Dodecanol

Dodecanol[1]
Identifiers
CAS number 112-53-8 YesY
PubChem 8193
ChemSpider 7901 YesY
UNII 178A96NLP2 YesY
DrugBank DB06894
KEGG C02277 YesY
ChEBI CHEBI:28878 YesY
ChEMBL CHEMBL24722 YesY
Jmol-3D images Image 1
Properties
Molecular formula C12H26O
Molar mass 186.34
Appearance Colorless solid
Density 0.8309
Melting point

24 °C, 297 K, 75 °F

Boiling point

259 °C, 532 K, 498 °F

Solubility in water 0.004 g/L[2]
Solubility in ethanol and diethyl ether Soluble
Hazards
R/S statement R36
Flash point 127 °C
 YesY (verify) (what is: YesY/N?)
Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa)
Infobox references

Dodecanol[pronunciation?], also known by its IUPAC name 1-dodecanol or dodecan-1-ol, and by its trivial name dodecyl alcohol and lauryl alcohol, is a fatty alcohol. Dodecanol is a colourless, water insoluble solid of melting point 24 °C and boiling point 259 °C. It has a floral aroma. It can be obtained from palm kernel or coconut oil fatty acids and methyl esters by reduction.

Dodecanol is used to make surfactants, lubricating oils, pharmaceuticals, in the formation of monolithic polymers and as a flavor enhancing food additive.

In cosmetics, dodecanol is used as an emollient.

Toxicity

Dodecanol is a mild skin irritant. It has about half the toxicity of ethanol, but it is very harmful to marine organisms.[3]

↑Jump back a section

Mutual solubility with water

The mutual solubility of 1-dodecanol and water has been quantified as follows.[4]

Mutual Solubility of Water and 1-Dodecanol (98%, Melting Point 24 °C), Weight %
Temperature, °C Solubility of Dodecanol in Water Solubility of Water in Dodecanol
29.5 0.04 2.87
40.0 0.05 2.85
50.2 0.09 2.69
60.5 0.15 2.96
70.5 0.09 2.70
80.3 0.14 2.89
90.8 0.18 2.96
standard deviation 0.02 0.01
↑Jump back a section

References

  1. ^ Merck Index, 12th Edition, 3464.
  2. ^ Record in the GESTIS Substance Database from the IFA
  3. ^ MSDS Safety Sheet
  4. ^ Richard Stephenson and James Stuart, "Mutual Binary Solubilities: Water-Alcohols and Water-Esters", J. Chem. Eng. Data, 1986, 31, 56-70.
↑Jump back a section

External links

↑Jump back a section

Read in another language

Last modified on 28 April 2013, at 00:30