2,3-Diaminophenazine - ≥90% , CAS No.655-86-7

CAS: 655-86-7 Cat. No.: D139150 Peso molecular: 210.23 Número EC: 211-512-0
Disponible para pedir
GRADE & PURITY ≥90%
Synonyms
AC-31133 | UNII-0B20H27U1Y | Z56757698 | 2,3-Phenazinediamine | PS-5430 | VZPGINJWPPHRLS-UHFFFAOYSA-N | A847172 | (3-aminophenazin-2-yl)amine | 2,3-Diaminophenazine, 90% | Phenazine, 2,3-diamino- | BCP08073 | NSC26432 | AKOS000112882 | BRN 0014422 | FT-06
Storage
Argon charged,Room temperature
Shipped In
Normal
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
1g
D139150-1g
9

21,90US$

32,90US$
Guardar 11,00 US$ (33.43%)
5g
D139150-5g
4

69,90US$

104,90US$
Guardar 35,00 US$ (33.37%)
25g
D139150-25g
1-2 wks(?)
Item is derived from our semi-finished stock and is processed in 1-2 weeks.

261,90US$

392,90US$
Guardar 131,00 US$ (33.34%)
Enter a quantity for the sizes you want to add.
🧪

Why this grade

≥90% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

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

📋

Quality documents

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

📚

Literature proof

Cited in 13 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Sinónimos
AC-31133 | UNII-0B20H27U1Y | Z56757698 | 2, 3-Phenazinediamine | PS-5430 | VZPGINJWPPHRLS-UHFFFAOYSA-N | A847172 | (3-aminophenazin-2-yl)amine | 2, 3-Diaminophenazine, 90% | Phenazine, 2, 3-diamino- | BCP08073 | NSC26432 | AKOS000112882 | BRN 0014422 | FT-06
Especificaciones y pureza
≥90%
Condiciones de almacenamiento de almacenamiento
Argon charged, Room temperature
Enviado en
Normal
Pureza
≥90%
Nombres e identificadores
Pubchem Sid488189689
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488189689
Sonrisas canónicasC1=CC=C2C(=C1)N=C3C=C(C(=CC3=N2)N)N
IUPAC Namephenazine-2,3-diamine
InChIKeyVZPGINJWPPHRLS-UHFFFAOYSA-N
INCHI1S/C12H10N4/c13-7-5-11-12(6-8(7)14)16-10-4-2-1-3-9(10)15-11/h1-6H,13-14H2
Isómeros SMILES C1=CC=C2C(=C1)N=C3C=C(C(=CC3=N2)N)N
WGK Alemania 3
RTECS SG1577650
Peso molecular 210.23
Reaxy-Rn 14422
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=14422&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
ClaseDiazanaphthalenes
SubclassBenzodiazines
Intermediate Tree Nodes Quinoxalines
Direct ParentPhenazines and derivatives
Alternative Parents Pyrazines  Benzenoids  Heteroaromatic compounds  Azacyclic compounds  Primary amines  Organopnictogen compounds  Hydrocarbon derivatives  
Molecular FrameworkAromatic heteropolycyclic compounds
Substituents Phenazine - Benzenoid - Pyrazine - Heteroaromatic compound - Azacycle - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Primary amine - Organonitrogen compound - Amine - Aromatic heteropolycyclic compound
DescripciónThis compound belongs to the class of organic compounds known as phenazines and derivatives. These are polycyclic aromatic compounds containing a phenazine moiety, which is a linear tricyclic system that consists of a two benzene rings joined by a pyrazine ring.
External Descriptors Not available
Estructura 3D
Modelo de Estructura Química Interactiva





Objetivos asociados (humanos)
POLB Tchem DNA polymerase beta (23632 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PLK1 Tchem Serine/threonine-protein kinase PLK1 (28605 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
GLP1R Tclin Glucagon-like peptide 1 receptor (111429 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PIN1 Tchem Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 (36611 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Huh-7 (12904 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
A549 (127892 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
POLI Tchem DNA polymerase iota (116820 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
EHMT2 Tchem Histone-lysine N-methyltransferase, H3 lysine-9 specific 3 (93046 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
TSG101 Tbio Tumor susceptibility gene 101 protein (2874 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
TDP1 Tchem Tyrosyl-DNA phosphodiesterase 1 (345557 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
L3MBTL1 Tchem Lethal(3)malignant brain tumor-like protein 1 (14536 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
USP2 Tbio Ubiquitin carboxyl-terminal hydrolase 2 (8818 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
NPC1 Tchem Niemann-Pick C1 protein (18985 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
KMT2A Tchem Histone-lysine N-methyltransferase MLL (17327 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ATAD5 Tbio ATPase family AAA domain-containing protein 5 (122566 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
BAZ2B Tchem Bromodomain adjacent to zinc finger domain protein 2B (56204 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
APAF1 Tchem Apoptotic protease-activating factor 1 (1188 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MEN1 Tchem Menin/Histone-lysine N-methyltransferase MLL (48157 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CACNA1B Tclin Voltage-gated N-type calcium channel alpha-1B subunit/Amyloid beta A4 precursor protein-binding family A member 1 (925 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
WRN Tbio Werner syndrome ATP-dependent helicase (8824 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Objetivos asociados (no humanos)
Plasmodium falciparum (966862 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Luciferin 4-monooxygenase (66902 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mapt Microtubule-associated protein tau (6 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
fba Putative fructose-1,6-bisphosphate aldolase (15559 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ffp 4'-phosphopantetheinyl transferase ffp (24982 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
rev Protein Rev (94 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
gld-1 Female germline-specific tumor suppressor gld-1 (77 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
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.

18 results found

Lot NumberCertificate TypeFechaArticulo
G2522661Certificate of AnalysisJun 24, 2025 D139150
G2522659Certificate of AnalysisJun 24, 2025 D139150
G2516374Certificate of AnalysisJun 24, 2025 D139150
C2603069Certificate of AnalysisJun 24, 2025 D139150
L2419054Certificate of AnalysisDec 16, 2024 D139150
B2328617Certificate of AnalysisDec 16, 2024 D139150
B2328618Certificate of AnalysisDec 13, 2024 D139150
B2328615Certificate of AnalysisDec 13, 2024 D139150
B2328614Certificate of AnalysisDec 13, 2024 D139150
H2223229Certificate of AnalysisJun 15, 2024 D139150
H2223230Certificate of AnalysisJun 15, 2024 D139150
H2402206Certificate of AnalysisApr 15, 2024 D139150
B2328619Certificate of AnalysisDec 13, 2022 D139150
G2423029Certificate of AnalysisDec 13, 2022 D139150
B2328616Certificate of AnalysisDec 13, 2022 D139150
H2409082Certificate of AnalysisDec 13, 2022 D139150
L2406294Certificate of AnalysisDec 13, 2022 D139150
H2223228Certificate of AnalysisAug 11, 2022 D139150

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Propiedades químicas y físicas
SensibilidadAir sensitive
Punto de fusión (°C)>300 °C
Peso molecular210.230 g/mol
XLogP31.300
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count4
Rotatable Bond Count0
Exact Mass210.091 Da
Monoisotopic Mass210.091 Da
Topological Polar Surface Area77.800 Ų
Heavy Atom Count16
Formal Charge0
Complexity231.000
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. Lu Sun, Lin-Ge Chen, Hai-Bo Wang.  (2023)  Fenton-like reaction triggered chemical redox-cycling signal amplification for ultrasensitive fluorometric detection of H2O2 and glucose.  ANALYST,  149  (2): (546-552).  [PMID:38088105] [10.1039/D3AN01682J]
2. Hongcan Sun, Pengfei Xia, Haibao Shao, Rong Zhang, Changgui Lu, Shuhong Xu, Chunlei Wang.  (2023)  Heating-free synthesis of red emissive carbon dots through separated processes of polymerization and carbonization.  JOURNAL OF COLLOID AND INTERFACE SCIENCE,      [PMID:37235938] [10.1016/j.jcis.2023.05.120]
3. Xiaojie Chang, Guizhi Zhao, Chang Liu, Xueshi Wang, Ahmed Mohammed Ali Abdulkhaleq, Jie Zhang, Xibin Zhou.  (2022)  One-step microwave synthesis of red-emissive carbon dots for cell imaging in extreme acidity and light emitting diodes.  RSC Advances,  12  (43): (28021-28033).  [PMID:36320228] [10.1039/D2RA04026C]
4. Zhi-Ang Liu, Ya-Nan Zuo, Yinghui Xia, Jing Sun, Shuyun Zhu.  (2022)  Enhanced detection of ascorbic acid with cascaded fluorescence recovery of a dual-nanoquencher system.  Analytical Methods,  14  (37): (3632-3637).  [PMID:36052693] [10.1039/D2AY01019D]
5. Xiaoyan Sun, Yuxin Guo, Ruizhi Wen, Hongchang Li.  (2021)  A highly sensitive and selective ratiometric sensing platform based on 7-amino-4-methylcoumarin for naked-eye visual fluorescence sensing of Cu2+.  SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY,      [PMID:34836812] [10.1016/j.saa.2021.120627]
6. Yunjie Zhou, Yue Sun, Huibo Wang, Cheng Zhu, Jin Gao, Dan Wu, Hui Huang, Yang Liu, Zhenhui Kang.  (2018)  A nitrogen and boron co-doped metal-free carbon electrocatalyst for an efficient oxygen reduction reaction.  Inorganic Chemistry Frontiers,  (11): (2985-2991).  [PMID:] [10.1039/C8QI00853A]
7. Longyu Zhang, Weijun Peng, Wei Wang, Yijun Cao, Mengyao Qi, Yukun Huang.  (2024)  A green method for selective separation of molybdenite and pyrite via electrochemical oxidation pretreatment-flotation and its mechanism.  COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS,      [PMID:] [10.1016/j.colsurfa.2024.133508]
8. Shiyuan Liu, Jiacong Wu, Xinnan Ma, Lei Wang, Juan Han, Yun Wang.  (2024)  A novel photo-enzyme platform based on non-metallic modified carbon nitride for removal of bisphenol A in water.  INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES,      [PMID:38408583] [10.1016/j.ijbiomac.2024.130402]
9. Liyuan Zhang, Ruiting Zhang, Jinchen Wang, Jiayu Chen, Runzhong Yu.  (2024)  A ratiometric fluorescence sensing system for rapid detection of glyphosate in miscellaneous beans.  JOURNAL OF FOOD COMPOSITION AND ANALYSIS,      [PMID:] [10.1016/j.jfca.2024.106457]
10. Qin Hu, Qiuyan Mao, Yikun Cui, Shiyun Gong, Lixia Xiao, Xiaojuan Gong, Tianzhu Guan, Zhen-quan Yang.  (2024)  Carbon dots-based fluorescence microspheres for ultrasensitive detection of malachite green in fish samples.  JOURNAL OF FOOD COMPOSITION AND ANALYSIS,      [PMID:] [10.1016/j.jfca.2024.106497]
11. Jian Liu, Junbo Li, Yan Huang, Tong Li, Cheng Xu, Zhengyu Tao, Wei Ji, Xin Huang.  (2025)  Liquid-to-gel transitions of phase-separated coacervate microdroplets enabled by endogenous enzymatic catalysis.  JOURNAL OF COLLOID AND INTERFACE SCIENCE,      [PMID:40184654] [10.1016/j.jcis.2025.137486]
12. Feng Zhang, Mengke Wang, Lili Zhang, Xingguang Su.  (2019)  Ratiometric fluorescence system for pH sensing and urea detection based on MoS2 quantum dots and 2, 3-diaminophenazine.  ANALYTICA CHIMICA ACTA,      [PMID:31307710] [10.1016/j.aca.2019.06.001]
13. Xin Wang, Huiru Sheng, Pengyue Wang, Xiang Li, Xinyi Liang, Qingyu Xu, Chunpeng Jiao, Jingbin Zeng.  (2025)  Nanozyme-driven ratiometric monitoring of uranyl ions in aquatic systems: Mechanisms, environmental validation, and bioaccumulation assessment.  JOURNAL OF HAZARDOUS MATERIALS,      [PMID:41401529] [10.1016/j.jhazmat.2025.140809]
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