Blue Tetrazolium - ≥95%(T) , CAS No.1871-22-3

CAS: 1871-22-3 Cat. No.: B105508 Peso molecular: 727.64 Beilstein Registry Number: 3894077 Número EC: 217-488-8

GRADE & PURITY ≥95%(T)

Synonyms

BTC | 2-[4-[4-(3,5-diphenyltetrazol-2-ium-2-yl)-3-methoxyphenyl]-2-methoxyphenyl]-3,5-diphenyltetrazol-2-ium;dichloride | 2H-Tetrazolium, 3,3'-(3,3'-dimethoxy-4,4'-biphenylylene)bis(2,5-diphenyl-, dichloride | 3,3'-Dianisolebis(4,4'-(3,5-diphenyl)tetrazol

Storage

Protected from light,Room temperature,Cool

Shipped In

Normal

Descripción general

Used in the assay of reducing sugars; Used in the preparation of DNA-cation complexes, immunoadsorbents for anti-DNA antibodies.

Specifications

Sinónimos

BTC | 2-[4-[4-(3, 5-diphenyltetrazol-2-ium-2-yl)-3-methoxyphenyl]-2-methoxyphenyl]-3, 5-diphenyltetrazol-2-ium;dichloride | 2H-Tetrazolium, 3, 3'-(3, 3'-dimethoxy-4, 4'-biphenylylene)bis(2, 5-diphenyl-, dichloride | 3, 3'-Dianisolebis(4, 4'-(3, 5-diphenyl)tetrazol

Especificaciones y pureza

≥95%(T)

Condiciones de almacenamiento de almacenamiento

Protected from light, Room temperature, Cool

Enviado en

Normal

Pureza

≥95%(T)

Nombres e identificadores

• Pubchem Sid: 488196366
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488196366
• Sonrisas canónicas: COC1=C(C=CC(=C1)C2=CC(=C(C=C2)N3N=C(N=[N+]3C4=CC=CC=C4)C5=CC=CC=C5)OC)N6N=C(N=[N+]6C7=CC=CC=C7)C8=CC=CC=C8.[Cl-].[Cl-]
• IUPAC Name: 2-[4-[4-(3,5-diphenyltetrazol-3-ium-2-yl)-3-methoxyphenyl]-2-methoxyphenyl]-3,5-diphenyltetrazol-3-ium;dichloride
• InChIKey: MUUHXGOJWVMBDY-UHFFFAOYSA-L
• INCHI: 1S/C40H32N8O2.2ClH/c1-49-37-27-31(23-25-35(37)47-43-39(29-15-7-3-8-16-29)41-45(47)33-19-11-5-12-20-33)32-24-26-36(38(28-32)50-2)48-44-40(30-17-9-4-10-18-30)42-46(48)34-21-13-6-14-22-34;;/h3-28H,1-2H3;2*1H/q+2;;/p-2
• Isómeros SMILES: COC1=C(C=CC(=C1)C2=CC(=C(C=C2)N3N=C(N=[N+]3C4=CC=CC=C4)C5=CC=CC=C5)OC)N6N=C(N=[N+]6C7=CC=CC=C7)C8=CC=CC=C8.[Cl-].[Cl-]
• WGK Alemania: 3
• Peso molecular: 727.64
• Beilstein: 3894077
• Reaxy-Rn: 3894077
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=3894077&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Benzenoids
    • Clase Benzene and substituted derivatives
      • Subclass Biphenyls and derivatives

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Clase: Benzene and substituted derivatives
• Subclass: Biphenyls and derivatives
• Intermediate Tree Nodes: Not available
• Direct Parent: Biphenyls and derivatives
• Alternative Parents: Phenyltetrazoles and derivatives Methoxyanilines Phenoxy compounds Methoxybenzenes Anisoles Alkyl aryl ethers Heteroaromatic compounds Azacyclic compounds Organopnictogen compounds Organonitrogen compounds Organic chloride salts Hydrocarbon derivatives
• Molecular Framework: Aromatic heteromonocyclic compounds
• Substituents: Biphenyl - Phenyltetrazole - Methoxyaniline - Phenoxy compound - Anisole - Phenol ether - Methoxybenzene - Alkyl aryl ether - Azole - Heteroaromatic compound - Tetrazole - Ether - Azacycle - Organoheterocyclic compound - Organic oxygen compound - Organooxygen compound - Organonitrogen compound - Organic nitrogen compound - Hydrocarbon derivative - Organopnictogen compound - Organic chloride salt - Organic salt - Aromatic heteromonocyclic compound
• Descripción: This compound belongs to the class of organic compounds known as biphenyls and derivatives. These are organic compounds containing to benzene rings linked together by a C-C bond.
• External Descriptors: organic chloride salt

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Objetivos asociados (no humanos)

Plasmodium falciparum (966862 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Mecanismos de acción

Propiedades químicas y físicas

• Solubilidad: Soluble in hot water (5 mg/ml), methanol (50 mg/ml), ethanol, and chloroform. Insoluble in acetone.
• Sensibilidad: light sensitive
• Punto de fusión (°C): 225°C
• Peso molecular: 727.600 g/mol
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 8
• Rotatable Bond Count: 9
• Exact Mass: 726.203 Da
• Monoisotopic Mass: 726.203 Da
• Topological Polar Surface Area: 87.600 Ų
• Heavy Atom Count: 52
• Formal Charge: 0
• Complexity: 951.000
• 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: 3

XLogP3

Referencias

1. Ximing Zhong, Guofeng Su, Qiye Zeng, Guangze Li, Hua Xu, Honghong Wu, Hongjun Zhou, Xinhua Zhou.  (2023)  Preparation of Salicylic Acid-Functionalized Nanopesticides and Their Applications in Enhancing Salt Stress Resistance.  ACS Applied Materials & Interfaces,      [PMID:37672316] [10.1021/acsami.3c06398]

2. Ping Zhang, Mingxue Xiang, Wei Jiang, Huiling Liu, Yu Chen, Ying Fang, Longyong Wu, Hongjun Guo, Yufei Wang.  (2023)  Configuration modulation of vermiculite by exfoliation coupled Cu(II) anchoring for boosting removal of tetracycline via synergy of adsorption and photocatalysis.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2023.145143]

3. Jun Zhao, Hanhan Wang, Hongqi Geng, Qi Yang, Yuping Tong, Weiwei He.  (2021)  Au/N-Doped Carbon Dot Nanozymes as Light-Controlled Anti- and Pro-Oxidants.  ACS Applied Nano Materials,      [PMID:] [10.1021/acsanm.1c01215]

4. Ze-Lin Qiu, Wen-Han Yu, Yu-Jie Shen, Bao-Ku Zhu, Li-Feng Fang.  (2021)  Cationic hyperbranched poly(amido-amine) engineered nanofiltration membrane for molecular separation.  JOURNAL OF MEMBRANE SCIENCE,      [PMID:] [10.1016/j.memsci.2021.119275]

5. Jiaqi Li, Mengxiao Zhang, Weilin Feng, Liping Zhu, Lin Zhang.  (2020)  PIM-1 pore-filled thin film composite membranes for tunable organic solvent nanofiltration.  JOURNAL OF MEMBRANE SCIENCE,      [PMID:] [10.1016/j.memsci.2020.117951]

6. Ming-Yong Zhou, Li-Feng Fang, Chuang-Chao Sun, Chun-Er Lin, Bao-Ku Zhu, Jiang-Hua Chen.  (2018)  Pore size tailoring from ultrafiltration to nanofiltration with PVC-g-PDMA via rapid immersion thermal annealing.  JOURNAL OF MEMBRANE SCIENCE,      [PMID:] [10.1016/j.memsci.2018.10.060]

7. Yisa Zhou, Ya Zhang, Jian Xue, Rui Wang, Jiale Dong, Zongjie Yin, Chen Guo, Haihui Wang.  (2024)  Electrochemically assisted preparation of graphitic carbon nitride nanosheet membranes for efficient water purification.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2024.151638]

8. Yaqi Dong, Haisheng Zhang, Xin Liu, Xinzhao Luo, Yanqiu Wang, Qiang Zhang.  (2024)  Quaternization and degradation of block copolymer templates for UF and ED membranes via non-solvent induced and solvent evaporation induced phase separation.  JOURNAL OF MEMBRANE SCIENCE,      [PMID:] [10.1016/j.memsci.2024.123156]

9. Yicheng Jiang, Shaobin Wen, Jingyu Zhang, Bin Peng, Haisheng Zhang, Qiang Zhang.  (2025)  Direct interfacial polymerization of cationic monosaccharides for nanofiltration membranes.  JOURNAL OF MEMBRANE SCIENCE,      [PMID:] [10.1016/j.memsci.2025.124525]