Alizarin yellow GG indicator - 0.1% , CAS No.584-42-9

CAS: 584-42-9 Cat. No.: A299263 Molecular Weight: 309.21 EC Number: 209-536-1 PubChem CID: 135442953

GRADE & PURITY 0.1%

Synonyms

A0123 | DTXSID8060402 | MFCD00044746 | AMY22366 | X-0950 | A0096 | Alizarine Yellow AGP | Showa Chrome Yellow GG | Hispacrom Yellow 2GR | Pontachrome Yellow GS | Calcochrome Yellow 2G | Y1YL31LOKF | Alizarine Yellow 2G | RV 1 | Alizarine Yellow GG | Sodiu

Storage

Room temperature

Shipped In

Normal

Specifications

Synonyms

A0123 | DTXSID8060402 | MFCD00044746 | AMY22366 | X-0950 | A0096 | Alizarine Yellow AGP | Showa Chrome Yellow GG | Hispacrom Yellow 2GR | Pontachrome Yellow GS | Calcochrome Yellow 2G | Y1YL31LOKF | Alizarine Yellow 2G | RV 1 | Alizarine Yellow GG | Sodiu

Specifications & Purity

0.1%

Biochemical and Physiological Mechanisms

Acid-base indicator for nutrient media preparation. pH range 10.1 (yellow) to 12.0 (red).

Storage

Room temperature

Shipped In

Normal

Note

Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.

Names and Identifiers

• Canonical Smiles: C1=CC(=CC(=C1)[N+](=O)[O-])N=NC2=CC(=C(C=C2)[O-])C(=O)O.[Na+]
• IUPAC Name: sodium;2-carboxy-4-[(3-nitrophenyl)diazenyl]phenolate
• InChIKey: ZHFPEICFUVWJIS-UHFFFAOYSA-M
• INCHI: 1S/C13H9N3O5.Na/c17-12-5-4-9(7-11(12)13(18)19)15-14-8-2-1-3-10(6-8)16(20)21;/h1-7,17H,(H,18,19);/q;+1/p-1
• Isomeric SMILES: C1=CC(=CC(=C1)[N+](=O)[O-])N=NC2=CC(=C(C=C2)[O-])C(=O)O.[Na+]
• PubChem CID: 135442953
• Molecular Weight: 309.21

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organoheterocyclic compounds
    • Class Azobenzenes

• Kingdom: Organic compounds
• Superclass: Organoheterocyclic compounds
• Class: Azobenzenes
• Subclass: Not available
• Intermediate Tree Nodes: Not available
• Direct Parent: Azobenzenes
• Alternative Parents: Nitrobenzenes Benzoic acids Nitroaromatic compounds Benzoyl derivatives Phenoxides Vinylogous acids Azo compounds Propargyl-type 1,3-dipolar organic compounds Organic oxoazanium compounds Carboxylic acids Organooxygen compounds Organic zwitterions Organic sodium salts Organic oxides Hydrocarbon derivatives
• Molecular Framework: Aromatic homomonocyclic compounds
• Substituents: Azobenzene - Benzoic acid or derivatives - Benzoic acid - Nitrobenzene - Nitroaromatic compound - Benzoyl - Phenoxide - Monocyclic benzene moiety - Benzenoid - Vinylogous acid - Azo compound - Organic nitro compound - C-nitro compound - Allyl-type 1,3-dipolar organic compound - Carboxylic acid - Propargyl-type 1,3-dipolar organic compound - Organic 1,3-dipolar compound - Carboxylic acid derivative - Organic alkali metal salt - Organic oxoazanium - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Organic zwitterion - Organic salt - Organic sodium salt - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Aromatic homomonocyclic compound
• Description: This compound belongs to the class of organic compounds known as azobenzenes. These are organonitrogen aromatic compounds that contain a central azo group, where each nitrogen atom is conjugated to a benzene ring.
• 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

Mechanisms of Action

Chemical and Physical Properties

• Molecular Weight: 309.210 g/mol
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 7
• Rotatable Bond Count: 3
• Exact Mass: 309.036 Da
• Monoisotopic Mass: 309.036 Da
• Topological Polar Surface Area: 131.000 Ų
• Heavy Atom Count: 22
• Formal Charge: 0
• Complexity: 423.000
• 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: 2

XLogP3

References

1. Han-Qing Zhao, Nannan Hou, Yi-Ran Wang, Wen-Qiang Li, Qi Liu, Peili Lu, Yang Mu.  (2022)  Carbon nanotubes mediated chemical and biological decolorization of azo dye: Understanding the structure-activity relationship.  ENVIRONMENTAL RESEARCH,      [PMID:35151661] [10.1016/j.envres.2022.112897]

2. Yanqing Xu, Suyang Yu, Guibin Peng, Arcadio Sotto, Huimin Ruan, Jiangnan Shen, Congjie Gao.  (2020)  Novel crosslinked brominated polyphenylene oxide composite nanofiltration membranes with organic solvent permeability and swelling property.  JOURNAL OF MEMBRANE SCIENCE,      [PMID:] [10.1016/j.memsci.2020.118784]

3. Siqi Liu, Xiaolin Xu, Yanshun Kang, Yingtian Xiao, Huan Liu.  (2020)  Degradation and detoxification of azo dyes with recombinant ligninolytic enzymes from Aspergillus sp. with secretory overexpression in Pichia pastoris.  Royal Society Open Science,  7  (9):   [PMID:33047030] [10.1098/rsos.200688]