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T1894

Sigma-Aldrich

cis-9-Tetradecenol

~95%

Synonym(s):

(Z)-9-TDOL, Myristoleyl alcohol, Z-9-TDOL

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About This Item

Linear Formula:
CH3(CH2)3CH=CH(CH2)8OH
CAS Number:
35153-15-2
Molecular Weight:
212.37
EC Number:
252-401-7
MDL number:
MFCD00009993
UNSPSC Code:
12352200
PubChem Substance ID:
24899995

assay

~95%

refractive index

n20/D 1.457 (lit.)

storage temp.

−20°C

SMILES string

[H]\C(CCCC)=C(/[H])CCCCCCCCO

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Biochem/physiol Actions

Pheromone for Homoeosoma electellum

Packaging

Sealed ampule (liquid).

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Storage Class

10 - Combustible liquids

wgk_germany

WGK 3

flash_point_f

143.6 °F - closed cup

flash_point_c

62 °C - closed cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

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Certificates of Analysis (COA)

Lot/Batch Number
030K15641
023F01142

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T J O'Leary et al.
Biophysical journal, 50(6), 1053-1059 (1986-12-01)
The effects of cis- and trans-9,10-tetradecenols on the phase transitions of dimyristoyl-, dipalmitoyl-, and distearoyl-phosphatidylcholines were investigated using high sensitivity scanning calorimetry and Raman spectroscopy. Both alcohols lowered the gel to liquid crystalline phase transition temperatures for all three phosphatidylcholines
S B Jiang et al.
Journal of immunological methods, 126(1), 29-37 (1990-01-24)
Perforin-mediated lysis consists of at least three steps: perforin binding to the target cell, insertion into the plasma membrane, and polymerization to form pores. Perforin binding, the first step, is critical for pore formation. Accordingly, a competition assay was here
M M Ndengele et al.
Experimental parasitology, 81(2), 191-201 (1995-09-01)
We studied the effects of membrane modulation on the interaction of Plasmodium falciparum rhoptry proteins of 140/130/110 kDa (Rhop-H) with human and mouse erythrocytes. Cells treated with 2-(2-methoxyethoxy)ethyl-8-(cis-2-n-octylcyclopropyl)octanoate, myristoleyl alcohol, and proteins extracted with sublytic concentrations of membrane solubilizing detergents
Julio C Rojas et al.
Journal of economic entomology, 99(3), 797-802 (2006-07-04)
Chemical and electrophysiological analyses and field trials were used to identify the female sex pheromone of Copitarsia decolora (Guenée) (Lepidoptera: Noctuidae). Coupled gas chromatographic-electroantennographic detection (GC-EAD) analysis of the female gland extract showed the presence of two EAD-active peaks, which
D Morse et al.
The Journal of biological chemistry, 259(1), 475-480 (1984-01-10)
Highly sensitive, luminescent assays have been developed to measure enzyme activities involved in the metabolism of a major class of insect pheromones which includes fatty aldehydes, alcohols, and their acetate esters. These assays have been applied to measure the in
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