1,10-Phenanthroline Monohydrate - AR, ≥98% , CAS No.5144-89-8

CAS: 5144-89-8 Cat. No.: P104932 Peso molecular: 198.22 Beilstein Registry Number: 4008096 Número EC: 627-114-9
Disponible para pedir
GRADE & PURITY AR ? Analytical Reagent grade — high-purity chemicals meeting strict assay limits for lab analysis. Use when accuracy matters and trace impurities could skew results. ≥98%
Synonyms
J-610049 | s5543 | AMY25697 | 1,10-Phenanthroline hydrate | CCG-266573 | 1,10-PHENANTHROLINE, MONOHYDRATE | 1,10-Phenanthroline monohydrate, ACS reagent, 99% | 1,10-Phenanthroline monohydrate, JIS special grade, >=99.0% | KSX215X00E | 1,10-Phenanthroline
Storage
Room temperature,Argon charged
Shipped In
Normal
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
5g
P104932-5g
4

9,90US$

14,90US$
Guardar 5,00 US$ (33.56%)
10g
P104932-10g
2

12,90US$

19,90US$
Guardar 7,00 US$ (35.18%)
25g
P104932-25g
3

15,90US$

23,90US$
Guardar 8,00 US$ (33.47%)
100g
P104932-100g
3

33,90US$

50,90US$
Guardar 17,00 US$ (33.40%)
500g
P104932-500g
1

120,90US$

181,90US$
Guardar 61,00 US$ (33.53%)
Enter a quantity for the sizes you want to add.
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Why this grade

AR, ≥98% AR for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Room temperature,Argon charged 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 112 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Descripción general

When complexed with copper, it possesses nuclease activity that has been used to study DNA-protein interactions.

Specifications

Sinónimos
J-610049 | s5543 | AMY25697 | 1, 10-Phenanthroline hydrate | CCG-266573 | 1, 10-PHENANTHROLINE, MONOHYDRATE | 1, 10-Phenanthroline monohydrate, ACS reagent, 99% | 1, 10-Phenanthroline monohydrate, JIS special grade, >=99.0% | KSX215X00E | 1, 10-Phenanthroline
Especificaciones y pureza
AR, ≥98%
Mecanismos bioquímicos y fisiológicos
Metalloprotease inhibitor; chelates iron, zinc and other divalent metals. Effective concentration 1-10 mM.
Condiciones de almacenamiento de almacenamiento
Room temperature, Argon charged
Enviado en
Normal
Grado
AR
Pureza
≥98%
Nombres e identificadores
Pubchem Sid488182678
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488182678
Sonrisas canónicasC1=CC2=C(C3=C(C=CC=N3)C=C2)N=C1.O
IUPAC Name1,10-phenanthroline;hydrate
InChIKeyPPQJCISYYXZCAE-UHFFFAOYSA-N
INCHI1S/C12H8N2.H2O/c1-3-9-5-6-10-4-2-8-14-12(10)11(9)13-7-1;/h1-8H;1H2
Isómeros SMILES C1=CC2=C(C3=C(C=CC=N3)C=C2)N=C1.O
WGK Alemania 3
RTECS SF8300000
Número ONU 2811
Grupo de embalaje I
Peso molecular 198.22
Beilstein 4008096
Reaxy-Rn 4008096
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=4008096&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
ClasePhenanthrolines
SubclassNot available
Intermediate Tree Nodes Not available
Direct ParentPhenanthrolines
Alternative Parents Quinolines and derivatives  Pyridines and derivatives  Benzenoids  Heteroaromatic compounds  Azacyclic compounds  Organopnictogen compounds  Organonitrogen compounds  Organic oxides  Hydrocarbon derivatives  
Molecular FrameworkAromatic heteropolycyclic compounds
Substituents 1,10-phenanthroline - Quinoline - Benzenoid - Pyridine - Heteroaromatic compound - Azacycle - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organonitrogen compound - Aromatic heteropolycyclic compound
DescripciónThis compound belongs to the class of organic compounds known as phenanthrolines. These are aromatic polycyclic compounds containing the phenanthroline skeleton, which is a derivative of phenanthrene, and consists of two pyridine rings non-linearly joined by a benzene ring.
External Descriptors Not available
Estructura 3D
Modelo de Estructura Química Interactiva





Mecanismos de acción
Certificados (CoA, COO, BSE/TSE y tabla de análisis)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

60 results found

Lot NumberCertificate TypeFechaArticulo
D2621382Certificate of AnalysisJan 24, 2026 P104932
D2621381Certificate of AnalysisJan 24, 2026 P104932
D2621375Certificate of AnalysisJan 24, 2026 P104932
D2621368Certificate of AnalysisJan 24, 2026 P104932
D2621323Certificate of AnalysisJan 24, 2026 P104932
C2603585Certificate of AnalysisJan 24, 2026 P104932
C2603581Certificate of AnalysisJan 24, 2026 P104932
C2603582Certificate of AnalysisJan 24, 2026 P104932
C2603583Certificate of AnalysisJan 24, 2026 P104932
L2512051Certificate of AnalysisMar 21, 2025 P104932
D2511539Certificate of AnalysisMar 21, 2025 P104932
D2511538Certificate of AnalysisMar 21, 2025 P104932
D2511537Certificate of AnalysisMar 21, 2025 P104932
D2511510Certificate of AnalysisMar 21, 2025 P104932
I2519033Certificate of AnalysisMar 21, 2025 P104932
K2520083Certificate of AnalysisMar 21, 2025 P104932
K2418367Certificate of AnalysisNov 01, 2024 P104932
K2418370Certificate of AnalysisNov 01, 2024 P104932
K2418376Certificate of AnalysisNov 01, 2024 P104932
K2418377Certificate of AnalysisNov 01, 2024 P104932
H2427418Certificate of AnalysisAug 10, 2024 P104932
H2427419Certificate of AnalysisAug 10, 2024 P104932
H2427420Certificate of AnalysisAug 10, 2024 P104932
H2427417Certificate of AnalysisAug 10, 2024 P104932
H2427365Certificate of AnalysisAug 10, 2024 P104932
F2411406Certificate of AnalysisMay 10, 2024 P104932
F2411407Certificate of AnalysisMay 10, 2024 P104932
F2411405Certificate of AnalysisMay 10, 2024 P104932
F2411403Certificate of AnalysisMay 10, 2024 P104932
F2411404Certificate of AnalysisMay 10, 2024 P104932
F2411402Certificate of AnalysisMay 10, 2024 P104932
F2411401Certificate of AnalysisMay 10, 2024 P104932
C2415064Certificate of AnalysisMar 01, 2024 P104932
C2415065Certificate of AnalysisMar 01, 2024 P104932
C2415066Certificate of AnalysisMar 01, 2024 P104932
C2415067Certificate of AnalysisMar 01, 2024 P104932
C2415068Certificate of AnalysisMar 01, 2024 P104932
L2301424Certificate of AnalysisNov 17, 2023 P104932
L2301425Certificate of AnalysisNov 17, 2023 P104932
L2301346Certificate of AnalysisNov 17, 2023 P104932
K2301324Certificate of AnalysisNov 17, 2023 P104932
K2301325Certificate of AnalysisNov 17, 2023 P104932
K2301346Certificate of AnalysisNov 17, 2023 P104932
K2301347Certificate of AnalysisNov 17, 2023 P104932
G2320036Certificate of AnalysisJun 29, 2023 P104932
G2320035Certificate of AnalysisJun 29, 2023 P104932
G2318998Certificate of AnalysisJun 29, 2023 P104932
G23181015Certificate of AnalysisJun 29, 2023 P104932
G23181009Certificate of AnalysisJun 29, 2023 P104932
G23181000Certificate of AnalysisJun 29, 2023 P104932
B2307149Certificate of AnalysisNov 18, 2022 P104932
K22301143Certificate of AnalysisNov 18, 2022 P104932
K22301167Certificate of AnalysisNov 18, 2022 P104932
K22301144Certificate of AnalysisNov 18, 2022 P104932
F2314490Certificate of AnalysisNov 18, 2022 P104932
B2307151Certificate of AnalysisJan 11, 2022 P104932
B2218567Certificate of AnalysisJan 11, 2022 P104932
B2218561Certificate of AnalysisJan 11, 2022 P104932
B2218557Certificate of AnalysisJan 11, 2022 P104932
B2218560Certificate of AnalysisJan 11, 2022 P104932

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Propiedades químicas y físicas
SolubilidadSoluble in water (3 mg/ml), ethanol (25 mg/ml), DMSO (100 mg/ml), acetone, and benzene (70 parts).
SensibilidadMoisture sensitive.
Punto de fusión (°C)97-101°C
Peso molecular198.220 g/mol
XLogP3
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count3
Rotatable Bond Count0
Exact Mass198.079 Da
Monoisotopic Mass198.079 Da
Topological Polar Surface Area26.800 Ų
Heavy Atom Count15
Formal Charge0
Complexity182.000
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 Count2
Preguntas frecuentes y artículos
Citations of This Product
Referencias
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2. Zhengyuan Zhou, Mudassir Habib, Zhiqiang Xu, Guilu Zeng, Rumin Yang, Qian Sui, Shuguang Lyu.  (2023)  Comparative investigation of organic contaminant removal in the synthesized greigite (Fe3S4)- and other iron sulfide-enhanced PDS/Fe(II) systems: Efficiencies, kinetics, and mechanism insights.  SEPARATION AND PURIFICATION TECHNOLOGY,      [PMID:] [10.1016/j.seppur.2023.126059]
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4. Si-Lu Wang, Jie Yu, Jian-Xi Song, Qing-Fan Meng, Zhuo-Rui Zhang, Gui-Quan Jiang.  (2023)  Isolation, purification, structural analysis and in vitro activity of polysaccharides from Amelanchier alnifolia Nutt..  PROCESS BIOCHEMISTRY,      [PMID:] [10.1016/j.procbio.2023.12.002]
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86. Liming Guo, Xin Wan, Jieyuan Liu, Xu Guo, Xiaofang Liu, Jiaxiang Shang, Ronghai Yu, Jianglan Shui.  (2024)  Revealing Distance-Dependent Synergy between MnCo2O4 and Co–N–C in Boosting the Oxygen Reduction Reaction.  ACS Applied Materials & Interfaces,      [PMID:38214267] [10.1021/acsami.3c15627]
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90. Xiao-Shuo Wu, Yi-Wen Wang, Yan-Fen Peng, Shan-Qing Li.  (2025)  Understanding the effect of 1,10-phenanthroline on the photoluminescent properties of mixed-ligand Lead(II) and Zinc(II) coordination polymers.  INORGANICA CHIMICA ACTA,      [PMID:] [10.1016/j.ica.2025.122538]
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101. Yu Kang, Xuetao Xu, Jiankun Lai, Yuepeng Li, Wei Li, Yanqiang Wei, Feilong Zhang, Shutao Wang.  (2025)  Eco-friendly colorful particleboards based on metal-ligand coordination.  Materials Horizons,      [PMID:40237100] [10.1039/D5MH00281H]
102. Mengsi Zhang, Hao Zheng, Xuanqi Zhu, Shuwei Liu, Hao Jin, Yang Chen, Lanlan Wan, Songling Zhang, Hao Zhang.  (2025)  Synchronously Evoking Disulfidptosis and Ferroptosis via Systematical Glucose Deprivation Targeting SLC7A11/GSH/GPX4 Antioxidant Axis.  ACS Nano,      [PMID:40178511] [10.1021/acsnano.5c00730]
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105. Hanyu Yao, Ruixuan Ji, Xiaoyi Song, Bin Yang, Yin Lv, Zhong Wei.  (2025)  pH/GSH Dual-responsive Fe-based MOF drug carrier for ferroptosis-glycolysis synergistic therapy.  NEW JOURNAL OF CHEMISTRY,      [PMID:] [10.1039/D5NJ00944H]
106. Rong-Mei Kong, Na Liang, Shixiao Guo, Xinyue Ge.  (2025)  Dual-emission europium metal-organic framework as fluorescent sensor for sensitive detection of anthrax biomarkers.  MICROCHEMICAL JOURNAL,      [PMID:] [10.1016/j.microc.2025.114322]
107. Jiacheng Zhang, Zixin Xie, Zhangyuan Chen, Xihong Zu, Jiayi Zheng, Wenli Zhang, Dongjie Yang, Xueqing Qiu.  (2025)  Construction of solar-driven electron transfer chain based on FeCl3/TiO2 synergetic mediators for highly efficient conversion of lignin into electricity.  INTERNATIONAL JOURNAL OF HYDROGEN ENERGY,      [PMID:] [10.1016/j.ijhydene.2025.150106]
108. Yusheng Jiang, Xingyu Liu, Teng Li, Hankun Zhang, Lingtao Zeng, Yundi Geng, Hongwei Wu, Changjiang Liu, Hongchao Li, Ding Wang, Yan Li, Chuncheng Yang.  (2025)  Fe-Si-B amorphous magnetic nanoparticles as high-efficiency Fenton-like catalysts for rapid degradation of Rhodamine B.  JOURNAL OF MAGNETISM AND MAGNETIC MATERIALS,      [PMID:] [10.1016/j.jmmm.2025.173561]
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111. Weiyi Zhao, Haotian Zhang, Shuai Yang, Hao Wan, Yao Wei, Tongtong Yang, Xian Wang, Yihui Xu, Wancheng Yu, Zhechen Fan, Yixuan Yin, Lin Lin, Xiaozheng Duan, Junjie Ge, Zheng Jiang.  (2026)  Alleviating the Misalignment of Fe Single Sites Relative to Triple-Phase Interfaces to Achieve High Performance Fuel Cell.  ADVANCED MATERIALS,      [PMID:41631592] [10.1002/adma.202521613]
112. Siyu Yi, Guobin Zhou, Yi Wang, Mengxia Ji, Jinman Yang, Yi Zhang, Pengcheng Yan, Zhao Mo, Zhaolong Wang, Junjie Yuan, Hui Xu, Xiaojie She.  (2026)  Atomic engineering of Cu-N coordination sites for high-performance CO2-to-CH4 electroreduction.  APPLIED CATALYSIS A-GENERAL,      [PMID:] [10.1016/j.apcata.2026.120894]
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