Dibutyl adipate
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| General | ||||||||||||||||
| Surname | Dibutyl adipate | |||||||||||||||
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| Molecular formula | C 14 H 26 O 4 | |||||||||||||||
| Brief description |
colorless liquid with a faint odor |
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| properties | ||||||||||||||||
| Molar mass | 258.36 g mol −1 | |||||||||||||||
| Physical state |
liquid |
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| density |
0.961 g cm −3 |
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| Melting point |
−38 ° C |
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| boiling point |
305 ° C |
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| Vapor pressure |
<0.1 Pa (20 ° C) |
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| solubility |
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| Refractive index |
1.4369 (at 20 ° C) |
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| safety instructions | ||||||||||||||||
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| As far as possible and customary, SI units are used. Unless otherwise noted, the data given apply to standard conditions . Refractive index: Na-D line , 20 ° C | ||||||||||||||||
Adipic acid dibutyl ester is a chemical compound from the group of carboxylic acid esters .
Extraction and presentation
Dibutyl adipate can be obtained by esterification of adipic acid with butyl alcohol or by transesterification of diethyl adipate .
properties
Adipic acid dibutyl ester is a flammable, hardly inflammable, colorless liquid ( flash point > 113 ° C) with a weak odor, which is practically insoluble in water.
use
Dibutyl adipate is used in cosmetics as a skin care product and film former. In PVC it serves as a plasticizer .
Individual evidence
- ↑ Entry on DIBUTYL ADIPATE in the CosIng database of the EU Commission, accessed on December 29, 2019.
- ↑ a b c d e f g h i j k l m Entry on dibutyl adipate in the GESTIS substance database of the IFA , accessed on September 8, 2019(JavaScript required) .
- ↑ a b David R. Lide: CRC Handbook of Chemistry and Physics A Ready-reference Book of Chemical and Physical Data . CRC Press, 1995, ISBN 978-0-8493-0595-5 , pp. 160 ( limited preview in Google Book Search).
- ↑ Google Patents: CN104058964A - Preparation method for dibutyl adipate - Google Patents , accessed September 8, 2019.
- ^ Stefan Koenig: Scalable Green Chemistry Case Studies from the Pharmaceutical Industry . CRC Press, 2013, ISBN 978-981-4364-81-2 , pp. 315 ( limited preview in Google Book search).
- ↑ Marina Bährle-Rapp: Springer Lexicon Cosmetics and Body Care . Springer-Verlag, 2013, ISBN 978-3-662-09983-4 , pp. 124 ( limited preview in Google Book search).
- ^ Helmuth Kainer: Polyvinyl chloride and vinyl chloride copolymers chemistry and chemical technology . Springer-Verlag, 2013, ISBN 978-3-642-87892-3 , pp. 263 ( limited preview in Google Book search).
- ↑ unknown: Amended Final Report of the Safety Assessment of Dibutyl Adipate as Used in Cosmetics1. In: International Journal of Toxicology. 25, 2016, p. 129, doi : 10.1080 / 10915810600716679 .