Dodecanedioic acid explained

Dodecanedioic acid (DDDA) is a dicarboxylic acid with the formula . A white solid, the compound finds a variety of applications ranging from polymers to materials. The unbranched compound is the most commonly encountered C12 dicarboxylic acid.

Production

DDDA has traditionally been produced from butadiene using a multi-step chemical process.[1] Butadiene is first converted to cyclododecatriene through cyclotrimerization.[2] The triene is then hydrogenated to cyclododecane. Autoxidation by air in the presence of boric acid gives a mixture of cyclodecanol and the cyclododecanone. In the final step, this mixture oxidized to the diacid using nitric acid. An alternative route involves ozonolysis of cyclododecene.[3]

Biological process

Paraffin wax can be converted into DDDA on a laboratory scale[4] with a special strain of Candida tropicalis yeast in a multi-step process.[5] Renewable plant-oil feedstocks sourced from switchgrass could also be used to produce DDDA.

Uses

DDDA is used in antiseptics, top-grade coatings, painting materials, corrosion inhibitors, surfactants, and polymers. It is one of two precursors to the engineering plastic nylon 612.[6] The once commercial nylon called Qiana was produced on scale using DDDA.

Medical

In type 2 diabetic patients DDDA demonstrated that IV infusion helps to maintain normal blood sugar and energy levels without increasing the blood glucose load in the process.[7]

References

  1. Web site: BIOLON® DDDA. verdezyne.com. 2016-09-23. https://web.archive.org/web/20160924105309/http://verdezyne.com/products/dodecanedioic-acid-ddda/. 2016-09-24. dead.
  2. Book: Klaus Weissermel, Hans-Jurgen Arpe . Industrial Organic Chemistry . John Wiley & Sons . 3rd . 1997 . 3-527-28838-4.
  3. Book: 10.1002/14356007.a08_523.pub3. Dicarboxylic Acids, Aliphatic . Ullmann's Encyclopedia of Industrial Chemistry . 2014 . Cornils . Boy . Lappe . Peter . By Staff . Updated . 1–18 . 9783527306732 .
  4. Web site: Dibasic acids. www.cathaybiotech.com. 2019-03-15. 2018-10-09. https://web.archive.org/web/20181009225209/http://www.cathaybiotech.com/en/product.aspx. dead.
  5. Kroha . Kyle . Industrial biotechnology provides opportunities for commercial production of new long-chain dibasic acids . Inform . 15(9) . Sep 2004 . 568 . 15 March 2019 . American Oil Chemists Society . https://web.archive.org/web/20141006184727/http://aocs.files.cms-plus.com/inform/2004/9/dibasicacids.pdf . 6 October 2014 . dead .
  6. [Nylon#Homopolymers]
  7. 9591306. 1998. Greco. A. V.. The metabolic effect of dodecanedioic acid infusion in non-insulin-dependent diabetic patients. Nutrition. 14. 4. 351–7. Mingrone. G. Capristo. E. Benedetti. G. De Gaetano. A. Gasbarrini. G . 10.1016/s0899-9007(97)00502-9.