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Tricyclazol solution - analytical standard,100ug/ml in methanol, high purity , CAS No.41814-78-2

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Item Number
T110017
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T110017-1ml
1ml
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$54.90
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Bacterial (3013)

Basic Description

Synonyms TRICYCLAZOLE | 41814-78-2 | Tricyclazone | Beam | Blascide | Sivic | Pilarblas | Tricyclazol | Tizole | Trizole | Elanco 291 | Blas-T | 2,7,8,9-Tricyclazole | 8-methyl-[1,2,4]triazolo[3,4-b][1,3]benzothiazole | 5-Methyl[1,2,4]triazolo[3,4-b][1,3]benzothiazole | EL-291 | 5-Methyl-1,2,4-t
Specifications & Purity analytical standard, 100ug/ml in methanol
Shipped In Normal
Grade analytical standard

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Organoheterocyclic compounds
Class Benzotriazoles
Subclass Triazolobenzothiazoles
Intermediate Tree Nodes Not available
Direct Parent Triazolobenzothiazoles
Alternative Parents Benzothiazoles  Triazolothiazoles  Benzenoids  Triazoles  Thiazoles  Heteroaromatic compounds  Azacyclic compounds  Organopnictogen compounds  Organonitrogen compounds  Hydrocarbon derivatives  
Molecular Framework Aromatic heteropolycyclic compounds
Substituents Triazolobenzothiazole - 1,3-benzothiazole - Triazolothiazole - Benzenoid - Heteroaromatic compound - 1,2,4-triazole - Thiazole - Azole - Azacycle - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Organonitrogen compound - Aromatic heteropolycyclic compound
Description This compound belongs to the class of organic compounds known as triazolobenzothiazoles. These are compound containing a triazole ring fused to the benzene or the thiazole moiety of the benzothiazole ring system.
External Descriptors Pesticides

Associated Targets(non-human)

Alternaria solani (773 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Pyricularia grisea (1253 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Phytophthora capsici (336 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Trichoderma viride (1263 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Penicillium italicum (133 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Botrytis cinerea (4183 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Alternaria alternata (757 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Trichoderma harzianum (66 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Pyricularia oryzae (1832 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Penicillium crustosum (31 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Rhizoctonia solani (2251 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Sclerotinia sclerotiorum (877 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Nfe2l2 Nuclear factor erythroid 2-related factor 2 (214 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Sclerotinia minor (10 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Fusarium graminearum (1554 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Berkeleyomyces basicola (8 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Ustilaginoidea (18 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Mechanisms of Action

Mechanism of Action Action Type target ID Target Name Target Type Target Organism Binding Site Name References

Names and Identifiers

IUPAC Name 8-methyl-[1,2,4]triazolo[3,4-b][1,3]benzothiazole
INCHI InChI=1S/C9H7N3S/c1-6-3-2-4-7-8(6)12-5-10-11-9(12)13-7/h2-5H,1H3
InChIKey DQJCHOQLCLEDLL-UHFFFAOYSA-N
Smiles CC1=C2C(=CC=C1)SC3=NN=CN23
Isomeric SMILES CC1=C2C(=CC=C1)SC3=NN=CN23
WGK Germany 1
PubChem CID 39040
Molecular Weight 189.24
Beilstein 980261

Certificates(CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

3 results found

Lot Number Certificate Type Date Item
E2421505 Certificate of Analysis Apr 30, 2024 T110017
B2006061 Certificate of Analysis Sep 12, 2023 T110017
C1908125 Certificate of Analysis Nov 17, 2022 T110017

Chemical and Physical Properties

Molecular Weight 189.240 g/mol
XLogP3 1.700
Hydrogen Bond Donor Count 0
Hydrogen Bond Acceptor Count 3
Rotatable Bond Count 0
Exact Mass 189.036 Da
Monoisotopic Mass 189.036 Da
Topological Polar Surface Area 58.400 Ų
Heavy Atom Count 13
Formal Charge 0
Complexity 211.000
Isotope Atom Count 0
Defined Atom Stereocenter Count 0
Undefined Atom Stereocenter Count 0
Defined Bond Stereocenter Count 0
Undefined Bond Stereocenter Count 0
The total count of all stereochemical bonds 0
Covalently-Bonded Unit Count 1

Citations of This Product

1. Siyu Wei, Xinfang Wang, Xinyu Zhao, Ke Zhao, Linzhe Xu, Yingbo Chen.  (2023)  Detection of pesticide residues on flexible and transparent fluorinated polyimide film based on surface-enhanced Raman spectroscopy technology.  ANALYTICA CHIMICA ACTA,  1283  (341958). 
2. Niannian Cao, Jiawen Ji, Changsheng Li, Meng Yuan, Xuanjun Guo, Xingxing Zong, Liqin Li, Yongqiang Ma, Chen Wang, Sen Pang.  (2023)  Rapid and efficient removal of multiple aqueous pesticides by one-step construction boric acid modified biochar.  RSC Advances,  13  (13): (8765-8778). 
3. Xinying Duan, Li Zhang, Hongyan Si, Jie Song, Peng Wang, Shangxing Chen, Hai Luo, Xiaoping Rao, Zongde Wang, Shengliang Liao.  (2022)  Synthesis, Antifungal Activity, Cytotoxicity and QSAR Study of Camphor Derivatives.  Journal of Fungi,  (8): (762). 
4. Zihui Ma, Xiaoyan Liu, Yutong Liu, Wei Chen, Chengtao Wang.  (2022)  Studies on the biosynthetic pathways of melanin in Auricularia auricula.  JOURNAL OF BASIC MICROBIOLOGY,  62  (7): (843-856). 
5. Nisar Hussain, Hongbin Pu, Da-Wen Sun.  (2021)  Core size optimized silver coated gold nanoparticles for rapid screening of tricyclazole and thiram residues in pear extracts using SERS.  FOOD CHEMISTRY,  350  (129025). 
6. Shu Xu, Bi Wang, Linwei Li, Qian Zhou, Mei Tian, Xingzeng Zhao, Jian Peng, Fei Liu, Yu Chen, Yannan Xu, Xu Feng.  (2020)  Effects of camptothecin on the rice blast fungus Magnaporthe oryzae.  PESTICIDE BIOCHEMISTRY AND PHYSIOLOGY,  163  (108). 
7. Vu Van Cat, Ngo Xuan Dinh, Le Thi Tam, Nguyen Van Quy, Vu Ngoc Phan, Anh-Tuan Le.  (2019)  One-pot hydrothermal-synthesized rGO-Ag nanocomposite as a sensing platform for detection and quantification of methylene blue organic dye and tricyclazole pesticide.  Materials Today Communications,  21  (100639). 
8. Jiahe Wu, Fangyuan Li, Xi Hu, Jingxiong Lu, Xiaolian Sun, Jianqing Gao, Daishun Ling.  (2019)  Responsive Assembly of Silver Nanoclusters with a Biofilm Locally Amplified Bactericidal Effect to Enhance Treatments against Multi-Drug-Resistant Bacterial Infections.  ACS Central Science,  (8): (1366–1376). 
9. Xiaoyan Pei, Dazhen Xiong, Yuanchao Pei, Huiyong Wang, Jianji Wang.  (2018)  Switchable oil–water phase separation of ionic liquid-based microemulsions by CO2.  GREEN CHEMISTRY,  20  (18): (4236-4244). 
10. Kang Yan, Li Long, Chen Wanchao, Zhang Feiyu, Du Yiping, Wu Ting.  (2018)  Rapid In Situ SERS Analysis of Pesticide Residues on Plant Surfaces Based on Micelle Extraction of Targets and Stabilization of Ag Nanoparticle Aggregates.  Food Analytical Methods,  11  (11): (3161-3169). 
11. Gaoqiang Lv, Changwen Du, Fei Ma, Yazhen Shen, Jianmin Zhou.  (2018)  Rapid and Nondestructive Detection of Pesticide Residues by Depth-Profiling Fourier Transform Infrared Photoacoustic Spectroscopy.  ACS Omega,  (3): (3548–3553). 
12. Yu Zhang, Qin Guo, Sai An, Yifei Lu, Jianfeng Li, Xi He, Lisha Liu, Yujie Zhang, Tao Sun, Chen Jiang.  (2017)  ROS-Switchable Polymeric Nanoplatform with Stimuli-Responsive Release for Active Targeted Drug Delivery to Breast Cancer.  ACS Applied Materials & Interfaces,  (14): (12227–12240). 
13. Shijie Li, Sarun Juengpanich, Win Topatana, Tianao Xie, Lidan Hou, Yiyuan Zhu, Jiadong Chen, Yukai Shan, Yina Han, Ziyi Lu, Tianen Chen, Charlie Topatana, Bin Zhang, Jiasheng Cao, Jiahao Hu, Jiafei Yan, Yingxin Chen, Zhen Gu, Jicheng Yu, Xiujun Cai, Mingyu Chen.  (2024)  Adavosertib-encapsulated metal-organic frameworks for p53-mutated gallbladder cancer treatment via synthetic lethality.  Science Bulletin,  69  (1286). 
14. Fen Wang, Yingjian Hou.  (2024)  Adsorption of Tricyclazole and 2,4-Dichlorophenoxyacetic Acid onto Biochar Produced from Anaerobically Digested Sludge.  Water,  16  (18): (2697). 
15. Liwang Fei, Rahila Hafeez, Junliang Zhang, Shiquan Fu, Ying Xu, Lingyun Hao.  (2025)  Investigation of the mechanisms involved in the biocontrol activities of natural products from a marine soil bacterium against rice blast.  PEST MANAGEMENT SCIENCE,     

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