Chromotrope FB - 10mM in DMSO , CAS No.3567-69-9

CAS: 3567-69-9 Cat. No.: C423604 Formula: C₂₀H₁₂N₂Na₂O₇S₂ Peso molecolare: 502.43 Numero EC: 222-657-4

GRADE & PURITY 10mM in DMSO

Synonyms

Carmoisine|3567-69-9|Acid red 14|C.I. Acid Red 14|Chromotrope FB|Azo Rubine|Azorubin|Acid Rubine|Brilliant Crimson Red|C.I. Food Red 3|azorubine|Karmesin|Nacarat|Carmoisine bss|Carmoisine ba|Carmoisine fu|Carmoisine ws|Carmoisine S|Carmoisine supra|Carmoi

Storage

Store at -80°C

Shipped In

Dry ice packs + Cold packs

Specifications

Sinonimi

Carmoisine | 3567-69-9 | Acid red 14 | C.I. Acid Red 14 | Chromotrope FB | Azo Rubine | Azorubin | Acid Rubine | Brilliant Crimson Red | C.I. Food Red 3 | azorubine | Karmesin | Nacarat | Carmoisine bss | Carmoisine ba | Carmoisine fu | Carmoisine ws | Carmoisine S | Carmoisine supra | Carmoi

Specifiche e purezza

10mM in DMSO

Condizioni di conservazione di stoccaggio

Store at -80°C

Spedito in

Dry ice packs + Cold packs

Questo prodotto richiede spedizione a catena fredda. I servizi di terra e altri servizi economici non sono disponibili.

Nomi e identificatori

• Pubchem Sid: 528776163
• Sorrisi canonici: C1=CC=C2C(=C1)C(=CC=C2S(=O)(=O)[O-])N=NC3=C(C4=CC=CC=C4C(=C3)S(=O)(=O)[O-])O.[Na+].[Na+]
• IUPAC Name: disodium;4-hydroxy-3-[(4-sulfonatonaphthalen-1-yl)diazenyl]naphthalene-1-sulfonate
• InChIKey: YSVBPNGJESBVRM-UHFFFAOYSA-L
• INCHI: 1S/C20H14N2O7S2.2Na/c23-20-15-8-4-3-7-14(15)19(31(27,28)29)11-17(20)22-21-16-9-10-18(30(24,25)26)13-6-2-1-5-12(13)16;;/h1-11,23H,(H,24,25,26)(H,27,28,29);;/q;2*+1/p-2
• Isomeri SMILES: C1=CC=C2C(=C1)C(=CC=C2S(=O)(=O)[O-])N=NC3=C(C4=CC=CC=C4C(=C3)S(=O)(=O)[O-])O.[Na+].[Na+]
• WGK Germania: 2
• RTECS: QK1925000
• Peso molecolare: 502.43
• Reaxy-Rn: 4121348
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=4121348&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Benzenoids
    • Classe Naphthalenes
      • Subclass Naphthalene sulfonic acids and derivatives
        • Level5 Naphthalene sulfonates
          • Level6 1-naphthalene sulfonates

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Classe: Naphthalenes
• Subclass: Naphthalene sulfonic acids and derivatives
• Intermediate Tree Nodes: Naphthalene sulfonates
• Direct Parent: 1-naphthalene sulfonates
• Alternative Parents: 1-naphthalene sulfonic acids and derivatives 1-sulfo,2-unsubstituted aromatic compounds Phenoxides Sulfonyls Organosulfonic acids Azo compounds Propargyl-type 1,3-dipolar organic compounds Organooxygen compounds Organic sodium salts Organic oxides Hydrocarbon derivatives Organic cations
• Molecular Framework: Aromatic homopolycyclic compounds
• Substituents: 1-naphthalene sulfonic acid or derivatives - 1-naphthalene sulfonate - Arylsulfonic acid or derivatives - 1-sulfo,2-unsubstituted aromatic compound - Phenoxide - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Organosulfonic acid - Sulfonyl - Azo compound - Organic alkali metal salt - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Organic sodium salt - Organic nitrogen compound - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Organic salt - Organic cation - Aromatic homopolycyclic compound
• Descrizione: This compound belongs to the class of organic compounds known as 1-naphthalene sulfonates. These are organic aromatic compounds that contain a naphthalene moiety that carries a sulfonic acid group at the 1-position. Naphthalene is a bicyclic compound that is made up of two fused 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

Meccanismi d'azione

Proprietà chimiche e fisiche

• Sensibilità: Moisture sensitive;light sensitive
• Punto di infiammabilità (°F): 437.0 °F
• Punto di infiammabilità (°C): > 225 °C
• Punto di fusione (°C): 275 °C；λmax：383 nm，515 nm (2nd)
• Peso molecolare: 502.400 g/mol
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 9
• Rotatable Bond Count: 2
• Exact Mass: 501.988 Da
• Monoisotopic Mass: 501.988 Da
• Topological Polar Surface Area: 176.000 Ų
• Heavy Atom Count: 33
• Formal Charge: 0
• Complexity: 854.000
• 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

Riferimenti

1. Weijun Xie, Yue Zhang, Lei Xu, Dan Xie, Li Jiang, Yanmao Dong, Yan Yuan.  (2023)  Degradation of Organic Dyes by the UCNP/h-BN/TiO2 Ternary Photocatalyst.  ACS Omega,      [PMID:38162774] [10.1021/acsomega.3c01899]

2. Zhaopeng Wang, Hui Lv, Yu Zhang, Yanan Li.  (2024)  A sensitive immunochromatography assay based on quantum dot nanobeads for determination of acid orange II.  JOURNAL OF FOOD COMPOSITION AND ANALYSIS,      [PMID:] [10.1016/j.jfca.2024.106485]

3. Xinmiao Xu, Yi Zhang, Yong Chen, Yu Liu.  (2024)  Vapor-Driven Crosslinked Hydroxypropyl-β-Cyclodextrin Electrospun Nanofibrous Membranes for Ultrafast Dye Removal.  Chemistry-Switzerland,  6  (4): (506-516).  [PMID:] [10.3390/chemistry6040029]

4. Shen Shen, Huimin Li, Jia jia Fu, Hong Bo Wang.  (2022)  Wastewater purification with different precursors of carbon dots dominated titanium dioxide: Mechanism insight.  JOURNAL OF ALLOYS AND COMPOUNDS,      [PMID:] [10.1016/j.jallcom.2022.166162]