9,10-Diphenylanthracene - analytical standard , CAS No.1499-10-1

CAS: 1499-10-1 Cat. No.: D106410 Peso molecular: 330.42 Beilstein Registry Number: 1914010 Número EC: 216-105-1
Disponible para pedir
GRADE & PURITY Analytical standard ? Analytical standard — certified-purity material for quantitative calibration. Use to prepare calibration standards and validate analytical methods.
Synonyms
A808976 | D1689 | NSC24861 | C26H18 | AKOS004902510 | Q274986 | SY015328 | D4401 | 9,10-diphenyl anthracene | EINECS 216-105-1 | 51BQ8IYQ9U | 9,10-Diphenylanthracene, analytical standard | Anthracene,10-diphenyl- | 9,10-Diphenylanthracene, 97% | Anthracen
Storage
Room temperature
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250mg
D106410-250mg
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159,90US$

185,90US$
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Why this grade

analytical standard Analytical standard for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Room temperature Ships Normal Check lot-specific COA for exact specifications.

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Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

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Literature proof

Cited in 43 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Sinónimos
A808976 | D1689 | NSC24861 | C26H18 | AKOS004902510 | Q274986 | SY015328 | D4401 | 9, 10-diphenyl anthracene | EINECS 216-105-1 | 51BQ8IYQ9U | 9, 10-Diphenylanthracene, analytical standard | Anthracene, 10-diphenyl- | 9, 10-Diphenylanthracene, 97% | Anthracen
Especificaciones y pureza
analytical standard
Condiciones de almacenamiento de almacenamiento
Room temperature
Enviado en
Normal
Grado
Analytical standard
Nombres e identificadores
Sonrisas canónicasC1=CC=C(C=C1)C2=C3C=CC=CC3=C(C4=CC=CC=C42)C5=CC=CC=C5
IUPAC Name9,10-diphenylanthracene
InChIKeyFCNCGHJSNVOIKE-UHFFFAOYSA-N
INCHI1S/C26H18/c1-3-11-19(12-4-1)25-21-15-7-9-17-23(21)26(20-13-5-2-6-14-20)24-18-10-8-16-22(24)25/h1-18H
Isómeros SMILES C1=CC=C(C=C1)C2=C3C=CC=CC3=C(C4=CC=CC=C42)C5=CC=CC=C5
WGK Alemania 3
RTECS CB0545500
Peso molecular 330.42
Beilstein 1914010
Reaxy-Rn 1914010
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1914010&ln=

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

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✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

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📊 Datasheet

Quick-reference summary of product specifications and applications.

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🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

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Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassLignans, neolignans and related compounds
ClaseArylnaphthalene lignans
SubclassNot available
Intermediate Tree Nodes Not available
Direct ParentArylnaphthalene lignans
Alternative Parents Anthracenes  Benzene and substituted derivatives  Aromatic hydrocarbons  Polycyclic hydrocarbons  Unsaturated hydrocarbons  
Molecular FrameworkAromatic homopolycyclic compounds
Substituents Arylnaphthalene lignan skeleton - Anthracene - Benzenoid - Monocyclic benzene moiety - Aromatic hydrocarbon - Polycyclic hydrocarbon - Unsaturated hydrocarbon - Hydrocarbon - Aromatic homopolycyclic compound
DescripciónThis compound belongs to the class of organic compounds known as arylnaphthalene lignans. These are lignans containing the arylnaphthalene skeleton, especially 9-(2H-1,3-benzodioxol-5-yl)-1H,3H-naphtho[2,3-c]furan-1-one or a derivative thereof. Arylnaphthalene lignans occur in nature and exhibit diverse biological activities.
External Descriptors anthracenes
Estructura 3D
Modelo de Estructura Química Interactiva





Certificados (CoA, COO, BSE/TSE y tabla de análisis)
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Analytical Chart:

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1 results found

Lot NumberCertificate TypeFechaArticulo
G1205050Certificate of AnalysisSep 16, 2025 D106410
Propiedades químicas y físicas
Punto de ebullición (°C)469.1ºC
Punto de fusión (°C)245-248°C
Peso molecular330.400 g/mol
XLogP37.600
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count0
Rotatable Bond Count2
Exact Mass330.141 Da
Monoisotopic Mass330.141 Da
Topological Polar Surface Area0.000 Ų
Heavy Atom Count26
Formal Charge0
Complexity375.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Citations of This Product
Referencias
1. Junjie Zhang, Yongjia Hong, Xu Tang, Yong Chen, Wenran Gao, Yuncheng Cai, Ningning Dong, Jiazi Xu, Li Zhang, Quli Fan, Bin Sun.  (2023)  Sulfur-nitrogen synergistic active sites enable continuous and fast removal of organic pollutants in practical water matrix.  SEPARATION AND PURIFICATION TECHNOLOGY,      [PMID:] [10.1016/j.seppur.2023.125817]
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4. Xiaoxiao Gu, Lixian Xu, Haoyang Yuan, Cailing Li, Juan Zhao, Shuang Li, Dinghua Yu.  (2023)  Sophorolipid-toluidine blue conjugates for improved antibacterial photodynamic therapy through high accumulation.  RSC Advances,  13  (17): (11782-11793).  [PMID:37077994] [10.1039/D3RA01618H]
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8. Xianhu Long, Zhaokun Xiong, Rongfu Huang, Yahan Yu, Peng Zhou, Heng Zhang, Gang Yao, Bo Lai.  (2022)  Sustainable Fe(III)/Fe(II) cycles triggered by co-catalyst of weak electrical current in Fe(III)/peroxymonosulfate system: Collaboration of radical and non-radical mechanisms.  APPLIED CATALYSIS B-ENVIRONMENTAL,      [PMID:] [10.1016/j.apcatb.2022.121716]
9. Qiang Fu, Jiaqiang Rui, Jiaojiao Fang, Yaru Ni, Liang Fang, Chunhua Lu, Zhongzi Xu.  (2022)  Triplet-Triplet Annihilation Up-Conversion Luminescent Assisted Free-Radical Reactions of Polymers Using Visible Light.  MACROMOLECULAR CHEMISTRY AND PHYSICS,  223  (14): (2200038).  [PMID:] [10.1002/macp.202200038]
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11. Chao Nan Zhu, Si Yu Zheng, Hao Nan Qiu, Cong Du, Miao Du, Zi Liang Wu, Qiang Zheng.  (2021)  Plastic-Like Supramolecular Hydrogels with Polyelectrolyte/Surfactant Complexes as Physical Cross-links.  MACROMOLECULES,      [PMID:] [10.1021/acs.macromol.1c00835]
12. Juan Zhao, Lixian Xu, Hao Zhang, Yuhong Zhuo, Yanan Weng, Shuang Li, Dinghua Yu.  (2021)  Surfactin-methylene blue complex under LED illumination for antibacterial photodynamic therapy: Enhanced methylene blue transcellular accumulation assisted by surfactin.  COLLOIDS AND SURFACES B-BIOINTERFACES,      [PMID:34303113] [10.1016/j.colsurfb.2021.111974]
13. Ying Cai, Shihao Shen, Jinhong Fan.  (2021)  Enhanced degradation of tetracycline by Cu(II) complexation in the FeS/sulfite system.  JOURNAL OF HAZARDOUS MATERIALS,      [PMID:34330076] [10.1016/j.jhazmat.2021.126673]
14. Xiao-Pan Liu, Wen-Qian Sun, Tong-Xin Liu, Bing-Bing Liu, Chang-Po Chen.  (2021)  Fullerenol as a water-soluble MALDI-MS matrix for rapid analysis of small molecules and efficient quantification of saccharin sodium in foods.  JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES,      [PMID:34130205] [10.1016/j.jchromb.2021.122819]
15. Xue Li, Wenting Liu, Jiaojiao Fang, Hengming Huang, Cheng Zhu, Yaru Ni, Liang Fang, Jiahui Kou, Chunhua Lu, Zhongzi Xu.  (2021)  Dual-layered up-conversion films with tunable multi-peaks spectrum for efficient photocatalytic degradation.  JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY A-CHEMISTRY,      [PMID:] [10.1016/j.jphotochem.2021.113360]
16. Yuan-Fu Ding, Cheryl H. T. Kwong, Shengke Li, Ya-Ting Pan, Jianwen Wei, Lian-Hui Wang, Greta S. P. Mok, Ruibing Wang.  (2021)  Supramolecular nanomedicine derived from cucurbit[7]uril-conjugated nano-graphene oxide for multi-modality cancer therapy.  Biomaterials Science,  (10): (3804-3813).  [PMID:33881050] [10.1039/D1BM00426C]
17. Jiaojiao Fang, Cihui Zhou, Yukai Chen, Liang Fang, Wei Wang, Cheng Zhu, Yaru Ni, Chunhua Lu.  (2019)  Efficient Photocatalysis of Composite Films Based on Plasmon-Enhanced Triplet–Triplet Annihilation.  ACS Applied Materials & Interfaces,      [PMID:31813218] [10.1021/acsami.9b17954]
18. Jiaojiao Fang, Yukai Chen, Wei Wang, Liang Fang, Chunhua Lu, Cheng Zhu, Jiahui Kou, Yaru Ni, Zhongzi Xu.  (2019)  Highly efficient photocatalytic hydrogen generation of g-C3N4-CdS sheets based on plasmon-enhanced triplet–triplet annihilation upconversion.  APPLIED CATALYSIS B-ENVIRONMENTAL,      [PMID:] [10.1016/j.apcatb.2019.117762]
19. Wei Zhu, Li Zhang, Zhe Yang, Pei Liu, Jing Wang, Jinguo Cao, Aiguo Shen, Zushun Xu, Jing Wang.  (2018)  An efficient tumor-inducible nanotheranostics for magnetic resonance imaging and enhanced photodynamic therapy.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2018.10.102]
20. Qian Yang, Chuang Zhao, Jun Zhao, Yong Ye.  (2017)  Synthesis and singlet oxygen activities of near infrared photosensitizers by conjugation with upconversion nanoparticles.  Optical Materials Express,  (3): (913-923).  [PMID:] [10.1364/OME.7.000913]
21. Tian-Yuan Zhang, Bing Huang, Hai-Bin Wu, Jia-He Wu, Li-Ming Li, Yan-Xin Li, Yu-Lan Hu, Min Han, You-Qing Shen, Yasuhiko Tabata, Jian-Qing Gao.  (2015)  Synergistic effects of co-administration of suicide gene expressing mesenchymal stem cells and prodrug-encapsulated liposome on aggressive lung melanoma metastases in mice.  JOURNAL OF CONTROLLED RELEASE,      [PMID:25966361] [10.1016/j.jconrel.2015.05.007]
22. Qingyuan Niu, Kezheng Gao, Wenhui Wu.  (2014)  Cellulose nanofibril based graft conjugated polymer films act as a chemosensor for nitroaromatic.  CARBOHYDRATE POLYMERS,      [PMID:24906727] [10.1016/j.carbpol.2014.03.042]
23. Mingyi Guan, Hui Li, Man Tu, Chenchen Fu, Xiyu Yang, Feng Wang.  (2024)  A novel fluorescent “Off-On” probe based on phenanthro[9,10-d]imidazole conjugated polymers (PIPF) for Cr3+ detection with high selectivity and sensitivity.  SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY,      [PMID:38324948] [10.1016/j.saa.2024.123988]
24. Jiali Peng, Lun Li, Shihuai Deng, Hongyu Zhou, Yanjun Li, Chenye Fu, Long Lin, Yue Yuan, Wei Wei, Guochun Lv, Gang Yang, Xiaohui Lu, Bo Lai.  (2024)  Activation of persulfates on carbon nanotubes for water decontamination: Is the non-radical process consistently considered across different pH levels?.  JOURNAL OF HAZARDOUS MATERIALS,      [PMID:39706015] [10.1016/j.jhazmat.2024.136911]
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