[9] The European Union has forbidden the use of morpholine in fruit coating.[10][11]. Some of the following links exit EPA's site [7], It is commonly used to generate enamines.[8]. Use of the information without obtaining the permission from the owner(s) of the respective information might violate the rights of the owner.

This information has not been reviewed or verified by the Agency or any other authority. Please upgrade your Internet Explorer to a newer version. Shop a large selection of products and learn more about Morpholine, 99+%, ACS reagent, ACROS Organics. [5], Morpholine is often produced industrially by the dehydration of diethanolamine with sulfuric acid:[6]. This substance exists as a Related Substance of the following substances. Morpholine is used as a chemical emulsifier in the process of waxing fruit. Systematic Name Synonym CAS Number TSN EPA Identifier Effective Date End Date; Volatile organic compounds Volatile organic compounds: E761346: 08/15/2000: Morpholine, mixt.

In research and in industry, the low cost and polarity of morpholine lead to its common use as a solvent for chemical reactions. Information on Registered Substances comes from registration dossiers which have been assigned a registration number. This table shows how each list refers to the substance. It is the formamide of morpholine … The naming of morpholine … For example, treating morpholine with hydrochloric acid makes the salt morpholinium chloride. Morpholine is an organic chemical compound having the chemical formula O(CH2CH2)2NH.

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Identifiers CAS Number. Morpholine is used because its volatility is about the same as water, so once it is added to the water, its concentration becomes distributed rather evenly in both the water and steam phases. To view more metadata about the specific Synonym, click on the Synonym. Morpholine derivatives used as agricultural fungicides in cereals are known as ergosterol biosynthesis inhibitors. Names Preferred IUPAC name.

Morpholine is often used in conjunction with low concentrations of hydrazine or ammonia to provide a comprehensive all-volatile treatment chemistry for corrosion protection for the steam systems of such plants. This heterocycle features both amine and ether functional groups. Naturally, fruits make waxes to protect against insects and fungal contamination, but this can be lost as the fruit is cleaned. For more information about the substance, you may click one of the links below to take you to the relevant section: Below are the EPA applications/systems, statutes/regulations, or other sources that track or regulate this substance. 4394-85-8; 3D model . Contact Us to ask a question, provide feedback, or report a problem. EPA Registry Name: Morpholine. For this reason, it forms a stable chloramine. Welcome to the ECHA website.

For example, treating morpholine with hydrochloric acid makes the salt morpholinium chloride. Except where otherwise noted, data are given for materials in their, National Institute for Occupational Safety and Health, "4-Chlorination of Electron-Rich Benzenoid Compounds: 2,4-Dichloromethoxybenzene", "Cyclopentenones from α,α′-Dibromoketones and Enamines: 2,5-Dimethyl-3-Phenyl-2-Cyclopenten-1-one", "Morpholine Issues in the United Kingdom", https://en.wikipedia.org/w/index.php?title=Morpholine&oldid=986497527, Pages using collapsible list with both background and text-align in titlestyle, Articles containing unverified chemical infoboxes, Creative Commons Attribution-ShareAlike License, This page was last edited on 1 November 2020, at 06:43. Morpholine-4-carbaldehyde. IUPAC Name: Morpholine CAS Number: 110-91-8. United States Environmental Protection Agency, Some of the following links exit EPA's site, Program and regulatory information about this substance, including links to EPA applications/systems, statues/regulations, or other sources that track or regulate this substance, Single Substance Request (CDX Query Function) (REST and SOAP), Substance List Request (CDX Solicit Function) (SOAP), Add Substance to List Request (CDX Submit Function) (SOAP). Display Name: Morpholine EC Number: 203-815-1 EC Name: Morpholine CAS Number: 110-91-8 Molecular formula: C4H9NO IUPAC Name: morpholine Morpholine is a common additive, in parts per million concentrations, for pH adjustment in both fossil fuel and nuclear power plant steam systems.

p-Isoxazine, tetrahydro- … Its pH-adjusting qualities then become distributed throughout the steam plant to provide corrosion protection.

EC number: 203-815-1 | CAS number: 110-91-8. Morpholine is an organic chemical compound having the chemical formula O(C H 2 CH 2) 2 NH. Email: info@alfa-chemistry.com Tel:1-201-478-8534 1-516-662-5404 Fax: 1-516-927-0118 Address: 2200 Smithtown Avenue, Room 1 Ronkonkoma, NY 11779-7329 USA For product inquiries, please use our … This heterocycle features both amine and ether functional groups.Because of the amine, morpholine is a base; its conjugate acid is called morpholinium. A small amount of new wax is applied to replace it. with sodium hydroxide Morpholine… ... Morpholine (8CI, 9CI) Registration dossier . Because of the amine, morpholine is a base; its conjugate acid is called morpholinium. Morpholine decomposes reasonably slowly in the absence of oxygen at the high temperatures and pressures in these steam systems.

For example, it is a building block in the preparation of the antibiotic linezolid, the anticancer agent gefitinib (Iressa) and the analgesic dextromoramide. Particle size distribution (Granulometry), Solubility in organic solvents / fat solubility, Stability in organic solvents and identity of relevant degradation products, Storage stability and reactivity towards container material, Biodegradation in water and sediment: simulation tests, Additional information on environmental fate and behaviour, Short-term toxicity to aquatic invertebrates, Long-term toxicity to aquatic invertebrates, Toxicity to aquatic algae and cyanobacteria, Toxicity to aquatic plants other than algae, Endocrine disrupter testing in aquatic vertebrates – in vivo, Toxicity to soil macroorganisms except arthropods, Endocrine disrupter mammalian screening – in vivo (level 3), Direct observations: clinical cases, poisoning incidents and other, Exposure related observations in humans: other data, Additional physico-chemical properties of nanomaterials, Toxicokinetics, metabolism and distribution. 5g; Glass bottle. The assignment of a registration number does however not guarantee that the information in the dossier is correct or that the dossier is compliant with Regulation (EC) No 1907/2006 (the REACH Regulation). This site is not fully supported in Internet Explorer 7 (and earlier versions). There is no structure for this substance. The naming of morpholine is attributed to Ludwig Knorr, who incorrectly believed it to be part of the structure of morphine. Morpholine undergoes most chemical reactions typical for other secondary amines, though the presence of the ether oxygen withdraws electron density from the nitrogen, rendering it less nucleophilic (and less basic) than structurally similar secondary amines such as piperidine. Morpholine is widely used in organic synthesis. Use of this information is subject to copyright laws and may require the permission of the owner of the information, as described in the ECHA Legal Notice. This website uses cookies to ensure you get the best experience on our websites. The following list includes links related to the selected substance. Exit. Morpholine is used as an emulsifier and solubility aid for shellac, which is used as a wax for fruit coating.

Regulatory process names 18 Translated names 24 CAS names 1 IUPAC names 12 Trade names 14 Other identifiers 14 . The content is subject to change without prior notice.Reproduction or further distribution of this information may be subject to copyright protection. Other names Formylmorpholine 4-Morpholinecarboxaldehyde.

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