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Chemical Structure| 111-20-6 Chemical Structure| 111-20-6
Chemical Structure| 111-20-6

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Decanedioic Acid is a naturally occurring dicarboxylic acid used in the synthesis. It is also a human metabolite and a plant metabolite.

Synonyms: Sebacic acid

4.5 *For Research Use Only !

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Product Citations

Product Citations

Keeler, Courtney Marie ;

Abstract: Polyhydroxyalkanoates are a class of biodegradable polyester, typically produced by fermentation, that could be a viable replacement to some petroleum-based plastics. This polymer is attractive to research because it is biodegradable, biocompatible, and does not form any microplastics which are harmful to both human health and the environment. PHAs show much promise, but have several factors to overcome including cost, availability, slow nucleation, poor mechanical properties, and aging which decreases PHAs flexibility over time. In this study, the latter two issues are focused on, as several biobased aliphatic polyesters are evaluated as additives to polyhydroxyalkanoates (PHAs) with the goal of increasing flexibility and preventing secondary crystallization. Poly(3-hydroxybutyrate-co-3-hydroxyhexanoate) with 6% and 8% hexanoate are the two PHAs utilized in this project. Blending and reactive extrusion of these PHAs and additives include polylactide, peroxide radical initiator, and novel aliphatic copolyesters synthesized by polycondensation is explored.

Keywords: Biodegradable ; polyhydroxyalkanoates ; polyesters ; extrusion ; polycondensation ; tensile testing

Purchased from AmBeed: ; ; ; ; ; ; ; 1071-76-7

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Product Details of Decanedioic acid

CAS No. :111-20-6
Formula : C10H18O4
M.W : 202.25
SMILES Code : O=C(O)CCCCCCCCC(O)=O
Synonyms :
Sebacic acid
MDL No. :MFCD00004440
InChI Key :CXMXRPHRNRROMY-UHFFFAOYSA-N
Pubchem ID :5192

Safety of Decanedioic acid

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Application In Synthesis of Decanedioic acid

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 111-20-6 ]

[ 111-20-6 ] Synthesis Path-Downstream   1~7

  • 4
  • [ 6066-82-6 ]
  • [ 111-20-6 ]
  • [ 159350-38-6 ]
  • 5
  • [ 111-20-6 ]
  • [ 4054-67-5 ]
  • 2C10H14N4*C10H18O4 [ No CAS ]
  • 6
  • [ 1004-38-2 ]
  • [ 111-20-6 ]
  • C4H7N5*2C10H18O4 [ No CAS ]
YieldReaction ConditionsOperation in experiment
67% In ethanol; water; for 0.5h; General procedure: To a 10 ml of ethanol-H2O mixed solution containing H2NPA(0.20 mmol) and <strong>[1004-38-2]TAP</strong>I (0.10 mmol) was stirred for half an hourcontinually. The resulting clear solution was evaporated at20e25 C, and an irregular, colorless bulk crystal was obtained afterseven days. The resulting crystals were filtered and dried afterrinsed with ethanol-H2O mixed solution. Yield: 70%. Analysiscalculated for C12H14N6O7: C, 40.64; H, 3.95; N, 23.71%. Found: C,40.35; H, 4.00; N, 23.51%. Infrared spectrum (KBr disc, cm1):3441s, 3409s, 3208m, 3082m, 2416w, 1679s, 1651s, 1607s, 1569s,1538s, 1454m, 1431m, 1413m, 1351s, 1261m, 1155m, 1133w, 1077w,972w, 912m, 843w, 830m, 810m, 782s, 763m, 705s, 661w, 587m,532s.
  • 7
  • [ 82410-79-5 ]
  • [ 111-20-6 ]
  • cadmium(II) nitrate tetrhydrate [ No CAS ]
  • C10H16O4(2-)*Cd(2+)*C16H18N4 [ No CAS ]
YieldReaction ConditionsOperation in experiment
65% General procedure: A mixture of sebacic acid (0.101 g, 0.5 mmol), Cd(NO3)2·4H2O(0.154 g, 0.5 mmol), 1,2-mbix (0.134 g, 0.5 mmol) and water (10 mL)was stirred for 30 min. The pH value of the mixture was adjusted to 6.0with 1 mol L-1 NaOH solution, and then the resulting mixture wastransferred and sealed in a 25 mL Teflon-lined stainless-steel containerand heated at 160 C for three days. After slowly cooled to room temperature, the brown crystals of 1 were collected.
 

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