About: 2,2,4,4-Tetramethyl-1,3-cyclobutanediol

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About: 2,2,4,4-Tetramethyl-1,3-cyclobutanediol Goto Sponge NotDistinct Permalink

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2,2,4,4-Tetramethyl-1,3-cyclobutanediol (CBDO) is an aliphatic diol. This diol is produced as a mixture of cis- and trans-isomers, depending on the relative stereochemistry of the hydroxyl groups. It is used as a monomer for the synthesis of polymeric materials. CBDO is currently being researched as an alternative to bisphenol A (BPA). BPA is a precursor used in the production of a wide range of polymers including polycarbonates, polyesters, polysulfones, and polyester ketones.

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rdf:type	Thing dul:ChemicalObject chemical substance Chemical compound yago:WikicatMonomers yago:Abstraction100002137 yago:Alcohol114708720 yago:Chemical114806838 yago:Compound114818238 yago:Diol114835980 yago:Fluid114939900 yago:Liquid114940386 yago:Material114580897 yago:Matter100020827 yago:Monomer114682963 yago:Part113809207 yago:PhysicalEntity100001930 yago:Relation100031921 chemical compound yago:Substance100019613 yago:WikicatDiols umbel-rc:ChemicalSubstanceType
rdfs:label	2,2,4,4-Tetramethyl-1,3-cyclobutandiol (de) 2,2,4,4-Tetramethyl-1,3-cyclobutanediol (en) 2,2,4,4-tetrametil-1,3-ciclobutanodiol (es) 2,2,4,4-tetramethyl-1,3-cyclobutaandiol (nl)
rdfs:comment	2,2,4,4-Tetramethyl-1,3-cyclobutanediol (CBDO) is an aliphatic diol. This diol is produced as a mixture of cis- and trans-isomers, depending on the relative stereochemistry of the hydroxyl groups. It is used as a monomer for the synthesis of polymeric materials. CBDO is currently being researched as an alternative to bisphenol A (BPA). BPA is a precursor used in the production of a wide range of polymers including polycarbonates, polyesters, polysulfones, and polyester ketones. (en) 2,2,4,4-Tetramethylcyclobutan-1,3-diol ist eine chemische Verbindung aus der Gruppe der Diole. Sie kommt in zwei isomeren Formen vor, der cis-Form und der trans-Form. (de) El 2,2,4,4-tetrametil-1,3-ciclobutanodiol es un diol alifático de fórmula molecular C8H16O2.Su estructura comprende un anillo de ciclobutano con dos grupos hidroxilo (-OH) en los extremos opuestos del mismo (posiciones 1 y 3). Unidos a cada una de las dos posiciones restantes (2 y 4) hay dos grupos metilo (-CH3).Los carbonos de las posiciones 1 y 3 del anillo son asimétricos, lo que convierte al 2,2,4,4-tetrametil-1,3-ciclobutanodiol en una molécula quiral con dos esteroisómeros, cis y trans. (es) 2,2,4,4-Tetramethyl-1,3-cyclobutaandiol (CBDO) is een alicyclisch diol. Er bestaat een trans- en een cis-stereo-isomeer van, met een verschillende ruimtelijke oriëntatie van de twee hydroxylgroepen. Het technisch product is een mengsel van de twee stereo-isomeren. (nl)
foaf:depiction
dcterms:subject	Diols Monomers Cyclobutanes
Wikipage page ID	22695288 (xsd:integer)
Wikipage revision ID	1118576650 (xsd:integer)
Link from a Wikipage to another Wikipage	Endocrine disruptor dbr:Bisphenol_A Rhodium Ruthenium Diols Monomers Ketene Ketone Polysulfone 2,2,4,4-Tetramethylcyclobutanedione Cis-trans isomerism Nickel Diol Isomer Cyclobutanes dbr:Isobutyric_acid Hydrogenation Polycarbonate Polymer Catalysts
Link from a Wikipage to an external page	http://fscimage.fishersci.com/msds/04302.htm
sameAs	2,2,4,4-Tetramethyl-1,3-cyclobutanediol 2,2,4,4-Tetramethyl-1,3-cyclobutanediol 2,2,4,4-Tetramethyl-1,3-cyclobutanediol 2,2,4,4-Tetramethyl-1,3-cyclobutanediol 2,2,4,4-Tetramethyl-1,3-cyclobutanediol 2,2,4,4-Tetramethyl-1,3-cyclobutanediol 2,2,4,4-Tetramethyl-1,3-cyclobutanediol 2,2,4,4-Tetramethyl-1,3-cyclobutanediol 2,2,4,4-Tetramethyl-1,3-cyclobutanediol 2,2,4,4-Tetramethyl-1,3-cyclobutanediol 2,2,4,4-Tetramethyl-1,3-cyclobutanediol
dbp:wikiPageUsesTemplate	dbt:Chembox dbt:Chembox_Hazards dbt:Chembox_Identifiers dbt:Chembox_Properties dbt:Reflist dbt:Cascite dbt:Chemspidercite dbt:Fdacite dbt:Stdinchicite
thumbnail	wiki-commons:Special:FilePath/CBDO.png?width=300
ImageAltL	Trans CBDO molecule (en)
ImageAltR	Cis CBDO molecule (en)
imagecaption	cis- and trans-2,2,4,4-Tetramethyl-1,3-cyclobutanediol (en)
ImageFile	CBDO.png (en)
ImageFileL	-CBDO-3D-balls.png (en)
ImageFileR	-CBDO-3D-balls.png (en)
ImageName	2244 (xsd:integer)
ImageSizeL	120 (xsd:integer)
ImageSizeR	120 (xsd:integer)
IUPACName	2244 (xsd:integer)
OtherNames	1133 (xsd:integer)
Verifiedfields	changed (en)
verifiedrevid	477209581 (xsd:integer)
Watchedfields	changed (en)
has abstract	2,2,4,4-Tetramethyl-1,3-cyclobutanediol (CBDO) is an aliphatic diol. This diol is produced as a mixture of cis- and trans-isomers, depending on the relative stereochemistry of the hydroxyl groups. It is used as a monomer for the synthesis of polymeric materials. CBDO is currently being researched as an alternative to bisphenol A (BPA). BPA is a precursor used in the production of a wide range of polymers including polycarbonates, polyesters, polysulfones, and polyester ketones. (en) 2,2,4,4-Tetramethylcyclobutan-1,3-diol ist eine chemische Verbindung aus der Gruppe der Diole. Sie kommt in zwei isomeren Formen vor, der cis-Form und der trans-Form. (de) El 2,2,4,4-tetrametil-1,3-ciclobutanodiol es un diol alifático de fórmula molecular C8H16O2.Su estructura comprende un anillo de ciclobutano con dos grupos hidroxilo (-OH) en los extremos opuestos del mismo (posiciones 1 y 3). Unidos a cada una de las dos posiciones restantes (2 y 4) hay dos grupos metilo (-CH3).Los carbonos de las posiciones 1 y 3 del anillo son asimétricos, lo que convierte al 2,2,4,4-tetrametil-1,3-ciclobutanodiol en una molécula quiral con dos esteroisómeros, cis y trans. (es) 2,2,4,4-Tetramethyl-1,3-cyclobutaandiol (CBDO) is een alicyclisch diol. Er bestaat een trans- en een cis-stereo-isomeer van, met een verschillende ruimtelijke oriëntatie van de twee hydroxylgroepen. Het technisch product is een mengsel van de twee stereo-isomeren. (nl)

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