Fast Blue RR Salt - AR , CAS No.14726-29-5

CAS: 14726-29-5 Cat. No.: F100841 Molecular Weight: 387.89 EC Number: 238-777-5 PubChem CID: 2724074

GRADE & PURITY AR

Synonyms

Fast Blue RR Salt, crystalline | Azoic diazo component 24 | E78913 | AKOS015903985 | Azoic Diazo No. 24 | Fast Blue RR Salt, Preweighed Capsules | 4-Benzamido-2,5-dimethoxybenzenediazonium Salt Zinc Chloride | 4-benzamido-2,5-dimethoxybenzenediazonium;dic

Storage

Store at -20°C

Shipped In

Ice chest + Ice pads

Overview

Fast Blue RR Saltn is a useful dye to detect alkaline phosphatase and nonspecific esterase.

Product Application
Solid blue RR salts have been used in immunohistochemistry to detect alkaline phosphatase activity. It has been used in the connective tissue staining process using Sirius scarlet

Specifications

Synonyms

Fast Blue RR Salt, crystalline | Azoic diazo component 24 | E78913 | AKOS015903985 | Azoic Diazo No. 24 | Fast Blue RR Salt, Preweighed Capsules | 4-Benzamido-2, 5-dimethoxybenzenediazonium Salt Zinc Chloride | 4-benzamido-2, 5-dimethoxybenzenediazonium;dic

Specifications & Purity

AR

Storage

Store at -20°C

Shipped In

Ice chest + Ice pads

This product requires cold chain shipping. Ground and other economy services are not available.

Grade

AR

Names and Identifiers

• Pubchem Sid: 488192245
• Canonical Smiles: COC1=CC(=C(C=C1NC(=O)C2=CC=CC=C2)OC)[N+]#N.COC1=CC(=C(C=C1NC(=O)C2=CC=CC=C2)OC)[N+]#N.[Cl-].[Cl-].Cl[Zn]Cl
• IUPAC Name: 4-benzamido-2,5-dimethoxybenzenediazonium;dichlorozinc;dichloride
• InChIKey: LLARVKAOQLUCQI-UHFFFAOYSA-L
• INCHI: 1S/2C15H13N3O3.4ClH.Zn/c2*1-20-13-9-12(18-16)14(21-2)8-11(13)17-15(19)10-6-4-3-5-7-10;;;;;/h2*3-9H,1-2H3;4*1H;/q;;;;;;+2/p-2
• Isomeric SMILES: COC1=CC(=C(C=C1NC(=O)C2=CC=CC=C2)OC)[N+]#N.COC1=CC(=C(C=C1NC(=O)C2=CC=CC=C2)OC)[N+]#N.[Cl-].[Cl-].Cl[Zn]Cl
• WGK Germany: 3
• PubChem CID: 2724074
• Molecular Weight: 387.89

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Benzenoids
    • Class Benzene and substituted derivatives
      • Subclass Anilides
        • Level5 Aromatic anilides
          • Level6 Benzanilides

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Class: Benzene and substituted derivatives
• Subclass: Anilides
• Intermediate Tree Nodes: Aromatic anilides
• Direct Parent: Benzanilides
• Alternative Parents: Dimethoxybenzenes Methoxyanilines Benzamides Phenoxy compounds Benzoyl derivatives Anisoles Alkyl aryl ethers Secondary carboxylic acid amides Organic diazonium salts Organic transition metal salts Organopnictogen compounds Organic oxides Organic chloride salts Hydrocarbon derivatives
• Molecular Framework: Not available
• Substituents: Benzanilide - P-dimethoxybenzene - Dimethoxybenzene - Benzamide - Benzoic acid or derivatives - Methoxyaniline - Phenoxy compound - Anisole - Benzoyl - Methoxybenzene - Phenol ether - Alkyl aryl ether - Carboxamide group - Organic diazonium salt - Secondary carboxylic acid amide - Organic metal salt - Carboxylic acid derivative - Ether - Organic transition metal salt - Organopnictogen compound - Organic oxygen compound - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Organonitrogen compound - Organooxygen compound - Organic chloride salt - Organic salt - Aromatic homomonocyclic compound
• Description: This compound belongs to the class of organic compounds known as benzanilides. These are aromatic compounds containing an anilide group in which the carboxamide group is substituted with a benzene ring. They have the general structure RNC(=O)R', where R,R'= benzene.
• External Descriptors: Not available

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

Chemical and Physical Properties

• Solubility: Soluble in water (1 mg/ml).
• Molecular Weight: 775.800 g/mol
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 10
• Rotatable Bond Count: 8
• Exact Mass: 774.009 Da
• Monoisotopic Mass: 772.012 Da
• Topological Polar Surface Area: 151.000 Ų
• Heavy Atom Count: 47
• Formal Charge: 0
• Complexity: 403.000
• 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: 5

XLogP3

References

1. Jing-jing Xu, Yong-mei Chang, Mei Lu, Yuan Tie, Yan-ling Dong, Guang-you Chen, Zhi-qing Ma, Xi-li Liu, Yong-qiang Li.  (2021)  Two single mutations in carboxylesterase 001C improve fenvalerate hydrolase activity in Helicoverpa armigera.  PESTICIDE BIOCHEMISTRY AND PHYSIOLOGY,      [PMID:34802519] [10.1016/j.pestbp.2021.104969]

2. Li-Sha Bai, Jing-Jing Xu, Cai-Xia Zhao, Ya-Li Chang, Yan-Ling Dong, Kai-Ge Zhang, Yong-Qiang Li, Yi-Ping Li, Zhi-Qing Ma, Xi-Li Liu.  (2020)  Enhanced hydrolysis of β-cypermethrin caused by deletions in the glycin-rich region of carboxylesterase 001G from Helicoverpa armigera.  PEST MANAGEMENT SCIENCE,  77  (4): (2129-2141).  [PMID:33336552] [10.1002/ps.6242]

3. Yong-Qiang Li, Li-Sha Bai, Cai-Xia Zhao, Jing-Jing Xu, Zhong-Juan Sun, Yan-Ling Dong, De-Xian Li, Xi-Li Liu, Zhi-Qing Ma.  (2020)  Functional Characterization of Two Carboxylesterase Genes Involved in Pyrethroid Detoxification in Helicoverpa armigera.  JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY,      [PMID:32096985] [10.1021/acs.jafc.9b06690]

4. Li-sha Bai, Cai-xia Zhao, Jing-jing Xu, Chuan Feng, Yong-qiang Li, Yan-ling Dong, Zhi-qing Ma.  (2019)  Identification and biochemical characterization of carboxylesterase 001G associated with insecticide detoxification in Helicoverpa armigera.  PESTICIDE BIOCHEMISTRY AND PHYSIOLOGY,      [PMID:31153479] [10.1016/j.pestbp.2019.03.009]

5. Lu Xu, Jun Zhao, Yang Sun, Dejin Xu, Guangchun Xu, Xiaolong Xu, Yueliang Zhang, Shuijin Huang, Zhaojun Han, Zhongyan Gu.  (2018)  Constitutive overexpression of cytochrome P450 monooxygenase genes contributes to chlorantraniliprole resistance in Chilo suppressalis (Walker).  PEST MANAGEMENT SCIENCE,  75  (3): (718-725).  [PMID:30101471] [10.1002/ps.5171]

6. Yongqiang Li, Jianwei Liu, Mei Lu, Zhiqing Ma, Chongling Cai, Yonghong Wang, Xing Zhang.  (2016)  Bacterial Expression and Kinetic Analysis of Carboxylesterase 001D from Helicoverpa armigera.  INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES,  17  (4): (493).  [PMID:27049381] [10.3390/ijms17040493]

7. Yongmei Chang, Weihuan Xu, Shan Wang, Mengyao Zhu, Yanan Ru, Zhiheng Xu, Guangyou Chen, Yongqiang Li.  (2024)  Characterization of Four Carboxylesterases Involved in Detoxification of β-Cypermethrin, λ-Cyhalothrin, and Malathion in Helicoverpa armigera.  JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY,      [PMID:39508741] [10.1021/acs.jafc.4c07451]

8. Xuedi Zhang, Yue Zhang, Kai Xu, Jianhua Qin, Dehe Wang, Lijun Xu, Chuanwen Wang.  (2024)  Identification and biochemical characterization of a carboxylesterase gene associated with β-cypermethrin resistance in Dermanyssus gallinae.  POULTRY SCIENCE,      [PMID:38492248] [10.1016/j.psj.2024.103612]