APF - ≥95%, ~5mM in dimethyl formamide , CAS No.359010-70-1

CAS: 359010-70-1 Cat. No.: A356800 Peso molecular: 423.42 Número EC: 962-224-3
Disponible para pedir
GRADE & PURITY ≥95% ~5mM in dimethyl formamide
Synonyms
2-[3-(4-aminophenoxy)-6-oxoxanthen-9-yl]benzoic acid | DTXSID40469879 | 2-(6-(4-Aminophenoxy)-3-oxo-3H-xanthen-9-yl)benzoic acid | SCHEMBL1968894 | 2-[6-(4-AMINOPHENOXY)-3-OXO-3H-XANTHEN-9-YL]BENZOIC ACID | 2-[6-(4-Aminophenoxy)-3-oxo-3H-xanthen-9-yl]-ben
Storage
Store at 2-8°C
Shipped In
Wet ice
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Size
Estado
Price
Qty
1mg
A356800-1mg
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1.185,90US$
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Why this grade

≥95%, ~5mM in dimethyl formamide for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Store at 2-8°C Ships Wet ice 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 10 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Descripción general

APF is a fluorescent reagent (λ|Ex|max|: 490nm; λ|Em|max|: 515nm) used in the detection of highly reactive oxygen species (hROS). Immediately reacts with hROS such as hydroxyl radical, peroxynitrite and hypochlorite, and the fluorescence intensity greatly increases. When using APF together with HPF, it also allows for specific detection of hypochlorite (|-|OCl) to elucidate reliable roles of|-|OCl in biological systems such as netrophils. Peroxynitrite can also be detected in distinction from nitric oxide and superoxide since APF does not react with nitric oxide, superoxide and hydrogen peroxide. APF is resistant to light-induced autooxidation

Specifications

Sinónimos
2-[3-(4-aminophenoxy)-6-oxoxanthen-9-yl]benzoic acid | DTXSID40469879 | 2-(6-(4-Aminophenoxy)-3-oxo-3H-xanthen-9-yl)benzoic acid | SCHEMBL1968894 | 2-[6-(4-AMINOPHENOXY)-3-OXO-3H-XANTHEN-9-YL]BENZOIC ACID | 2-[6-(4-Aminophenoxy)-3-oxo-3H-xanthen-9-yl]-ben
Especificaciones y pureza
≥95%, ~5mM in dimethyl formamide
Condiciones de almacenamiento de almacenamiento
Store at 2-8°C
Enviado en
Wet ice
Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.
Nota
Prepare 500-5'000-fold dilution (~10-1µM) in phosphate buffer (0.1M phosphate, pH 7.4) immediately before use. BSA, phenol red and amines may affect the fluorescence and must be used with caution. Do not store the dilutions.", '
Pureza
≥95%
Propiedades del producto
Rangos de excitación y emisiónλex 490 nm, λem 515 nm
Nombres e identificadores
Sonrisas canónicasC1=CC=C(C(=C1)C2=C3C=CC(=O)C=C3OC4=C2C=CC(=C4)OC5=CC=C(C=C5)N)C(=O)O
IUPAC Name2-[3-(4-aminophenoxy)-6-oxoxanthen-9-yl]benzoic acid
InChIKeyGIERQYKZWFLVGR-UHFFFAOYSA-N
INCHI1S/C26H17NO5/c27-15-5-8-17(9-6-15)31-18-10-12-22-24(14-18)32-23-13-16(28)7-11-21(23)25(22)19-3-1-2-4-20(19)26(29)30/h1-14H,27H2,(H,29,30)
Isómeros SMILES C1=CC=C(C(=C1)C2=C3C=CC(=O)C=C3OC4=C2C=CC(=C4)OC5=CC=C(C=C5)N)C(=O)O
Peso molecular 423.42
Reaxy-Rn 29522143
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=29522143&ln=

Documentation

📋 Safety Data Sheet (SDS)

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

Download SDS →

✅ Certificate of Analysis (COA)

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

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganoheterocyclic compounds
ClaseBenzopyrans
Subclass1-benzopyrans
Intermediate Tree Nodes Dibenzopyrans
Direct ParentXanthenes
Alternative Parents Diarylethers  Benzoic acids  Phenoxy compounds  Phenol ethers  Aniline and substituted anilines  Benzoyl derivatives  Primary aromatic amines  Heteroaromatic compounds  Amino acids  Cyclic ketones  Oxacyclic compounds  Monocarboxylic acids and derivatives  Carboxylic acids  Organopnictogen compounds  Organic oxides  Hydrocarbon derivatives  
Molecular FrameworkAromatic heteropolycyclic compounds
Substituents Xanthene - Diaryl ether - Benzoic acid or derivatives - Benzoic acid - Phenoxy compound - Benzoyl - Aniline or substituted anilines - Phenol ether - Monocyclic benzene moiety - Benzenoid - Primary aromatic amine - Heteroaromatic compound - Amino acid or derivatives - Amino acid - Cyclic ketone - Carboxylic acid derivative - Carboxylic acid - Oxacycle - Ether - Monocarboxylic acid or derivatives - Organic nitrogen compound - Amine - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Organopnictogen compound - Organonitrogen compound - Organooxygen compound - Primary amine - Aromatic heteropolycyclic compound
DescripciónThis compound belongs to the class of organic compounds known as xanthenes. These are polycyclic aromatic compounds containing a xanthene moiety, which consists of two benzene rings joined to each other by a pyran ring.
External Descriptors Not available
Estructura 3D
Modelo de Estructura Química Interactiva





Certificados (CoA, COO, BSE/TSE y tabla de análisis)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
Propiedades químicas y físicas
SolubilidadInsoluble in water.
Índice de refracciónn20D1.75 (Predicted)
Punto de ebullición (°C)153° C
Peso molecular423.400 g/mol
XLogP33.600
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count6
Rotatable Bond Count4
Exact Mass423.111 Da
Monoisotopic Mass423.111 Da
Topological Polar Surface Area98.900 Ų
Heavy Atom Count32
Formal Charge0
Complexity850.000
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
Preguntas frecuentes y artículos
Citations of This Product
Referencias
1. Guoting Su, Hui Xu, FangFang Zhou, Xiyu Gong, Songwen Tan, Yongju He.  (2023)  Boosting Reactive Oxygen Species Generation with a Dual-Catalytic Nanomedicine for Enhanced Tumor Nanocatalytic Therapy.  ACS Applied Materials & Interfaces,      [PMID:38095444] [10.1021/acsami.3c13882]
2. Xingyu Fan, Xiyu Gong, Fangfang Zhou, Botao Chen, Songwen Tan, Hui Xu, Anqiang Pan, Shuquan Liang, Yongju He.  (2022)  Mesoporous peroxidase nanozyme for synergistic chemodynamic therapy and chemotherapy.  COLLOIDS AND SURFACES B-BIOINTERFACES,      [PMID:35653958] [10.1016/j.colsurfb.2022.112603]
3. Linjie Shao, Taishun Hu, Xingyu Fan, Xiaozan Wu, Fangfang Zhou, Botao Chen, Songwen Tan, Hui Xu, Anqiang Pan, Shuquan Liang, Yongju He.  (2022)  Intelligent Nanoplatform with Multi Therapeutic Modalities for Synergistic Cancer Therapy.  ACS Applied Materials & Interfaces,      [PMID:35286061] [10.1021/acsami.2c01913]
4. Li Cong, Lai Chaoyang, Qiu Qiujun, Luo Xiang, Hu Ling, Zheng Huangliang, Lu Yi, Liu Min, Zhang Hongxia, Liu Xinrong, Deng Yihui, Song Yanzhi.  (2019)  Dual-Ligand Modification of PEGylated Liposomes Used for Targeted Doxorubicin Delivery to Enhance Anticancer Efficacy.  AAPS PHARMSCITECH,  20  (5): (1-13).  [PMID:31093777] [10.1208/s12249-019-1385-0]
5. Chaoyang Lai, Cong Li, Mengyang Liu, Qiujun Qiu, Xiang Luo, Xinrong Liu, Ling Hu, Yihui Deng, Yanzhi Song.  (2018)  Effect of Kupffer cells depletion on ABC phenomenon induced by Kupffer cells-targeted liposomes.  Asian Journal of Pharmaceutical Sciences,      [PMID:32104474] [10.1016/j.ajps.2018.07.004]
6. Chaoyang Lai, Cong Li, Xiang Luo, Mengyang Liu, Xinrong Liu, Ling Hu, Le Kang, Qiujun Qiu, Yihui Deng, Yanzhi Song.  (2018)  Use of Dual-Ligand Modification in Kupffer Cell-Targeted Liposomes To Examine the Contribution of Kupffer Cells to Accelerated Blood Clearance Phenomenon.  MOLECULAR PHARMACEUTICS,      [PMID:29768009] [10.1021/acs.molpharmaceut.8b00042]
7. Yongju He, Xiangjie Tian, Meiru Zhang, Hui Xu, Xiyu Gong, Binbin Yang, Fangfang Zhou.  (2024)  Fenton-like nanoparticles capable of H2O2 self-supply and glutathione consumption for chemodynamic and chemotherapy of cancer.  Biomaterials Science,      [PMID:39267609] [10.1039/D4BM00930D]
8. Xiangjie Tian, Hui Xu, FangFang Zhou, Xiyu Gong, Songwen Tan, Yongju He.  (2024)  An Intelligent Cupreous Nanoplatform with Self-Supplied H2O2 and Cu2+/Cu+ Conversion to Boost Cuproptosis and Chemodynamic Combined Therapy.  CHEMISTRY OF MATERIALS,      [PMID:] [10.1021/acs.chemmater.3c02323]
9. Meiru Zhang, Hui Xu, Xiaozan Wu, Botao Chen, Xiyu Gong, Yongju He.  (2025)  Engineering Dual-Responsive Nanoplatform Achieves Copper Metabolism Disruption and Glutathione Consumption to Provoke Cuproptosis/Ferroptosis/Apoptosis for Cancer Therapy.  ACS Applied Materials & Interfaces,      [PMID:40134095] [10.1021/acsami.4c22546]
10. Jieming Zhang, Fangfang Zhou, Xin Du, Meiru Zhang, Suxiao Li, Songtao Niu, Qungang Chang, Yongju He.  (2025)  Tumor-Specific Activatable Nanopaltform Achieves Oxidative Stress Amplification and Reversal of Cisplatin Resistance to Provoke Enhanced Ferroptosis–Apoptosis Cancer Therapy.  MOLECULAR PHARMACEUTICS,      [PMID:40500911] [10.1021/acs.molpharmaceut.5c00406]
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