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Naphthol Green B - Biological stain, high purity , CAS No.19381-50-1
Basic Description
Synonyms
Naphthol Green B (C.I. 10020) | trisodium;6-hydroxy-5-nitrosonaphthalene-2-sulfonate;iron | AKOS015903070 | sodium tris(1-nitroso-6-sulfonatonaphthalen-2-yloxy)iron | MFCD00003886 | AKOS025310849 | Naphthol Green B, Technical grade | Naphthol Green B
Specifications & Purity
Biological stain
Storage Temp
Protected from light
Shipped In
Normal
Grade
Biological Stain
Taxonomic Classification
Kingdom
Organic compounds
Superclass
Benzenoids
Class
Naphthalenes
Subclass
Naphthalene sulfonic acids and derivatives
Intermediate Tree Nodes
Naphthalene sulfonates
Direct Parent
2-naphthalene sulfonates
Alternative Parents
2-naphthalene sulfonic acids and derivatives Naphthols and derivatives 1-sulfo,2-unsubstituted aromatic compounds Phenoxides 1-hydroxy-2-unsubstituted benzenoids Sulfonyls Organosulfonic acids Propargyl-type 1,3-dipolar organic compounds Organic transition metal salts C-nitroso compounds Organooxygen compounds Organic sodium salts Organic oxides Hydrocarbon derivatives Organic cations
Molecular Framework
Not available
Substituents
2-naphthalene sulfonic acid or derivatives - 2-naphthalene sulfonate - 2-naphthol - Arylsulfonic acid or derivatives - 1-sulfo,2-unsubstituted aromatic compound - Phenol - Phenoxide - 1-hydroxy-2-unsubstituted benzenoid - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Sulfonyl - Organosulfonic acid - Organic alkali metal salt - Organic transition metal salt - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Organic nitroso compound - C-nitroso compound - Hydrocarbon derivative - Organic sodium salt - Organic oxygen compound - Organic oxide - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Organic nitrogen compound - Organic salt - Organic cation - Aromatic homopolycyclic compound
Description
This compound belongs to the class of organic compounds known as 2-naphthalene sulfonates. These are organic aromatic compounds that contain a naphthalene moiety that carries a sulfonic acid group at the 2-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.
Names and Identifiers
Pubchem Sid
504767679
Pubchem Sid Url
https://pubchem.ncbi.nlm.nih.gov/substance/504767679
IUPAC Name
trisodium;6-hydroxy-5-nitrosonaphthalene-2-sulfonate;iron
INCHI
InChI=1S/3C10H7NO5S.Fe.3Na/c3*12-9-4-1-6-5-7(17(14,15)16)2-3-8(6)10(9)11-13;;;;/h3*1-5,12H,(H,14,15,16);;;;/q;;;;3*+1/p-3
InChIKey
VLBLPLXOYXEXJK-UHFFFAOYSA-K
Smiles
C1=CC2=C(C=CC(=C2N=O)O)C=C1S(=O)(=O)[O-].C1=CC2=C(C=CC(=C2N=O)O)C=C1S(=O)(=O)[O-].C1=CC2=C(C=CC(=C2N=O)O)C=C1S(=O)(=O)[O-].[Na+].[Na+].[Na+].[Fe]
Isomeric SMILES
C1=CC2=C(C=CC(=C2N=O)O)C=C1S(=O)(=O)[O-].C1=CC2=C(C=CC(=C2N=O)O)C=C1S(=O)(=O)[O-].C1=CC2=C(C=CC(=C2N=O)O)C=C1S(=O)(=O)[O-].[Na+].[Na+].[Na+].[Fe]
WGK Germany
1
RTECS
LJ8930000
PubChem CID
14598749
Molecular Weight
878.46
Beilstein
11332
Reaxy-Rn
14313514
Certificates（CoA,COO,BSE/TSE and Analysis Chart)
Chemical and Physical Properties
Sensitivity
Light sensitive.
Molecular Weight
881.500 g/mol
XLogP3
Hydrogen Bond Donor Count
3
Hydrogen Bond Acceptor Count
18
Rotatable Bond Count
0
Exact Mass
880.894 Da
Monoisotopic Mass
880.894 Da
Topological Polar Surface Area
346.000 Ų
Heavy Atom Count
55
Formal Charge
0
Complexity
1320.000
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
7
Citations of This Product
1.
Jufen Yan, Pei Wang, Longxin Wang, Qi Jin, Abdallah S. Ali, Yongsheng He, Ying Wang, Yuxuan Sun, Aoqiang Li, Waly Adwy, Rasha H. Ahmed, Xinya Han.
(2023)
Bio-decolorization of synthetic dyes by a novel endophytic fungus Penicillium janthinellum LM5 from blueberry pulp. BIOCHEMICAL ENGINEERING JOURNAL,
195
(108909).
2.
Zhipeng Du, Jiajun Chen, Shengnan Ke, Qi Xu, Zhenquan Wang.
(2023)
Experimental investigations on spreading and displacement of fluid plumes around an injection well in a contaminated aquifer. JOURNAL OF HYDROLOGY,
617
(129062).
3.
Sixian Liu, Nian Jiang, Yuquan Chi, Qiang Peng, Guoru Dai, Ling Qian, Keming Xu, Wenying Zhong, Wanqing Yue.
(2022)
Injectable and Self-Healing Hydrogel Based on Chitosan-Tannic Acid and Oxidized Hyaluronic Acid for Wound Healing. ACS Biomaterials Science & Engineering,
8
(9):
(3754–3764).
4.
Jinyi Zhang, Jing Zuo, Yinshan Jiang, Dandan Zhu, Jiupeng Zhang, Cundi Wei.
(2020)
Kinetic analysis on the mesoporous formation of coal gasification slag by acid leaching and its thermal stability. SOLID STATE SCIENCES,
100
(106084).
5.
Yiwen Li, Cuicui Hu, Shikuan Xu, Qi Guo, Pengfei Qi, Rong Li, Yanjun Xing.
(2024)
ZIF-8 metal-organic network/poly(vinyl alcohol) composite for adsorptive removal of various organic dyes. MATERIALS CHEMISTRY AND PHYSICS,
315
(129009).
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5 Citations
L2405089