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on behalf of the United States of America. Database and to verify that the data contained therein have been selected on the basis of sound scientific judgment. EC number: 202-708-7 | CAS number: 98-86-2. These in turn are used in perfume. Acetophenone is an allowed IUPAC name So is methyl phenyl ketone. Technology, Office of Data Display Name: Acetophenone EC Number: 202-708-7 EC Name: Acetophenone CAS Number: 98-86-2 Molecular formula: C8H8O IUPAC Name: 1-phenylethan-1-one To use all functions of this page, please activate cookies in your browser.
InChI=1S/C8H8O/c1-7(9)8-5-3-2-4-6-8/h2-6H,1H3, National Institute of Standards and the Standard Reference Data Act. Your institution may already be a subscriber. such sites. This service is an Elixir Core Data Resource.
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InChI=1S/C8H8O/c1-7(9)8-5-3-2-4-6-8/h2-6H,1H3, National Institute of Standards and infrared reference spectra collection. 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.
At one time it was used as a hypnotic under the name of hypnone. Select a region with data to zoom. Your institution may already be a subscriber.
in this collection were collected can be found
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All rights reserved. Find compounds which contain this structure, Find compounds which resemble this structure, European Molecular Acetophenone Acetophenone IUPAC name 1-phenylethanone Other names Phenyl methyl ketone Identifiers CAS number 98-86-2 SMILES O=C(C)C1=CC=CC=C1 InChI my.chemeurope.com With an accout for my.chemeurope.com available for this spectrum and, therefore, molar absorptivity Information on Registered Substances comes from registration dossiers which have been assigned a registration number. Biology Laboratory.
errors or omissions in the Database. uses its best efforts to deliver a high quality copy of the (e.g., DIGITIZED BY NIST FROM HARD COPY (FROM TWO SEGMENTS). © 1997-2020 LUMITOS AG, All rights reserved, https://www.chemeurope.com/en/encyclopedia/Acetophenone.html, Your browser is not current. IUPAC Standard InChIKey: KWOLFJPFCHCOCG-UHFFFAOYSA-N CAS Registry Number: 98-86-2 Chemical structure: This structure is also available as a 2d Mol file or as a computed 3d SD file The 3d structure may be viewed or Name Formula IUPAC identifier CAS number More options NIST Data SRD Program Office of Data and Informatics About FAQ Credits More documentation Acetophenone Formula: C …
A methyl ketone that is acetone in which one of the methyl groups has been replaced by a phenyl group. Copyright for NIST Standard Reference Data is governed by Use of the information without obtaining the permission from the owner(s) of the respective information might violate the rights of the owner. Acetophenone is currently listed as a Group D carcinogen indicating that it does not produce carcinogenic effects in humans. 1.) NIST Standard Reference click the mouse on the plot to revert to the orginal display.
This information has not been reviewed or verified by the Agency or any other authority. by the U.S. Secretary of Commerce on behalf of the U.S.A. In a 1994 report released by five top cigarette companies, acetophenone was listed as one of the 599 additives to cigarettes.. shall not be liable for any damage that may result from (hardcopy) spectrum. with the development of data collections included in Notice: Concentration information is not
Copyright for NIST Standard Reference Data is governed by shall not be liable for any damage that may result from Currently acetophenone mainly comes as a by-product of the phenol-acetone synthesis in the cumene oxidation process. intended to imply recommendation or endorsement by the National This chemical may be obtained by the dry distillation of a mixture of the calcium salts of acetic and benzoic acids. and HTML 5 enabled browser. With an accout for my.chemeurope.com you can always see everything at a glance – and you can configure your own website and individual newsletter. © 2018 by the U.S. Secretary of Commerce It's IUPAC names ara: Acetophenone 1-phenyl ehthanone plz plz mark as brainliest ans plz zumba12 zumba12 IUPAC name of is 1-Phenylethanone. © 2018 by the U.S. Secretary of Commerce
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NIST subscription sites provide data under the and Informatics, X-ray Photoelectron Spectroscopy Database, version 4.1, NIST / TRC Web Thermo Tables, professional edition (thermophysical and thermochemical data). ChEBI Name acetophenone ChEBI ID CHEBI:27632 Definition A methyl ketone that is acetone in which one of the methyl groups has been replaced by a phenyl group. Property Name Property Value Reference; Molecular Weight: 136.15 g/mol: Computed by PubChem 2.1 (PubChem release 2019.06.18) XLogP3: 1.4: Computed by XLogP3 3.0 (PubChem release 2019.06.18) It can be found naturally in apple, cheese, apricot, banana, beef and cauliflower. It is used in chewing gum. Find out how LUMITOS supports you with online marketing. EMBL-EBI, Wellcome Genome Campus, Hinxton, Cambridgeshire, CB10
Institute of Standards and Technology, nor is it intended to imply All rights reserved. NIST Standard Reference Acetophenone is used to create fragrances that resemble almond, cherry, honeysuckle, jasmine, and strawberry. Go To: Top, Infrared Spectrum, References. The following components were used in generating the plot: Additonal code used was developed at NIST: (.
kg−1 (LD50, Ratte, oral) Soweit möglich und gebräuchlich, werden SI-Einheiten verwendet. The name 'acetophenone' does not follow conventional IUPAC naming methods, because it is such a simple ketone it is known by the common name of acetophenone. The purpose of the fee is to recover costs associated 1SD, UK +44 (0)1223 49 44 44, Copyright © EMBL-EBI 2018 | EBI is an outstation of the European Molecular Enter the desired X axis range View scan of original
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However, NIST makes no warranties to that effect, and NIST the According to IUPAC convention, prefix eath is used for two carban and suffix one is used for functional group ketone.
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