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Merck

124672

Sigma-Aldrich

10-Undecenoic acid

98%

Sinónimos:

Undecylenic acid

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About This Item

Fórmula lineal:
CH2=CH(CH2)8COOH
Número de CAS:
Peso molecular:
184.28
Colour Index Number:
42650
Beilstein/REAXYS Number:
1762631
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

assay

98%

form

solid

refractive index

n20/D 1.449 (lit.)

bp

137 °C/2 mmHg (lit.)

mp

23-25 °C (lit.)

solubility

H2O: insoluble
alcohol: soluble
chloroform: soluble
diethyl ether: soluble

density

0.912 g/mL at 25 °C (lit.)

functional group

allyl
carboxylic acid

SMILES string

OC(=O)CCCCCCCCC=C

InChI

1S/C11H20O2/c1-2-3-4-5-6-7-8-9-10-11(12)13/h2H,1,3-10H2,(H,12,13)

InChI key

FRPZMMHWLSIFAZ-UHFFFAOYSA-N

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General description

10-Undecenoic acid undergoes copolymerisation with ethylene using the metallocene catalyst system Cp2ZrCl2 / methylaluminoxane.

Application

10-Undecenoic acid has been used to study the methods and mechanisms for the formation of molecular monolayers on silicon surface. It was used as starting reagent in the syntheses of pheromone (11Z)-hexadecenal and agriculturally important insect pheromones.

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Aquatic Chronic 3 - Eye Irrit. 2 - Skin Irrit. 2

Storage Class

11 - Combustible Solids

wgk_germany

WGK 1

flash_point_f

300.2 °F - closed cup

flash_point_c

149 °C - closed cup

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves


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10-Undecenoic acid, an inexpensive source for the synthesis of the pheromones of cotton pests, peach tree borer and cherry tree borer.
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Molecules (Basel), 2(6), 87-90 (1997)
Metallocene-Catalysed Copolymerisation of Ethylene with 10-Undecenoic Acid: The Effect of Experimental Conditions.
Santos JM, et al.
Macromolecular Chemistry and Physics, 202(11), 2195-2201 (2001)
Molecular monolayers on silicon surfaces.
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