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Glutaric acid may cause irritation to the skin and eyes. Acute hazards include the fact that this compound may be harmful by ingestion, inhalation or skin absorption.
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Peter Werle and Marcus
Morawietz "Alcohols, Polyhydric" in Ullmann's Encyclopedia of Industrial Chemistry: 2002, Wiley-VCH: Weinheim. DOI 10.1002/14356007.a01_305
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are water-soluble only to a few percent at room temperature, the water-solubility of glutaric acid is over 50% (w/w).
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791:, Shipchandler, Mohammed T., "Method of synthesis of pyrogallol", published 1977-09-06, assigned to
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G. Paris, L. Berlinguet, R. Gaudry, J. English, Jr. and J. E. Dayan (1957). "Glutaric Acid and
Glutaramide".
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655:. The odd number of carbon atoms (i.e. 5) is useful in decreasing polymer elasticity.
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that is hydrolyzed to the diacid. Alternatively hydrolysis, followed by oxidation of
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Glutaric acid itself has been used in the production of polymers such as polyester
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Except where otherwise noted, data are given for materials in their
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Calculator: Water and solute activities in aqueous glutaric acid
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Advanced
Organic Chemistry: Reactions, Mechanisms, and Structure
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735:(6th ed.), New York: Wiley-Interscience, p. 1736,
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gives glutaric acid. It can also be prepared from reacting
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Glutaric acid is naturally produced in the body during the
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95 to 98 °C (203 to 208 °F; 368 to 371 K)
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to obtain the dinitrile, followed by hydrolysis. Using
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in this metabolic pathway can lead to a disorder called
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InChI=1S/C5H8O4/c6-4(7)2-1-3-5(8)9/h1-3H2,(H,6,7)(H,8,9)
572:, where toxic byproducts build up and can cause severe
482:
371:
InChI=1/C5H8O4/c6-4(7)2-1-3-5(8)9/h1-3H2,(H,6,7)(H,8,9)
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Glutaric acid can be prepared by the ring-opening of
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458:200 °C (392 °F; 473 K) /20 mmHg
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592:to give the potassium salt of the carboxylate-
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8:
709:: CS1 maint: multiple names: authors list (
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765:"Glutaric acid, Pentanedioic acid, 99%"
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620:, which proceeds with decarboxylation.
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661:can be produced from glutaric diester.
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644:of glutaric acid and its derivatives.
364:Key: JFCQEDHGNNZCLN-UHFFFAOYSA-N
161:
141:
7:
864:Linear saturated dicarboxylic acids
616:, it is obtained from oxidation of
374:Key: JFCQEDHGNNZCLN-UHFFFAOYAU
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14:
529:. Although the related "linear"
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38:
29:
468:(at 25 °C , 100 kPa).
1:
68:Propane-1,3-dicarboxylic acid
70:1,3-Propanedicarboxylic acid
1106:Category:Dicarboxylic acids
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438:132.12 g/mol
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1103:
1065:Hexadecanedioic acid
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28:
1084:(Phelogenic acid) C
1048:Tredecanedioic acid
698:10.15227/orgsyn.037.0047
16:Not to be confused with
1031:Dodecanedioic acid
963:Heptanedioic acid
929:(Glutaric acid) C
927:Pentanedioic acid
911:(Succinic acid) C
897:(Malonic acid) CH
895:Propanedioic acid
887:(Oxalic acid) (CO
1067:(Thapsic acid) C
1016:(Sebacic acid) C
1014:Decanedioic acid
999:(Azelaic acid) C
997:Nonanedioic acid
982:(Suberic acid) C
980:Octanedioic acid
965:(Pimelic acid) C
945:Hexanedioic acid
909:Butanedioic acid
885:Ethanedioic acid
76:1,5-Pentanedioic acid
947:(Adipic acid) C
815:, cameochemicals.com
618:1,3-cyclohexanedione
53:Preferred IUPAC name
725:Smith, Michael B.;
640:is manufactured by
74:n-Pyrotartaric acid
25:
1125:Dicarboxylic acids
1082:Docosanedioic acid
1050:(Brassylic acid) C
793:IMC Chemical Group
602:1,3-dibromopropane
531:dicarboxylic acids
495:Infobox references
23:
1112:
1111:
742:978-0-471-72091-1
689:Organic Syntheses
636:and precursor to
610:potassium cyanide
590:potassium cyanide
570:glutaric aciduria
503:Chemical compound
501:
500:
395:C(CC(=O)O)CC(=O)O
317:CompTox Dashboard
123:Interactive image
72:Pentanedioic acid
57:Pentanedioic acid
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18:Glutamic acid
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772:. Retrieved
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727:March, Jerry
720:
705:cite journal
687:
681:
669:
598:dihydropyran
583:
556:, including
547:
544:Biochemistry
506:
505:
82:Identifiers
64:Other names
769:Chemkits.eu
634:plasticizer
632:, a common
554:amino acids
404:Properties
221:100.003.471
143:CHEBI:17859
789:US 4046817
774:2020-09-29
674:References
659:Pyrogallol
653:polyamides
638:polyesters
580:Production
562:tryptophan
550:metabolism
434:Molar mass
305:H849F7N00B
174:ChemSpider
110:3D model (
89:CAS Number
614:periodate
513:with the
242:203-817-2
234:EC Number
1119:Category
729:(2007),
552:of some
194:DrugBank
99:110-94-1
649:polyols
594:nitrile
566:Defects
515:formula
509:is the
488:what is
486: (
428:
272:PubChem
203:DB03553
870:C-R-CO
798:
739:
692:: 47.
666:Safety
606:sodium
558:lysine
534:adipic
525:(COOH)
483:verify
480:
388:SMILES
260:C00489
154:ChEMBL
47:Names
604:with
588:with
353:InChI
134:ChEBI
112:JSmol
737:ISBN
711:link
624:Uses
560:and
536:and
296:UNII
251:KEGG
955:(CO
937:(CO
919:(CO
901:(CO
866:(HO
694:doi
608:or
322:EPA
285:743
275:CID
183:723
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