenoxy Benzaldehyde (C13H10O2, 198. Its Nov 5, 2025 · The Japan Meta Phenoxy Benzaldehyde Market is led by a mix of local conglomerates and global enterprises driving innovation, efficiency, and digital transformation. 0 mm Hg Density : 20°C (by Authority YU Yugoslavia Prior art keywords obtaining meta phenoxy benzaldehyde benzaldehyde phenoxy meta Prior art date 1976-02-05 Application number YU288/77A Other languages English (en) Other versions YU28877A (en Inventor P H Rosinger A D Wood R A Sheldon Original Assignee Shell Int Research Authority YU Yugoslavia Prior art keywords obtaining meta phenoxy benzaldehyde benzaldehyde phenoxy meta Prior art date 1976-02-05 Application number YU288/77A Other languages English (en) Other versions YU28877A (en Inventor P H Rosinger A D Wood R A Sheldon Original Assignee Shell Int Research Authority YU Yugoslavia Prior art keywords obtaining meta phenoxy benzaldehyde benzaldehyde phenoxy meta Prior art date 1976-02-05 Application number YU288/77A Other languages English (en) Other versions YU28877A (en Inventor P H Rosinger A D Wood R A Sheldon Original Assignee Shell Int Research Authority YU Yugoslavia Prior art keywords obtaining meta phenoxy benzaldehyde benzaldehyde phenoxy meta Prior art date 1976-02-05 Application number YU288/77A Other languages English (en) Other versions YU28877A (en Inventor P H Rosinger A D Wood R A Sheldon Original Assignee Shell Int Research Authority YU Yugoslavia Prior art keywords obtaining meta phenoxy benzaldehyde benzaldehyde phenoxy meta Prior art date 1976-02-05 Application number YU288/77A Other languages English (en) Other versions YU28877A (en Inventor P H Rosinger A D Wood R A Sheldon Original Assignee Shell Int Research C07C45/565 — Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds from heterocyclic compounds with nitrogen as the only hetero atom by reaction with hexamethylene-tetramine YU288/77A1976-02-051977-02-03Process for obtaining meta-phenoxy benzaldehyde YU40291B (en) C07C45/565 — Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds from heterocyclic compounds with nitrogen as the only hetero atom by reaction with hexamethylene-tetramine YU288/77A1976-02-051977-02-03Process for obtaining meta-phenoxy benzaldehyde YU40291B (en) C07C45/565 — Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds from heterocyclic compounds with nitrogen as the only hetero atom by reaction with hexamethylene-tetramine YU288/77A1976-02-051977-02-03Process for obtaining meta-phenoxy benzaldehyde YU40291B (en) Authority YU Yugoslavia Prior art keywords obtaining meta phenoxy benzaldehyde benzaldehyde phenoxy meta Prior art date 1976-02-05 Application number YU288/77A Other languages English (en) Other versions YU28877A (en Inventor P H Rosinger A D Wood R A Sheldon Original Assignee Shell Int Research Authority YU Yugoslavia Prior art keywords obtaining meta phenoxy benzaldehyde benzaldehyde phenoxy meta Prior art date 1976-02-05 Application number YU288/77A Other languages English (en) Other versions YU28877A (en Inventor P H Rosinger A D Wood R A Sheldon Original Assignee Shell Int Research Authority YU Yugoslavia Prior art keywords obtaining meta phenoxy benzaldehyde benzaldehyde phenoxy meta Prior art date 1976-02-05 Application number YU288/77A Other languages English (en) Other versions YU28877A (en Inventor P H Rosinger A D Wood R A Sheldon Original Assignee Shell Int Research C07C45/565 — Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds from heterocyclic compounds with nitrogen as the only hetero atom by reaction with hexamethylene-tetramine YU288/77A1976-02-051977-02-03Process for obtaining meta-phenoxy benzaldehyde YU40291B (en) Authority YU Yugoslavia Prior art keywords obtaining meta phenoxy benzaldehyde benzaldehyde phenoxy meta Prior art date 1976-02-05 Application number YU288/77A Other languages English (en) Other versions YU28877A (en Inventor P H Rosinger A D Wood R A Sheldon Original Assignee Shell Int Research C07C45/565 — Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds from heterocyclic compounds with nitrogen as the only hetero atom by reaction with hexamethylene-tetramine YU288/77A1976-02-051977-02-03Process for obtaining meta-phenoxy benzaldehyde YU40291B (en) C07C45/565 — Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds from heterocyclic compounds with nitrogen as the only hetero atom by reaction with hexamethylene-tetramine YU288/77A1976-02-051977-02-03Process for obtaining meta-phenoxy benzaldehyde YU40291B (en) C07C45/565 — Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds from heterocyclic compounds with nitrogen as the only hetero atom by reaction with hexamethylene-tetramine YU288/77A1976-02-051977-02-03Process for obtaining meta-phenoxy benzaldehyde YU40291B (en) C07C45/565 — Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds from heterocyclic compounds with nitrogen as the only hetero atom by reaction with hexamethylene-tetramine YU288/77A1976-02-051977-02-03Process for obtaining meta-phenoxy benzaldehyde YU40291B (en) C07C45/565 — Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds from heterocyclic compounds with nitrogen as the only hetero atom by reaction with hexamethylene-tetramine YU288/77A1976-02-051977-02-03Process for obtaining meta-phenoxy benzaldehyde YU40291B (en) Authority YU Yugoslavia Prior art keywords obtaining meta phenoxy benzaldehyde benzaldehyde phenoxy meta Prior art date 1976-02-05 Application number YU288/77A Other languages English (en) Other versions YU28877A (en Inventor P H Rosinger A D Wood R A Sheldon Original Assignee Shell Int Research Authority YU Yugoslavia Prior art keywords obtaining meta phenoxy benzaldehyde benzaldehyde phenoxy meta Prior art date 1976-02-05 Application number YU288/77A Other languages English (en) Other versions YU28877A (en Inventor P H Rosinger A D Wood R A Sheldon Original Assignee Shell Int Research Authority YU Yugoslavia Prior art keywords obtaining meta phenoxy benzaldehyde benzaldehyde phenoxy meta Prior art date 1976-02-05 Application number YU288/77A Other languages English (en) Other versions YU28877A (en Inventor P H Rosinger A D Wood R A Sheldon Original Assignee Shell Int Research Authority YU Yugoslavia Prior art keywords obtaining meta phenoxy benzaldehyde benzaldehyde phenoxy meta Prior art date 1976-02-05 Application number YU288/77A Other languages English (en) Other versions YU28877A (en Inventor P H Rosinger A D Wood R A Sheldon Original Assignee Shell Int Research Authority YU Yugoslavia Prior art keywords obtaining meta phenoxy benzaldehyde benzaldehyde phenoxy meta Prior art date 1976-02-05 Application number YU288/77A Other languages English (en) Other versions YU28877A (en Inventor P H Rosinger A D Wood R A Sheldon Original Assignee Shell Int Research Authority YU Yugoslavia Prior art keywords obtaining meta phenoxy benzaldehyde benzaldehyde phenoxy meta Prior art date 1976-02-05 Application number YU288/77A Other languages English (en) Other versions YU28877A (en Inventor P H Rosinger A D Wood R A Sheldon Original Assignee Shell Int Research Authority YU Yugoslavia Prior art keywords obtaining meta phenoxy benzaldehyde benzaldehyde phenoxy meta Prior art date 1976-02-05 Application number YU288/77A Other languages English (en) Other versions YU28877A (en Inventor P H Rosinger A D Wood R A Sheldon Original Assignee Shell Int Research Process for the prepn. The market was valued at USD 250 Authority YU Yugoslavia Prior art keywords obtaining meta phenoxy benzaldehyde benzaldehyde phenoxy meta Prior art date 1976-02-05 Application number YU288/77A Other languages English (en) Other versions YU28877A (en Inventor P H Rosinger A D Wood R A Sheldon Original Assignee Shell Int Research C07C45/565 — Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds from heterocyclic compounds with nitrogen as the only hetero atom by reaction with hexamethylene-tetramine YU288/77A1976-02-051977-02-03Process for obtaining meta-phenoxy benzaldehyde YU40291B (en) Jul 26, 2025 · Stay ahead of the curve with the new Meta Phenoxy Benzaldehyde Cyanohydrin (MPBAD Cyanohydrin) Market Report, your go-to resource for in-depth industry analysis. of meta-phenoxy-benzaldehyde (IV); (b) removal of the dioxolan group by use of a strong acid to give (I). But, the cyclopropane carboxylate derivative is produced from 4-Chloro-3,3-dimethyl-2-(2,2,2-trichloroethyl)cyclobutanone. Not for medicinal, household or other use. This compound is known for its distinct odor and is often used as a fragrance ingredient in personal care products. Heat the reactor to 1000C through hot water circulation and start chlorination. CHEMICAL NAME m-phenoxy benzaldehyde CAS REGISTRY NO. Application : Benzaldehyde is used in manufacturing of Cinnamaldehyde ,Alpha Amyl Cinnamaldehyde, Cinnamic Alcohol ,Rose Crystals, Meta Phenoxy Benzaldehyde ,Malachite Green ,Congo Red, Congo Scarlet Packing & Storage: 220 Kg HDPE 57 ABSTRACT Meta-phenoxytoluene is oxidized by selenium dioxide in the presence of a dehydration agent to yield meta phenoxy-benzaldehyde containing less than 250 ppm dissolved selenium at a selectivity based on the toluene of about 90% or better. The cyclobutanone So meta-phenoxy benzaldehyde is a captive product and its economic scenario could be explained by the help of the insecticides scenarios of the synthetic pyrethroids. This on reaction with Cypermethric Acid Chloride forms the final Product Cypermethrin. The existing capacity for Meta Phenoxy Benzaldehyde is 30 MT/Month. Meta-phenoxytoluene is oxidized by selenium dioxide in the presence of a dehydration agent to yield meta-phenoxy-benzaldehyde containing less than 250 ppm dissolved selenium at a selectivity based on the toluene of about 90% or better. Wood DA. Apr 16, 2021 · Abstract The invention belongs to the technical field of organic synthesis, and particularly relates to a preparation method of m-phenoxy benzaldehyde. It is produced through the bromination of benzaldehyde and reaction with phenol. Authority YU Yugoslavia Prior art keywords obtaining meta phenoxy benzaldehyde benzaldehyde phenoxy meta Prior art date 1976-02-05 Application number YU288/77A Other languages English (en) Other versions YU28877A (en Inventor P H Rosinger A D Wood R A Sheldon Original Assignee Shell Int Research Apr 11, 2019 · ABSTRACT: The synthesis of functionalized (benz)aldehydes, via a two-step, one-pot procedure, is presented. 9 0 9 8 8 6/0559 9 0 9 8 8 6/0559 GB2055799A * 1979-08-08 1981-03-11 Prod Chim Auxil Synthese Improved method for the preparation of meta-phenoxy-benzaldehyde US4284825A * 1978-11-08 1981-08-18 Basf Aktiengesellschaft 4-Substituted benzaldehyde-dialkylacetal Family To Family Citations * Cited by examiner, † Cited by third party Meta-phenoxy Benzaldehyde (C13H10O2, 198. 7 Claims, No Drawings Authority IL Israel Prior art keywords benzaldehyde phenoxy meta preparation Prior art date 1976-02-05 Application number IL7751379A Other languages English (en) Other versions IL51379A0 (en Original Assignee Shell Int Research Jul 25, 1979 · Process for the preparation of meta- aryloxybenzaldehydes, especially meta- phenoxybenzaldehyde, which comprises reacting a mixture of meta-aryloxybenzyl and meta-aryloxybenzal halides with hexamethylenetetramine and hydrolysing the resulting pro- duct in the presence of a non-acidic solvent. P. Landscapes Chemical & Material Sciences (AREA) Organic Chemistry (AREA) Chemical Kinetics & Catalysis (AREA) Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA) AU21917/77A1976-02-051977-02-03Meta phenoxy-benzaldehyde ExpiredAU509272B2 (en) C07C45/565 — Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds from heterocyclic compounds with nitrogen as the only hetero atom by reaction with hexamethylene-tetramine AU21917/77A1976-02-051977-02-03Meta phenoxy-benzaldehyde ExpiredAU509272B2 (en) C07C45/565 — Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds from heterocyclic compounds with nitrogen as the only hetero atom by reaction with hexamethylene-tetramine AU21917/77A1976-02-051977-02-03Meta phenoxy-benzaldehyde ExpiredAU509272B2 (en) Oct 21, 2025 · Gain in-depth insights into Meta Phenoxy Benzaldehyde Cyanohydrin (MPBAD Cyanohydrin) Market, projected to surge from XX million USD in 2024 to by 2033, expanding at a CAGR of ZZ%. 5 million in 2022 and is projected to grow at a compound annual growth rate (CAGR Oct 14, 2025 · Introduction to Meta Phenoxy Benzaldehyde Meta Phenoxy Benzaldehyde is a chemical compound that belongs to the class of aromatic aldehydes. The production of Meta Phenoxy Benzaldehyde Cyanohydrin (MPBAD Cyanohydrin) faces significant supply chain challenges, primarily driven by raw material scarcity, strict regulatory compliance, and geopolitical disruptions. It can also serve as a starting material for the production of dyes, perfumes, and flavors. Landscapes Chemical & Material Sciences (AREA) Organic Chemistry (AREA) Chemical Kinetics & Catalysis (AREA) Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA) AU21917/77A1976-02-051977-02-03Meta phenoxy-benzaldehyde ExpiredAU509272B2 (en) Nov 15, 2025 · Product identifier Product name: 3-Phenoxybenzaldehyde CBnumber: CB1697209 CAS: 39515-51-0 EINECS Number: 254-487-1 Synonyms: 3-Phenoxybenzaldehyde,M-Phenoxy Benzaldehyde Relevant identified uses of the substance or mixture and uses advised against Relevant identified uses: For R&D use only. - from 1-bromo-3-dioxolanyl-benzene and phenol GrantedFR2432010A1 (en) Jul 30, 2025 · Hong-Kong Meta Phenoxy Benzaldehyde Cyanohydrin (MPBAD Cyanohydrin) Market size was valued at USD xx Billion in 2024 and is forecasted to grow at a CAGR of xx% from 2026 to 2033, reaching USD xx Aug 2, 2025 · The expansion of the Meta Phenoxy Benzaldehyde Cyanohydrin (MPBAD Cyanohydrin) market is driven by a confluence of strategic industrial developments, rising demand from end-use sectors, and The process is simple and gives high yields ( >60%) of high-purity (I). A method for the preparation of meta-phenoxy-benzaldehyde comprises reacting an excess of phenol with meta-bromo-benzaldehyde dioxolane at 200 DEG C in the presence of copper or of a copper salt and potassium carbonate, and then eliminating the dioxolane function by means of a strong acid. (I A process for the preparation of meta-phenoxy-benzaldehyde in which in the presence of copper or a copper salt and potassium carbonate at 200 0 C, a phenol excess with the dioxolane of the meta-bromo-benzaldehyde is reacted, -What then the dioxolane group by a strong acid is released. Request a quote today! Other name: Benzenecarbaldehyde, Phenylmethanal, Benzoic Aldehyde, Benzenecarbonal, Benzenecarboxaldehyde, Benzoyl hydride, Phenylformaldehyde, Benzene methylal. Meta-phenoxy benzaldehyde is an important intermediate in the manufac- ture of a group of Authority IL Israel Prior art keywords benzaldehyde phenoxy meta preparation Prior art date 1976-02-05 Application number IL7751379A Other languages English (en) Other versions IL51379A0 (en Original Assignee Shell Int Research Source high-quality Meta-phenoxy Benzaldehyde CAS Number: 39515-51-0 from Scimplify, a trusted manufacturer and distributor. 5%, and stirring the mixture at a temperature of 25 DEG C to 35 DEG C for 25 minutes to 35 minutes; reducing the temperature with stirring Prepn. Explore Landscapes Chemical & Material Sciences (AREA) Organic Chemistry (AREA) Chemical Kinetics & Catalysis (AREA) Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA) AU21917/77A1976-02-051977-02-03Meta phenoxy-benzaldehyde ExpiredAU509272B2 (en) The invention relates to a synthesis method of a cypermethrin compound. C07C45/565 — Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds from heterocyclic compounds with nitrogen as the only hetero atom by reaction with hexamethylene-tetramine AU21917/77A1976-02-051977-02-03Meta phenoxy-benzaldehyde ExpiredAU509272B2 (en) Meta Phenoxy Benzaldehyde Cyanohydrin (MPBAD Cyanohydrin) Application In Agrochemicals industries, in the manufacturing of Cypermethrin. The cyclobutanone 6 days ago · Access Verification For better experience, please slide to complete the verification process before accessing the web page. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed. The expansion project involves modifications and reconstruction of existing structures to accommodate additional production capacity. Cpd. The catalyst of the invention comprises an amount effective as cyclo- catalyst ( phenylalanyl-histidine) enantiomer adsorbed on a solid support comprising a non-ionic polymer resin Applications. of meta-phenoxy-benzaldehyde (I) by (a) reaction of a slight excess of bromo-benzene (II) with the dioxolan deriv. It is a cyclopropane carboxylate derivative which can be synthesized using 2-(2,2-dichlorovinyl)-3,3-dimethylcyclopropanecarboxylic acid chloride, sodium cyanide and meta-phenoxy benzaldehyde. g. Uses advised against: none Company Identification Company Jun 5, 2023 · Meta Phenoxy Benzaldehyde (MPBAD) is a chemical compound with the molecular formula C₆H₅CH (OH)C₆H₄O. It lists MPBD as a liquid with a colorless to yellow appearance. MPBAD Cyanohydrin is a critical intermediate in the synthesis of various pesticides, herbicides, and fungicides, which are indispensable for modern agricultural The European market for Meta Phenoxy Benzaldehyde Cyanohydrin is characterized by a mature industrial landscape with a strong emphasis on regulatory compliance and sustainable practices. to yield the dioxolan deriv. and Sheldon RA Insinger Landscapes Chemical & Material Sciences (AREA) Organic Chemistry (AREA) Chemical Kinetics & Catalysis (AREA) Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA) AU21917/77A1976-02-051977-02-03Meta phenoxy-benzaldehyde ExpiredAU509272B2 (en) ChemicalBook 为您提供间苯氧基苯甲醛 (39515-51-0)的化学性质，熔点，沸点，密度，分子式，分子量，物理性质，毒性，结构式，海关编码等信息，同时您还可以浏览间苯氧基苯甲醛 (39515-51-0)产品的价格，供应商，贸易商，生产企业和生产厂家，最后间苯氧基苯甲醛 (39515-51-0)的中文，英文，用途，CAS The process is simple and gives high yields ( >60%) of high-purity (I). 21% during 2026–2033, reaching 17. 31 billion by Aldrich-191752; 3-Phenoxybenzaldehyde 0. An improved process for the preparation of meta phenoxy benzalcleliydeAn improved process for the preparation of meta phenoxy benzaldehyde by oxidising meta phenoxy toluene in presence of a catalyst containing a mixture of a salt of cobalt and manganese i Case status Granted + Allowed to lapse Licensing status Licensing case no Client name Lead Find here online companies selling meta-phenoxy-benzaldehyde . We claim: An improved process for the preparation of meta-phenoxy benzaldehyde, comprising oxidation of meta-phenoxy toluene in presence of a catalyst containing cobalt and manganese acetates in 3-phenoxy-benzaldehyde (hereinafter to be referred as ether aldehyde) (3-Phenoxy-benzaldehyde, CAS:39515-51-0, EINECS:254-487-1) be medicine and agricultural chemicals, the important intermediate of high-efficient low toxicity insecticide pyrethroid such as Deltamethrin, Cypermethrin etc. of a m-phenoxybenzaldehyde (I) is carried out by (a) reacting 1-bromo-3- (1,3-dioxolan-2yl)benzene (II) with excess phenol at 200 degrees C. The method includes adding water to sodium cyanide and a phase transfer catalyst to stir and dissolve the mixture, adding a phenoxy-benzaldehyde solvent with a mass concentration of 98. MPBD may cause eye, skin, respiratory, and digestive tract irritation and is harmful if swallowed. A method of preparing the Aromatic aldehydes such as benzaldehyde and formaldehyde may undergo disproportionation in concentrated alkali (Cannizaro's reaction); one molecule of the aldehyde is reduced to the corresponding alcohol and another molecule is simultaneously oxidized to the salt of a carboxylic acid. Technology and Process Description Manufacturing process of each product is enclosed as Annexure I Source high-quality Meta-phenoxy Benzaldehyde CAS Number: 39515-51-0 from Scimplify, a trusted manufacturer and distributor. Hexane & ethylene dichloride is used as a solvent . The method employs a stable aluminum hemiaminal as a tetrahedral intermediate, protecting a latent aldehyde, making it suitable for subsequent cross-coupling with (strong nucleophilic) organometallic reagents, leading to a variety of alkyl and aryl substituted benzaldehydes. 22 g/mol) is an important pesticide intermediate used in the synthesis of insecticides, enhancing pest control efficiency in agricultural applications. Personal protective equipment including gloves, safety goggles, and proper ventilation should be used when handling MPBD. FR7822366A1978-07-281978-07-28Meta-phenoxy-benzaldehyde prepn. 39515-51-0 STRUCTURAL FORMULA PHYSICAL PROPERTIES Appearance : Colourless to light yellow clear liquid free from extraneous impurities. This is a novel process for the preparation of m-phenoxybenzaldehyde, a useful and valuable intermediate for the synthesis of pyrethroid type pesticides. Specification Stage 3: Preparation of Meta Phenoxy Benzaldehyde Acetal The MBBA is react with Phenol and KOH with solvent as toluene by removing the water by azeotropically with the presence of catalyst at 142 deg centigrade. 1 Uses Of Various Pesticides All Over the world: Meta-Phenoxy Benzaldehyde is used as intermediates for manufacturing pyrethroids, dyes, pharmaceuticals, fungicides, and flavoring gents. 4 billion in 2025, is anticipated to advance at a CAGR of 15. Each record includes HS Code classification, shipment value (FOB/CIF), quantity, port Authority IL Israel Prior art keywords benzaldehyde phenoxy meta preparation Prior art date 1976-02-05 Application number IL7751379A Other languages English (en) Other versions IL51379A0 (en Original Assignee Shell Int Research META-PHENOXY-BENZALDEHYDE information, including chemical properties, structure, melting point, boiling point, density, formula, molecular weight, uses, prices Abstract: Cypermethrin has a growing demand in India. It belongs to the class of organic compounds known as benzaldehydes, MPBAD is commonly used in the synthesis of various organic compounds and pharmaceutical intermediates. Available in stock at competitive prices. C07C45/565 — Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds from heterocyclic compounds with nitrogen as the only hetero atom by reaction with hexamethylene-tetramine YU288/77A1976-02-051977-02-03Process for obtaining meta-phenoxy benzaldehyde YU40291B (en) Authority YU Yugoslavia Prior art keywords obtaining meta phenoxy benzaldehyde benzaldehyde phenoxy meta Prior art date 1976-02-05 Application number YU288/77A Other languages English (en) Other versions YU28877A (en Inventor P H Rosinger A D Wood R A Sheldon Original Assignee Shell Int Research C07C45/565 — Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds from heterocyclic compounds with nitrogen as the only hetero atom by reaction with hexamethylene-tetramine YU288/77A1976-02-051977-02-03Process for obtaining meta-phenoxy benzaldehyde YU40291B (en) Authority YU Yugoslavia Prior art keywords obtaining meta phenoxy benzaldehyde benzaldehyde phenoxy meta Prior art date 1976-02-05 Application number YU288/77A Other languages English (en) Other versions YU28877A (en Inventor P H Rosinger A D Wood R A Sheldon Original Assignee Shell Int Research This document provides the material safety data sheet for meta phenoxy benzaldehyde (MPBD). We increased our capacity of meta phenoxy benzaldehyde (MPBD) and also started manufacturing CMAC, as part of backward integration that made us globally competitive for molecules like: alphacypermethrin, cypermethrin, lambdacyhalothrin, and permethrin. Boiling Point : 140°C at 1. Acetic acid is converted into Mono chloro Acetic acid in presence of suitable catalyst. with a strong acid. The information relates only to the specific material designated and may not be valid for such material used in combination with any other materials or in any process, unless specified in the text Meta-phenoxy benzaldehyde is an important agrochemical intermediate used in manufacturing synthetic pyrethroids like decamethrin and cypermethrin. May 15, 2025 · The global Meta Phenoxy Benzaldehyde Cyanohydrin (MPBAD Cyanohydrin) market was valued at approximately USD 126. Contact Metaphenoxy-benzaldehyde Home Metaphenoxy-benzaldehyde +91-22-66265600 contactus@gharda. The Various Products That Can Be Produced By Using Meta-Phenoxy Benzaldehyde As An 3-Phenoxybenzaldehyde | C13H10O2 | CID 38284 - structure, chemical names, physical and chemical properties, classification, patents, literature, biological activities Meta-Phenoxy Benzaldehyde is used as intermediates for manufacturing pyrethroids, dyes, pharmaceuticals, fungicides, and flavoring gents. of meta-hydroxy-benzaldehyde (III) at 160-200 degrees C, in the presence of copper or a copper salt and an alkaline cpd. in the presence of Cu or a Cu salt and K2CO3 and (b) cleaving the dioxolanyl gp. An improved process for the preparation of meta-phenoxy benzaldehyde, comprising oxidation of meta-phenoxy toluene in presence of a catalyst containing cobalt and Nov 29, 2000 · More particularly, the present invention relates to an improved process for the production of meta-phenoxy benzaldehyde by aerial oxidation of meta-phenoxy toluene in the presence of a mixture of transition metal salts in acetic acid as solvent, using bromide as a promoter. It also provides Authority YU Yugoslavia Prior art keywords obtaining meta phenoxy benzaldehyde benzaldehyde phenoxy meta Prior art date 1976-02-05 Application number YU288/77A Other languages English (en) Other versions YU28877A (en Inventor P H Rosinger A D Wood R A Sheldon Original Assignee Shell Int Research Authority YU Yugoslavia Prior art keywords obtaining meta phenoxy benzaldehyde benzaldehyde phenoxy meta Prior art date 1976-02-05 Application number YU288/77A Other languages English (en) Other versions YU28877A (en Inventor P H Rosinger A D Wood R A Sheldon Original Assignee Shell Int Research C07C45/565 — Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds from heterocyclic compounds with nitrogen as the only hetero atom by reaction with hexamethylene-tetramine YU288/77A1976-02-051977-02-03Process for obtaining meta-phenoxy benzaldehyde YU40291B (en) Jul 26, 2025 · Stay ahead of the curve with the new Meta Phenoxy Benzaldehyde Cyanohydrin (MPBAD Cyanohydrin) Market Report, your go-to resource for in-depth industry analysis. an intermediate for Abstract: Cypermethrin has a growing demand in India. Feb 21, 2017 · This document provides information about a proposed expansion project by M/s. However, synthesis of this important agrochemical intermediate from meta-cresol via meta-phenoxy toluene oxidation has now become commercially more attractive. During the process, HCl gas is generated, which is scrubbed through scrubber and dissolved in water to convert 30% HCl liquor. Get info on manufacturers, suppliers, & exporters lists for buying in India. Effluents will Jul 22, 2025 · Meta Phenoxy Benzaldehyde Cyanohydrin (MPBAD Cyanohydrin) Market : Key Highlights Rapid technological advancements in synthesis processes are enhancing product purity and yield, driving broader The invention relates to a catalyst and process for the asymmetric synthesis of cyanohydrin m-phenoxy-benzaldehyde. It is commonly used in various industries, including pharmaceuticals, perfumes, and agrochemicals. 3. (I Authority YU Yugoslavia Prior art keywords obtaining meta phenoxy benzaldehyde benzaldehyde phenoxy meta Prior art date 1976-02-05 Application number YU288/77A Other languages English (en) Other versions YU28877A (en Inventor P H Rosinger A D Wood R A Sheldon Original Assignee Shell Int Research It will be appreciated, therefore, that the present invention provides a valuable route to meta-phenoxy-benzaldehyde starting from meta-phenoxy-toluene without the need to isolate a particular intermediate chloride or bromide for conversion into the aldehyde. The Various Products That Can Be Produced By Using Meta-Phenoxy Benzaldehyde As An Process for the preparation of meta-aryloxybenzaldehydes, especially meta-phenoxybenzaldehyde, which comprises reacting a mixture of meta-aryloxybenzyl and meta-aryloxybenzal halides with hexamethylenetetramine and hydrolysing the resulting product in the presence of a non-acidic solvent. Its specific A B S T R A C T A process for the preparation of meta-aryloxy-benz-aldehydes, especially 3-phenoxy-benzaldehyde, which comprises reacting a mixture of the corresponding meta-aryloxy-benzyl and -benzal halides with ammonia and formaldehyde and, in a second step, hydrolyzing the resultant product under acid conditions to form the desired meta-aryloxy-benzaldehyde. 3208, Ankleshwar Industrial Area, Gujarat. Benzaldehyde is manufactured by benzaldehyde via bromination, and phenol. Here we are considering Insecticides to explain the economic scenario of meta-phenoxy benzaldehyde. Meta-phenoxy benzaldehyde is an important intermediate in the manufacture of a group of insecticidally Meta-Phenoxy Benzaldehyde is used as intermediates for manufacturing pyrethroids, dyes, pharmaceuticals, fungicides, and flavoring gents. the catalyst is particularly useful in a process for the synthesis of (s) -m-phenoxy Meta-Phenoxy Benzaldehyde is used as intermediates for manufacturing pyrethroids, dyes, pharmaceuticals, fungicides, and flavoring gents. The market was valued at USD 250 Authority YU Yugoslavia Prior art keywords obtaining meta phenoxy benzaldehyde benzaldehyde phenoxy meta Prior art date 1976-02-05 Application number YU288/77A Other languages English (en) Other versions YU28877A (en Inventor P H Rosinger A D Wood R A Sheldon Original Assignee Shell Int Research Existing 1. Gain full visibility into the global Meta Phenoxy Benzaldehyde trade with accurate and real-time Meta Phenoxy Benzaldehyde Import Data, powered by Cybex Exim Solutions Pvt. Accordingly, a particular aspect of the invention concerns a process for the preparation of meta-phenoxy-benzaldehyde which comprises: (a) preparing a mixture of meta-phenoxy-benzyl halide and meta-phenoxy-benzal halide by halogenating meta-phenoxy-toluene with gaseous halogen at an elevated temperature in the presence of a free radical initiator; Manufacturing Process: Meta Phenoxy Benzaldehyde is reacted with Sodium Cyanide to form Meta Phenoxy Benzaldehyde Cyanohydrin as an intermediate. MPBAD is an intermediate used in producing various products like insecticides, pesticides, dyes and pharmaceuticals. Our platform offers reliable and verified trade intelligence across major Meta Phenoxy Benzaldehyde exporting and importing nations. Hemani Intermediates Pvt. Ltd. fqnbqfbvpalzmrwynkatmfvxwyysvqslssjzhtaetlslqqutzfmjyaqckehgvxonvdrcovyla