65410-38-0 Usage
Description
Traumatin is a bioactive compound that serves as a wound hormone in plants, playing a crucial role in their defense mechanisms against various stressors. It is the oxidation product of polyunsaturated fatty acids, such as Linoleic Acid (L467495), and is involved in the regulation of plant growth and development.
Uses
Used in Plant Defense Mechanisms:
Traumatin is used as a wound hormone in plants for its ability to trigger a defense response against various stressors, such as physical damage, pathogens, and environmental factors. It helps in the activation of signaling pathways that lead to the production of protective compounds and the repair of damaged tissues.
Used in Plant Growth Regulation:
Traumatin is used as a growth regulator in plants for its role in modulating various growth and developmental processes. It influences cell division, elongation, and differentiation, contributing to the overall growth and development of the plant.
Used in Plant Stress Tolerance:
Traumatin is used as a stress tolerance enhancer in plants for its ability to improve their resistance to various biotic and abiotic stressors. It helps in the activation of stress-responsive genes and the production of stress-protective compounds, thereby increasing the plant's ability to withstand adverse conditions.
Used in Plant Hormone Research:
Traumatin is used as a research tool in the study of plant hormones and their role in growth regulation, stress response, and defense mechanisms. It provides valuable insights into the complex signaling networks that govern plant growth and development, as well as their ability to adapt to changing environmental conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 65410-38-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,4,1 and 0 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 65410-38:
(7*6)+(6*5)+(5*4)+(4*1)+(3*0)+(2*3)+(1*8)=110
110 % 10 = 0
So 65410-38-0 is a valid CAS Registry Number.
InChI:InChI=1/C12H20O3/c13-11-9-7-5-3-1-2-4-6-8-10-12(14)15/h7,9,11H,1-6,8,10H2,(H,14,15)/b9-7+
65410-38-0Relevant articles and documents
UV Lamp as a Facile Ozone Source for Structural Analysis of Unsaturated Lipids Via Electrospray Ionization-Mass Spectrometry
Stinson, Craig A.,Zhang, Wenpeng,Xia, Yu
, p. 481 - 489 (2018/03/09)
Ozonolysis of alkene functional groups is a type of highly specific and effective chemical reaction, which has found increasing applications in structural analysis of unsaturated lipids via coupling with mass spectrometry (MS). In this work, we utilized a low-pressure mercury lamp (6?W) to initiate ozonolysis inside electrospray ionization (ESI) sources. By placing the lamp near a nanoESI emitter that partially transmits 185?nm ultraviolet (UV) emission from the lamp, dissolved dioxygen in the spray solution was converted into ozone, which subsequently cleaved the double bonds within fatty acyls of lipids. Solvent conditions, such as presence of water and acid solution pH, were found to be critical in optimizing ozonolysis yields. Fast (on seconds time scale) and efficient (50%–100% yield) ozonolysis was achieved for model unsaturated phospholipids and fatty acids with UV lamp-induced ozonolysis incorporated on a static and an infusion nanoESI source. The method was able to differentiate double bond location isomers and identify the geometry of the double bond based on yield. The analytical utility of UV lamp-induced ozonolysis was further demonstrated by implementation on a liquid chromatography (LC)-MS platform. Ozonolysis was effected in a flow microreactor that was made from ozone permeable tubing, so that ambient ozone produced by the lamp irradiation could diffuse into the reactor and induce online ozonolysis post-LC separation and before ESI-MS. [Figure not available: see fulltext.].
