Carbazole

Name: Carbazole
Brand: SIGMA
Price: 263 PLN

VETRANAL^®, analytical standard

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250 MG

PLN 263.00

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About This Item

Empirical Formula (Hill Notation):

C₁₂H₉N

CAS Number:

86-74-8

Molecular Weight:

167.21

UNSPSC Code:

41116107

NACRES:

NA.24

PubChem Substance ID:

329756603

EC Number:

201-696-0

Beilstein/REAXYS Number:

3956

MDL number:

MFCD00004960

Key Documents

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Product Name

Carbazole, VETRANAL^®, analytical standard

InChI key

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

SMILES string

c1ccc2c(c1)[nH]c3ccccc23

grade

analytical standard

vapor pressure

400 mmHg ( 323 °C)

product line

VETRANAL^®

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

bp

355 °C (lit.)

mp

243-246 °C (lit.)

application(s)

clinical
environmental

format

neat

Quality Level

100

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Show Differences

1 of 4

This Item	C5132	8.20255	PHR1564
Supelco 46100 Carbazole	Sigma-Aldrich C5132 Carbazole	Sigma-Aldrich 8.20255 Carbazole	Supelco PHR1564 Carprofen Related Compound A
technique(s) HPLC: suitable, gas chromatography (GC): suitable	technique(s) titration: suitable	technique(s) -	technique(s) HPLC: suitable, gas chromatography (GC): suitable
application(s) clinical environmental	application(s) diagnostic assay manufacturing hematology histology	application(s) -	application(s) pharmaceutical (small molecule)
format neat	format -	format -	format neat
Quality Level 100	Quality Level 200	Quality Level 200	Quality Level 300
grade analytical standard	grade -	grade -	grade certified reference material, pharmaceutical secondary standard
shelf life limited shelf life, expiry date on the label	shelf life -	shelf life -	shelf life -

Legal Information

VETRANAL is a registered trademark of Merck KGaA, Darmstadt, Germany

pictograms

GHS08

signalword

Warning

hcodes

H341,H351,H413

pcodes

P202 - P273 - P280 - P308 + P313 - P405 - P501

Hazard Classifications

Aquatic Chronic 4 - Carc. 2 - Muta. 2

Storage Class

11 - Combustible Solids

wgk

WGK 2

flash_point_f

428.0 °F - closed cup

flash_point_c

220.0 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges

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Certificates of Analysis (COA)

Lot/Batch Number

BCCL7015

BCCD7871

BCBS8735

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Structural insight into the substrate- and dioxygen-binding manner in the catalytic cycle of rieske nonheme iron oxygenase system, carbazole 1,9a-dioxygenase.

Yuji Ashikawa et al.

BMC structural biology, 12, 15-15 (2012-06-26)

Dihydroxylation of tandemly linked aromatic carbons in a cis-configuration, catalyzed by multicomponent oxygenase systems known as Rieske nonheme iron oxygenase systems (ROs), often constitute the initial step of aerobic degradation pathways for various aromatic compounds. Because such RO reactions inherently

Combined ultrasound/ozone degradation of carbazole in APG1214 surfactant solution.

Guodong Ji et al.

Journal of hazardous materials, 225-226, 1-7 (2012-05-23)

We examined the effects of power and treatment time on the ultrasonically enhanced ozonation of carbazole dissolved in APG(1214) surfactant solutions, including an analysis of the mechanism of OH radical formation, the zeta potential of the colloidal suspension, the influence

New host material for high-performance blue phosphorescent organic electroluminescent devices.

Jong-Kwan Bin et al.

Advanced materials (Deerfield Beach, Fla.), 24(21), 2911-2915 (2012-05-03)

A new carbazole derivative with two carbazole moieties on the C3 and C6 positions of carbazole and triphenylsilane directly linked to the N of carbazole is successfully used as a highly efficient blue phosphorescent host in an organic light-emitting diode

Application of a Raney-cobalt-mediated tandem reductive cyclization protocol to total syntheses of the Aspidosperma alkaloids (±)-limaspermidine and (±)-1-acetylaspidoalbidine.

Shen H Tan et al.

Organic letters, 14(22), 5621-5623 (2012-10-31)

The racemic modification of the Aspidosperma alkaloid limaspermidine (1) has been prepared in ten steps including one involving a Raney-cobalt-mediated tandem reductive cyclization of nitrile 8 to give the tetracyclic system 9b. Compound (±)-1 has been converted over two steps

Bicarbazoles: systematic structure-property investigations on a series of conjugated carbazole dimers.

Shin-ichiro Kato et al.

The Journal of organic chemistry, 77(20), 9120-9133 (2012-09-19)

A large series of conjugated carbazole dimers, namely bicarbazoles 1-12, were synthesized by Suzuki-Miyaura, Sonogashira, Hay, and McMurry coupling reactions. In 1-12, the two carbazole moieties are linked at the 1-, 2-, or 3-position directly or via an acetylenic or

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