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27519-02-4

  • Product Name:cis-9-Tricosene
  • Molecular Formula:C23H46
  • Molecular Weight:322.618
  • Appearance:clear colourless to slightly yellow liquid
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Product Details

pd_meltingpoint:0°C

Appearance:clear colourless to slightly yellow liquid

Purity:99%

Factory Supply Industrial Grade cis-9-Tricosene 27519-02-4 with Best Price

  • Molecular Formula:C23H46
  • Molecular Weight:322.618
  • Appearance/Colour:clear colourless to slightly yellow liquid 
  • Vapor Pressure:3.16E-06mmHg at 25°C 
  • Melting Point:0°C 
  • Refractive Index:n20/D 1.453(lit.)  
  • Boiling Point:399.4 °C at 760 mmHg 
  • Flash Point:208.9 °C 
  • PSA：0.00000 
  • Density:0.802 g/cm3 
  • LogP:8.99430 

cis-9-Tricosene(Cas 27519-02-4) Usage

Safety Profile

Moderately toxic by skin contact.When heated to decomposition it emits acrid smoke andirritating vapors.

Metabolic pathway

Muscalure is a long chain mono-unsaturated hydrocarbon and the 9,lO-double bond is a reactive site towards biologrcal and non-biological oxidative agents.

Degradation

Muscalure is stable to light and temperatures up to 50 °C for one year.

General Description

Muscalure is an insect pheromone utilized to attract houseflies. It is generally used as a coactive ingredient in fly-bait products.

InChI:InChI=1/C23H46/c1-3-5-7-9-11-13-15-17-19-21-23-22-20-18-16-14-12-10-8-6-4-2/h17,19H,3-16,18,20-23H2,1-2H3/b19-17+

27519-02-4 Relevant articles

The synthesis of long chain dialkylalkynes, dialkyldiynes and their hydrogenation to monoenes and dienes

Fisher,Tyman

, p. 1323 - 1338 (1998)

Long methylenic chain dialkylalkynes hav...

INSECT PHEROMONES AND THEIR ANALOGS. XIV. SYNTHESIS OF MUSCALURE - THE SEX PHEROMONE OF Musca domestica

Odinokov, V. N.,Ishmuratov, G. Yu.,Balezina, G. G.,Bakhitov, R. Sh.,Tolstikov, G. A.

, p. 375 - 377 (1985)

A new route to the synthesis of tricos-9...

A stereospecific route to functionalized alkenes from tetrahydrofurfurylic acetates, synthesis of pheromones

Amouroux, Roger,Ejjiyar, Soumeya

, p. 3059 - 3062 (1991)

Pure Z or E γ-iodoalkenes were prepared ...

REGIOSELECTION IN THE ALKYLATION OF TRIMETHYLSILYLALLYL ANION- STEREOSELECTIVE SYNTHESIS OF DISUBSTITUTED ALKENES.

Koumaglo, K.,Chan, T. H.

, p. 717 - 720 (1984)

The regioselection in the alkylation of ...

New simple synthesis of the housefly sex attractant

Yen, Yao-Pin,Wang, Fey-Long

, p. 494 - 496 (1997)

-

Synthesis of the housefly sex attractant.

Cargill,Rosenblum

, p. 3971 - 3971 (1972)

-

Electrochemical synthesis of the sex attractant pheromone of the housefly: (Z)-9-tricosene

Yadav,Tissot

, p. 1698 - 1701 (1984)

-

A NEW STEREOSELECTIVE SYNTHESIS OF (Z)-9-TRICOSENE, THE SEX ATTRACTANT OF THE COMMON HOUSEFLY

Moiseenkov, Alexander M.,Schaub, Bruno,Margot, Christian,Schlosser, Manfred

, p. 305 - 306 (1985)

"Muscalure" (9-tricosene) was prepared v...

Synthesis of tricosen-(9-cis), Muscalure, a housefly attractant

Eiter,Joop

, p. 468 - 469 (1972)

-

A synthesis of muscalure, the housefly sex attractant

Ho,Wong

, p. 1923 - 1924 (1974)

-

Cobalt-Catalyzed Decarboxylative Methylation and Ethylation of Aliphatic N-(Acyloxy)phthalimides with Organoaluminum Reagents

Wang, Ze-Zhong,Wang, Guang-Zu,Zhao, Bin,Shang, Rui,Fu, Yao

supporting information, p. 1221 - 1225 (2020/08/17)

A cobalt-catalyzed decarboxylative methy...

Stereoselective Alkyne Hydrogenation by using a Simple Iron Catalyst

Gregori, Bernhard J.,Schwarzhuber, Felix,P?llath, Simon,Zweck, Josef,Fritsch, Lorena,Schoch, Roland,Bauer, Matthias,Jacobi von Wangelin, Axel

, p. 3864 - 3870 (2019/07/31)

The stereoselective hydrogenation of alk...

Practical and scalable synthesis of (Z)-9-Tricosene, the housefly sex pheromone

Kim, Miri,Pitchaiah, Arigala,Park, No-Joong,Hwang, In Taek,Lee, Kee-In

, p. 628 - 631 (2013/02/23)

A practical and scalable synthesis of (Z...

Stereoselective cometathesis of 1,5-cyclooctadiene with ethylene as an efficient pathway to Z-ene biologically active natural products

Bykov,Goletiani,Butenko,Finkel'shtein

, p. 163 - 166 (2007/10/03)

-

27519-02-4 Process route

9-Diphenylphosphinoyltricosan-10-ol

9-Diphenylphosphinoyltricosan-10-ol

(Z)-tricos-9-ene
27519-02-4

(Z)-tricos-9-ene

trans-9-tricosene
35857-62-6

trans-9-tricosene

Conditions
Conditions Yield
With potassium hydride; In N,N-dimethyl-formamide; at 50 ℃; for 0.5h; Yield given. Yields of byproduct given. Title compound not separated from byproducts;
nonan-1-al
124-19-6

nonan-1-al

(n-tetradecyl)triphenylphosphonium bromide
25791-20-2

(n-tetradecyl)triphenylphosphonium bromide

(Z)-tricos-9-ene
27519-02-4

(Z)-tricos-9-ene

trans-9-tricosene
35857-62-6

trans-9-tricosene

Conditions
Conditions Yield
(n-tetradecyl)triphenylphosphonium bromide; With n-butyllithium; In tetrahydrofuran; dimethyl sulfoxide; at 10 - 15 ℃; for 0.0833333h;
nonan-1-al; In tetrahydrofuran; dimethyl sulfoxide; at 20 ℃; for 0.5h;

27519-02-4 Upstream products

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    39487-08-6

    tricos-9-yne

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    1-decyne

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    2437-56-1

    1-tridecene

  • 124-19-6
    124-19-6

    nonan-1-al

27519-02-4 Downstream products

  • 124-19-6
    124-19-6

    nonan-1-al

  • 124-25-4
    124-25-4

    myristylaldehyde

  • 35857-62-6
    35857-62-6

    trans-9-tricosene

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