1,10-decanediol

Structural formula
General
Surname	1,10-decanediol
other names	Decamethylene glycol
Molecular formula	C 10 H 22 O 2
Brief description	white solid
External identifiers / databases
EC number	203-975-2
ECHA InfoCard	100.003.614
PubChem	37153
Wikidata	Q20054514
properties
Molar mass	174.28 g mol −1
Physical state	firmly
density	0.891 g cm −3 (80 ° C)
Melting point	72-75 ° C
boiling point	297 ° C (1,013 hPa); 170 ° C (11 hPa);
Vapor pressure	<0.1 hPa (20 ° C)
solubility	poorly soluble in water
safety instructions
GHS labeling of hazardous substances	no GHS pictograms
	no GHS pictograms
H and P phrases	H: no H-phrases
	P: no P-phrases
	As far as possible and customary, SI units are used. Unless otherwise noted, the data given apply to standard conditions .

1,10-decanediol is an organic chemical compound from the group of alkanediols .

properties

1,10-decanediol is a white solid that is poorly soluble in water. The molecule has a zigzag structure.

use

1,10-decanediol can be used to produce other chemical compounds such as the musk fragrance (E) -1,6-dioxacyclohexadec-3-ene. 1,10-dibromodecane can be obtained by bromination . 1,10-dichlorodecane can be obtained by reaction with thionyl chloride .

Individual evidence

↑ ^a ^b ^c ^d ^e ^f ^g ^h ⁱ ^j data sheet 1,10-decanediol, 98% from Sigma-Aldrich , accessed on April 30, 2015 ( PDF ).
↑ ^a ^b William M. Haynes: CRC Handbook of Chemistry and Physics, 95th Edition: . CRC Press, 2014, ISBN 978-1-4822-0868-9 , pp. 142 ( limited preview in Google Book search).
↑ N. Nakamura, T. Sato: 1,10-decanediol. In: Acta Crystallographica Section C Crystal Structure Communications. 55, 1999, pp. 1685-1687, doi: 10.1107 / S0108270199008318 .
↑ Eberhard Breitmaier, Günther Jung: Organic Chemistry, 7th complete revision. u. exp. Edition 2012: Basics, compound classes, reactions, concepts, molecular structure, natural substances, synthesis planning, sustainability . Georg Thieme Verlag, 2014, ISBN 978-3-13-159987-2 , p. 635 ( limited preview in Google Book search).
↑ Rong Lu, Tetsuo Miyakoshi: Lacquer Chemistry and Applications . Elsevier, 2015, ISBN 978-0-12-803610-5 , pp. 157 ( limited preview in Google Book search).
^ Scientific Papers of the Institute of Physical and Chemical Research . The Institute, 1931, p. 12 ( limited preview in Google Book search).

[Sigma-1] ↑ ^a ^b ^c ^d ^e ^f ^g ^h ⁱ ^j data sheet 1,10-decanediol, 98% from Sigma-Aldrich , accessed on April 30, 2015 ( PDF ).

[William_M._Haynes-2] William M. Haynes: CRC Handbook of Chemistry and Physics, 95th Edition: . CRC Press, 2014, ISBN 978-1-4822-0868-9 , pp. 142 ( limited preview in Google Book search).

[DOI10.1107/S0108270199008318-3] N. Nakamura, T. Sato: 1,10-decanediol. In: Acta Crystallographica Section C Crystal Structure Communications. 55, 1999, pp. 1685-1687, doi: 10.1107 / S0108270199008318 .

[Eberhard_Breitmaier,_Günther_Jung-4] Eberhard Breitmaier, Günther Jung: Organic Chemistry, 7th complete revision. u. exp. Edition 2012: Basics, compound classes, reactions, concepts, molecular structure, natural substances, synthesis planning, sustainability . Georg Thieme Verlag, 2014, ISBN 978-3-13-159987-2 , p. 635 ( limited preview in Google Book search).

[Rong_Lu,_Tetsuo_Miyakoshi-5] Rong Lu, Tetsuo Miyakoshi: Lacquer Chemistry and Applications . Elsevier, 2015, ISBN 978-0-12-803610-5 , pp. 157 ( limited preview in Google Book search).

[6] Scientific Papers of the Institute of Physical and Chemical Research . The Institute, 1931, p. 12 ( limited preview in Google Book search).