50933-33-0 Usage
Uses
Used in Pest Management:
GOSSYPLURE is used as a sex attractant for cotton bollworms and pink bollworms, two major pests of cotton crops. By mimicking the natural pheromones released by female moths, it lures male moths into traps, thereby disrupting their mating patterns and reducing their population. This helps in controlling the damage caused by these pests to cotton crops and reduces the need for chemical pesticides.
Used in Agriculture:
In the agricultural industry, GOSSYPLURE is used as a biopesticide to protect cotton crops from the damage caused by cotton bollworms and pink bollworms. By employing this pheromone-based approach, farmers can effectively manage these pests without resorting to harmful chemical pesticides, promoting sustainable and eco-friendly farming practices.
Used in Research:
GOSSYPLURE is also used in research settings to study the mating behavior and population dynamics of cotton bollworms and pink bollworms. Understanding the role of pheromones in these insects' reproductive processes can provide valuable insights into their biology and help develop more effective pest management strategies.
Used in Akebia trifoliata Seed Analysis:
GOSSYPLURE is a fatty acid component of the Akebia trifoliata seed, a plant species native to East Asia. Its presence in the seed can be analyzed and studied to better understand the chemical composition and potential applications of Akebia trifoliata seeds in various industries, such as pharmaceuticals or cosmetics.
Hazard
Extremely flammable.
Check Digit Verification of cas no
The CAS Registry Mumber 50933-33-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,9,3 and 3 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 50933-33:
(7*5)+(6*0)+(5*9)+(4*3)+(3*3)+(2*3)+(1*3)=110
110 % 10 = 0
So 50933-33-0 is a valid CAS Registry Number.
InChI:InChI=1/C18H32O2/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-20-18(2)19/h6-7,10-11H,3-5,8-9,12-17H2,1-2H3
50933-33-0Relevant academic research and scientific papers
Investigation of Aliphatic Dienes by Chemical Ionization with Nitric Oxide
Budzikiewicz, H.,Blech, St.,Schneider, B.
, p. 1057 - 1060 (2007/10/02)
It is shown that the position of the double bond close to the hydrocarbon end of an aliphatic diene functionalized at C(1) can readily be determined by chemical ionization with NO+.Owing to the low abundance of the ions characteristic for the position of the other double bond, its localization may be difficult.Measurement of the chemical ionization (nitric oxide as reagent gas) spectra of the corresponding epoxides or collision activation studies can help.
OZONOLYSIS OF ALKENES AND THE REACTIONS OF POLYFUNCTIONAL COMPOUNDS XL. SYNTHESIS OF (Z,Z)-, (E,E)-, AND (E/Z,Z/E)-7,11-HEXADECADIEN-1-YL ACETATES - COMPONENTS OF THE SEX PHEROMONE OF PECTINOPHORA GOSSYPIELLA (SAUNDERS)
Odinokov, V. N.,Mukhametzyanova, R. S.,Galeeva, R. I.,Ishmuratov, G. Yu.,Tolstikov, G. A.
, p. 1399 - 1407 (2007/10/02)
A new approach is proposed for the synthesis of (Z,Z)-, (E,E)-, and (E/Z,Z/E)-7,11-hexadecadien-1-yl acetates, which are components of the sex pheromone of the pink bollworm (Pectinophora Gossypiella).The method is based on the selective ozonolysis of (Z,Z,Z)-, (E,E,E), and (E,E,Z)-cyclododecatrienes.
