TiadinilCAS# 223580-51-6 |
2D Structure
- BS-181 HCl
Catalog No.:BCC2537
CAS No.:1397219-81-6
- PHA-793887
Catalog No.:BCC2521
CAS No.:718630-59-2
- PHA-848125
Catalog No.:BCC3839
CAS No.:802539-81-7
Quality Control & MSDS
3D structure
Package In Stock
Number of papers citing our products
Cas No. | 223580-51-6 | SDF | Download SDF |
PubChem ID | 2804318 | Appearance | Powder |
Formula | C11H10ClN3OS | M.Wt | 267.73 |
Type of Compound | N/A | Storage | Desiccate at -20°C |
Synonyms | AK163155 | ||
Solubility | Soluble in DMSO | ||
Chemical Name | N-(3-chloro-4-methylphenyl)-4-methylthiadiazole-5-carboxamide | ||
SMILES | CC1=C(C=C(C=C1)NC(=O)C2=C(N=NS2)C)Cl | ||
Standard InChIKey | VJQYLJSMBWXGDV-UHFFFAOYSA-N | ||
Standard InChI | InChI=1S/C11H10ClN3OS/c1-6-3-4-8(5-9(6)12)13-11(16)10-7(2)14-15-17-10/h3-5H,1-2H3,(H,13,16) | ||
General tips | For obtaining a higher solubility , please warm the tube at 37 ℃ and shake it in the ultrasonic bath for a while.Stock solution can be stored below -20℃ for several months. We recommend that you prepare and use the solution on the same day. However, if the test schedule requires, the stock solutions can be prepared in advance, and the stock solution must be sealed and stored below -20℃. In general, the stock solution can be kept for several months. Before use, we recommend that you leave the vial at room temperature for at least an hour before opening it. |
||
About Packaging | 1. The packaging of the product may be reversed during transportation, cause the high purity compounds to adhere to the neck or cap of the vial.Take the vail out of its packaging and shake gently until the compounds fall to the bottom of the vial. 2. For liquid products, please centrifuge at 500xg to gather the liquid to the bottom of the vial. 3. Try to avoid loss or contamination during the experiment. |
||
Shipping Condition | Packaging according to customer requirements(5mg, 10mg, 20mg and more). Ship via FedEx, DHL, UPS, EMS or other couriers with RT, or blue ice upon request. |
Description | Tiadinil is a plant activator of systemic acquired resistance, boosts the production of herbivore-induced plant volatiles; insecticide agent. References: |
Tiadinil Dilution Calculator
Tiadinil Molarity Calculator
1 mg | 5 mg | 10 mg | 20 mg | 25 mg | |
1 mM | 3.7351 mL | 18.6755 mL | 37.3511 mL | 74.7021 mL | 93.3777 mL |
5 mM | 0.747 mL | 3.7351 mL | 7.4702 mL | 14.9404 mL | 18.6755 mL |
10 mM | 0.3735 mL | 1.8676 mL | 3.7351 mL | 7.4702 mL | 9.3378 mL |
50 mM | 0.0747 mL | 0.3735 mL | 0.747 mL | 1.494 mL | 1.8676 mL |
100 mM | 0.0374 mL | 0.1868 mL | 0.3735 mL | 0.747 mL | 0.9338 mL |
* Note: If you are in the process of experiment, it's necessary to make the dilution ratios of the samples. The dilution data above is only for reference. Normally, it's can get a better solubility within lower of Concentrations. |
Calcutta University
University of Minnesota
University of Maryland School of Medicine
University of Illinois at Chicago
The Ohio State University
University of Zurich
Harvard University
Colorado State University
Auburn University
Yale University
Worcester Polytechnic Institute
Washington State University
Stanford University
University of Leipzig
Universidade da Beira Interior
The Institute of Cancer Research
Heidelberg University
University of Amsterdam
University of Auckland
TsingHua University
The University of Michigan
Miami University
DRURY University
Jilin University
Fudan University
Wuhan University
Sun Yat-sen University
Universite de Paris
Deemed University
Auckland University
The University of Tokyo
Korea University
Tiadinil is a plant activator of systemic acquired resistance, boosts the production of herbivore-induced plant volatiles; insecticide agent.
- CPA inhibitor
Catalog No.:BCC1500
CAS No.:223532-02-3
- YM 58483
Catalog No.:BCC7817
CAS No.:223499-30-7
- ONO 4817
Catalog No.:BCC2375
CAS No.:223472-31-9
- GLP-2 (human)
Catalog No.:BCC5891
CAS No.:223460-79-5
- FG2216
Catalog No.:BCC6402
CAS No.:223387-75-5
- Polygalacic acid
Catalog No.:BCN5898
CAS No.:22338-71-2
- Grandifloric acid
Catalog No.:BCN4669
CAS No.:22338-69-8
- Grandiflorenic acid
Catalog No.:BCN4670
CAS No.:22338-67-6
- 9-Hydroxy-alpha-lapachone
Catalog No.:BCN5060
CAS No.:22333-58-0
- Methyl ferulate
Catalog No.:BCN4023
CAS No.:22329-76-6
- Platycodigenin
Catalog No.:BCN3183
CAS No.:22327-82-8
- Evodol
Catalog No.:BCN5059
CAS No.:22318-10-1
- K-115 free base
Catalog No.:BCC5501
CAS No.:223645-67-8
- Collagen proline hydroxylase inhibitor-1
Catalog No.:BCC1495
CAS No.:223663-32-9
- Collagen proline hydroxylase inhibitor
Catalog No.:BCC1494
CAS No.:223666-07-7
- Mirabegron (YM178)
Catalog No.:BCC3814
CAS No.:223673-61-8
- Eupatilin
Catalog No.:BCN2336
CAS No.:22368-21-4
- 4-Methoxysalicylic acid
Catalog No.:BCN7783
CAS No.:2237-36-7
- Sodium Monensin
Catalog No.:BCC5319
CAS No.:22373-78-0
- NPE-caged-HPTS
Catalog No.:BCC5950
CAS No.:223759-19-1
- Bestatin trifluoroacetate
Catalog No.:BCC3909
CAS No.:223763-80-2
- Pedalitin
Catalog No.:BCN3954
CAS No.:22384-63-0
- Serratenediol
Catalog No.:BCN5061
CAS No.:2239-24-9
- 3,8-Di-O-methylellagic acid
Catalog No.:BCN5062
CAS No.:2239-88-5
Determination of tiadinil and its metabolite in flue-cured tobacco.[Pubmed:23825350]
J Chromatogr Sci. 2014 Aug;52(7):624-8.
A novel and sensitive method was developed for the determination of residues of Tiadinil and its metabolite, 4-methyl-l,2,3-thiadiazole-5-carboxylic acid, in flue-cured tobacco. The pesticides were extracted with acetone and purified by gel permeation chromatography and solid-phase extraction. Analysis was performed by ultra-performance liquid chromatography-tandem mass spectrometry in negative ionization mode. Two precursor-product ion transitions were monitored for both compounds in the multiple reaction monitoring mode. Quantification was conducted by using matrix-matched standard calibration. Recovery values of the proposed method for Tiadinil ranged from 72.5 to 98.2%, with relative standard deviations ranging from 3.8 to 9.5%; recovery values for 4-methyl-l,2,3-thiadiazole-5-carboxylic acid ranged from 75.4 to 103.3% with RSDs ranging from 3.7 to 9.3%. The limit of quantification for both compounds was 0.01 mg/kg. This method is valuable for residual analysis, quality control and monitoring of Tiadinil and its metabolite, 4-methyl-l,2,3-thiadiazole-5-carboxylic acid, in tobacco.
Tiadinil, a plant activator of systemic acquired resistance, boosts the production of herbivore-induced plant volatiles that attract the predatory mite Neoseiulus womersleyi in the tea plant Camellia sinensis.[Pubmed:22669277]
Exp Appl Acarol. 2012 Nov;58(3):247-58.
Plants respond with various defense mechanisms to pathogenic or herbivorous attack. Some chemicals called plant activators that induce the plant defense response against pathogens have been commercially used to protect plants. Here we studied the effects of Tiadinil (TDL) on defense mechanisms against herbivores. TDL suppresses pathogenic fungi on tea leaves by inducing defense mechanisms. We used one of the major trophic systems in tea consisting of the herbivorous mite, Tetranychus kanzawai, and the predatory mite, Neoseiulus womersleyi. TDL enhanced the production of herbivore-induced plant volatiles that attract predatory mites. The predatory mites preferred the T. kanzawai-induced volatiles from TDL-treated plants to those produced by untreated plants. These results suggest that TDL activates the plant defense response via an indirect process mediated by plant volatiles that attract natural enemies of the herbivores. In contrast, the oviposition rate, adult maturation rate, and sex ratio of T. kanzawai were not affected by TDL treatment. These results suggest that TDL did not activate any direct defense against the herbivorous mite.