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1-Tridecanol

From Wikipedia, the free encyclopedia
1-Tridecanol
Names
Preferred IUPAC name
Tridecan-1-ol
Other names
1-Tridecanol
Tridecyl alcohol
Identifiers
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
ECHA InfoCard100.003.635Edit this at Wikidata
UNII
  • InChI=1S/C13H28O/c1-2-3-4-5-6-7-8-9-10-11-12-13/h13H,2-13H2,1H3 ☒N
    Key: needed ☒N
  • InChI=1/C13H28O/c1-2-3-4-5-6-7-8-9-10-11-12-13/h13H,2-13H2,1H3
    Key: needed
  • CCCCCCCCCCCCCO
Properties
C13H28O
Molar mass200.366 g·mol−1
AppearanceWhite solid[1]
Density0.84 g/cm3[1]
Melting point32 °C (90 °F; 305 K)[1]
Boiling point274–280 °C (525–536 °F; 547–553 K)[1]
Practically insoluble in water[1]
Hazards
GHS labelling:
GHS07: Exclamation mark
H315,H319,H335
P261,P264,P271,P280,P302+P352,P304+P340+P312,P305+P351+P338,P332+P313,P337+P313,P362,P403+P233,P405,P501
NFPA 704 (fire diamond)
Flash point120 °C
260 °C
Lethal dose or concentration (LD, LC):
17200 mg/kg (rat, oral)[1]
Except where otherwise noted, data are given for materials in theirstandard state (at 25 °C [77 °F], 100 kPa).
Chemical compound

1-Tridecanol (Tridecanol) is anorganic compound with the formulaCH3(CH2)11CH2OH. It is a colorless oily solid that is classified as a primaryalcohol.

Like related long chain alcohols, tridecanol is sometimes classified as afatty alcohol because they were once obtained by hydrogenation of fats.[2] Most fatty alcohols, however, have even numbers of carbons. 1-Tridecanol can be obtained by hydrogenation oftridecanal. 1-Tridecanol is used as alubricant and for the manufacture ofsurfactants andplasticizers.

References

[edit]
  1. ^abcdefRecord in theGESTIS Substance Database of theInstitute for Occupational Safety and Health
  2. ^Falbe, Jürgen; Bahrmann, Helmut; Lipps, Wolfgang; Mayer, Dieter; Frey, Guido D. (2013). "Alcohols, Aliphatic".Ullmann's Encyclopedia of Industrial Chemistry.doi:10.1002/14356007.a01_279.pub2.ISBN 978-3-527-30385-4.
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