1-pentadecanol

Structural formula
General
Surname	1-pentadecanol
other names	Pentadecyl alcohol; Pentadecan-1-ol;
Molecular formula	C 15 H 32 O
Brief description	white solid
External identifiers / databases
EC number	211-107-9
ECHA InfoCard	100.010.099
PubChem	12397
Wikidata	Q27146999
properties
Molar mass	228.41 g mol −1
Physical state	firmly
Melting point	41-44 ° C
boiling point	269-271 ° C
solubility	practically insoluble 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-Pentadecanol is a chemical compound from the group of linear alkanols .

Occurrence

1-Pentadecanol occurs naturally in Hymenoptera .

Extraction and presentation

1-Pentadecanol can be obtained by reacting silver palmitate with iodine .

The synthesis is also possible by reacting hexadecene at low temperature with ozone to form the corresponding ozonide , which is reduced to 1-pentadecanol with sodium borohydride .

properties

1-Pentadecanol is a white fluffy solid that is practically insoluble in water.

use

1-Pentadecanol is used as a starting material for the production of other chemical compounds (e.g. Jaspin B).

Individual evidence

↑ ^a ^b ^c ^d ^e ^f ^g data sheet 1-pentadecanol, 99% from Sigma-Aldrich , accessed on August 17, 2018 ( PDF ).
↑ ^a ^b Data sheet 1-Pentadecanol, 99% from AlfaAesar, accessed on August 17, 2018 ( PDF )(JavaScript required) .
↑ E. David Morgan, N. Bhushan Mandava: Handbook of Natural Pesticides Pheromono . CRC Press, 1988, ISBN 978-0-8493-3658-4 , pp. 146 ( limited preview in Google Book search).
^ Frank C. Whitmore: Organic Chemistry, Volume One Part I: Aliphatic Compounds Part II: Alicyclic Compounds . Courier Corporation, 2012, ISBN 978-0-486-60700-9 , pp. 132 ( limited preview in Google Book search).
↑ Practical Preparation of Pentadecanol and 1 Bromopentadecane from 1 Hexadecene - 《CHINESE JOURNAL OF PHARMACEUTICALS》 2000 年 05 期: Practical Preparation of Pentadecanol and 1 Bromopentadecane from 1 Hexadecene - 《CHINESE JOURNAL OF PHARMACEUTICALS accessed on May 17, 2000 August 2018.

↑ K. Venkatesan, KV Srinivasan: A novel stereoselective synthesis of pachastrissamine (jaspine B) starting from 1-pentadecanol. In: Tetrahedron: Asymmetry. 19, 2008, p. 209, doi : 10.1016 / j.tetasy.2007.12.001 .

[Sigma-1] ↑ ^a ^b ^c ^d ^e ^f ^g data sheet 1-pentadecanol, 99% from Sigma-Aldrich , accessed on August 17, 2018 ( PDF ).

[Alfa-2] Data sheet 1-Pentadecanol, 99% from AlfaAesar, accessed on August 17, 2018 ( PDF )(JavaScript required) .

[E._David_Morgan,_N._Bhushan_Mandava-3] E. David Morgan, N. Bhushan Mandava: Handbook of Natural Pesticides Pheromono . CRC Press, 1988, ISBN 978-0-8493-3658-4 , pp. 146 ( limited preview in Google Book search).

[Frank_C._Whitmore-4] Frank C. Whitmore: Organic Chemistry, Volume One Part I: Aliphatic Compounds Part II: Alicyclic Compounds . Courier Corporation, 2012, ISBN 978-0-486-60700-9 , pp. 132 ( limited preview in Google Book search).

[cnki.com.cn-5] Practical Preparation of Pentadecanol and 1 Bromopentadecane from 1 Hexadecene - 《CHINESE JOURNAL OF PHARMACEUTICALS》 2000 年 05 期: Practical Preparation of Pentadecanol and 1 Bromopentadecane from 1 Hexadecene - 《CHINESE JOURNAL OF PHARMACEUTICALS accessed on May 17, 2000 August 2018.

[DOI10.1016/j.tetasy.2007.12.001-6] K. Venkatesan, KV Srinivasan: A novel stereoselective synthesis of pachastrissamine (jaspine B) starting from 1-pentadecanol. In: Tetrahedron: Asymmetry. 19, 2008, p. 209, doi : 10.1016 / j.tetasy.2007.12.001 .