SDS, COA, fiche technique et fiche de spécifications disponibles au téléchargement. COA spécifique au lot accessible via la recherche par numéro de lot.

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Preuve documentaire

Cité dans 71 publications à comité de lecture couvrant la chromatographie, la synthèse organique et les réactions de couplage croisé.

Vue d’ensemble

Le carbazole est une molécule organique hétérocyclique aromatique. Il interagit principalement avec l'ADN et l'endommage. Ces événements empêchent la synthèse de nouveaux ADN ou ARN. Les dérivés du carbazole sont impliqués dans des activités antimicrobiennes, antitumorales, antiépileptiques, antihistaminiques, antioxydantes, anti-inflammatoires, antidiarrhéiques, analgésiques, neuroprotectrices et de suppression de la lipase pancréatique.
Le carbazole a été utilisé dans le dosage de l'acide uronique

Spécifications

Synonymes

Spécifications et pureté

≥96%

Conditions de stockage de stockage

Room temperature

Expédié en

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Pureté

≥96%

Noms et identifiants

Pubchem Sid

488180177

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/488180177

Sourires canoniques

C1=CC=C2C(=C1)C3=CC=CC=C3N2

IUPAC Name

9H-carbazole

InChIKey

UJOBWOGCFQCDNV-UHFFFAOYSA-N

INCHI

1S/C12H9N/c1-3-7-11-9(5-1)10-6-2-4-8-12(10)13-11/h1-8,13H

Isomères SMILES

C1=CC=C2C(=C1)C3=CC=CC=C3N2

WGK Allemagne

RTECS

FE3150000

Numéro ONU

3077

Groupe d'emballage

III

Poids moléculaire

167.21

Beilstein

3956

Reaxy-Rn

3956

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=3956&ln=

Documentation

📋 Fiche de données de sécurité (FDS)

Document complet couvrant les dangers, la manipulation, le stockage et la conformité réglementaire.

<<<<<<< HEAD Télécharger la SDS → ======= Télécharger la SDS → >>>>>>> release248-p3

✅ Certificat d'analyse (COA)

Données qualité spécifiques au lot. Saisissez votre numéro de lot pour récupérer le COA exact.

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📊 Fiche technique

Résumé de référence rapide des spécifications et applications du produit.

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🔬 Fiche de spécifications

Attributs de qualité complets et critères d'acceptation pour cette qualité.

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Données avancées

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Organoheterocyclic compounds
  - Classe Indoles and derivatives
    - Subclass Carbazoles

Kingdom	Organic compounds
Superclass	Organoheterocyclic compounds
Classe	Indoles and derivatives
Subclass	Carbazoles
Intermediate Tree Nodes	Not available
Direct Parent	Carbazoles
Alternative Parents	Indoles Benzenoids Pyrroles Heteroaromatic compounds Azacyclic compounds Organopnictogen compounds Organonitrogen compounds Hydrocarbon derivatives
Molecular Framework	Aromatic heteropolycyclic compounds
Substituents	Carbazole - Indole - Benzenoid - Heteroaromatic compound - Pyrrole - Azacycle - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Organonitrogen compound - Aromatic heteropolycyclic compound
Description	This compound belongs to the class of organic compounds known as carbazoles. These are compounds containing a three ring system containing a pyrrole ring fused on either side to a benzene ring.
External Descriptors	a carbazole
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. DOI: 10.1186/s13321-016-0174-y

Structure 3D

Cibles associées (humaines)

AR Tclin Androgen Receptor (11781 Activities)

Discover Target: AR

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

TYR Tclin Tyrosinase (717 Activities)

Discover Target: TYR

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

PTH1R Tclin Parathyroid hormone receptor (47172 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

ALDH1A1 Tchem Aldehyde dehydrogenase 1A1 (77053 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

U-937 (7138 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

KIF11 Tchem Kinesin-like protein 1 (1720 Activities)

Discover Target: KIF11

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

HSD17B10 Tchem Endoplasmic reticulum-associated amyloid beta-peptide-binding protein (20669 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Cibles associées (non humaines)

Staphylococcus aureus (210822 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Bovine viral diarrhea virus 1 (1277 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Nfe2l2 Nuclear factor erythroid 2-related factor 2 (214 Activities)

Discover Target: Nfe2l2

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Rorc Nuclear receptor ROR-gamma (89407 Activities)

Discover Target: Rorc

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

clpP ATP-dependent Clp protease proteolytic subunit (245 Activities)

Discover Target: clpP

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Mécanismes d'action

Certificats (CoA, COO, BSE/TSE et tableau d'analyse)

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.

27 results found

Lot Number	Certificate Type	Date	Article
E2626330	Certificate of Analysis	Jun 06, 2026	C104875
E2626328	Certificate of Analysis	Jun 06, 2026	C104875
E2626321	Certificate of Analysis	Jun 06, 2026	C104875
F2528101	Certificate of Analysis	Jul 05, 2025	C104875
F2530069	Certificate of Analysis	Jul 02, 2025	C104875
F2530068	Certificate of Analysis	Jul 02, 2025	C104875
F2530006	Certificate of Analysis	Jul 02, 2025	C104875
D2621034	Certificate of Analysis	Jul 02, 2025	C104875
B2505091	Certificate of Analysis	Feb 08, 2025	C104875
D2115186	Certificate of Analysis	Jan 10, 2025	C104875
D2115188	Certificate of Analysis	Jan 10, 2025	C104875
D2115182	Certificate of Analysis	Jan 10, 2025	C104875
H2322042	Certificate of Analysis	Aug 25, 2023	C104875
B2306864	Certificate of Analysis	Feb 09, 2023	C104875
C23201125	Certificate of Analysis	Sep 17, 2022	C104875
F23051075	Certificate of Analysis	Sep 17, 2022	C104875
I2214366	Certificate of Analysis	Sep 17, 2022	C104875
I2214367	Certificate of Analysis	Sep 17, 2022	C104875
I2214368	Certificate of Analysis	Sep 17, 2022	C104875
I2214369	Certificate of Analysis	Sep 17, 2022	C104875
L2404065	Certificate of Analysis	Jan 21, 2022	C104875
B2306861	Certificate of Analysis	Jan 21, 2022	C104875
A2212198	Certificate of Analysis	Jan 21, 2022	C104875
A2212195	Certificate of Analysis	Jan 21, 2022	C104875
A2212194	Certificate of Analysis	Jan 21, 2022	C104875
A2212193	Certificate of Analysis	Jan 18, 2022	C104875
A2418042	Certificate of Analysis	Apr 22, 2021	C104875

Propriétés chimiques et physiques

Solubilité	It is insoluble in water;Solubility in hot EtOH:almost transparency
Point d'éclair (°F)	428℉
Point d'éclair (°C)	220°C
Point d'ébullition (°C)	355°C
Point de fusion (°C)	245°C
Poids moléculaire	167.210 g/mol
XLogP3	3.700
Hydrogen Bond Donor Count	1
Hydrogen Bond Acceptor Count	0
Rotatable Bond Count	0
Exact Mass	167.073 Da
Monoisotopic Mass	167.073 Da
Topological Polar Surface Area	15.800 Å²
Heavy Atom Count	13
Formal Charge	0
Complexity	170.000
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	1

FAQ et articles

Light-Emitting Polymers (LEPs): A Practical Panorama - A Core PL/EL Mechanistic Framework, Material Family Map, and Structural “Design Knobs” (including Product Tables 1–4 and a selection guide)

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

Light-Emitting Polymers LEPs

Why Carbazole Is So Common in OLEDs: Managing Charge Carriers, Excitons, and Film Morphology with a Building-Block Mindset (with Selection Guide and Tables 1–3)

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

OLED

Pyrrole Research Reagent Selection Roadmap: Structure—Reactive Sites—Application Throughline and Reagent Classification Guide (Tables 1–4)

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

Pyrrole five-membered aromatic

Citations of This Product

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📚 Citations par application

Extraction & workup solvent21

Organic synthesis — reaction medium42

Polymer synthesis & polymerization10

Other applications33

Electrochemistry & battery electrolyte12

Spectroscopy sample preparation3

Chromatography (HPLC / GC / TLC)5

Cross-coupling reactions1

Controlled-release & nanoparticle carrier1

Topical & ophthalmic formulation1

Drug / compound screening1

Industrial & non-pharma application1

Crystallization & recrystallization2

Voir les 71 citations →

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Carbazole - ≥96% , CAS No.86-74-8

Stockage & expédition

Documents qualité

Preuve documentaire

Vue d’ensemble

Spécifications

Documentation

📋 Fiche de données de sécurité (FDS)

✅ Certificat d'analyse (COA)

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