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Merck

C5132

Carbazole

≥95% purity (GC), powder

Synonym(s):

Dibenzopyrrole; Diphenylenimine

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100 G

PLN 385.00

250 G

PLN 749.00

500 G

PLN 1,380.00

PLN 385.00

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About This Item

Empirical Formula (Hill Notation):
C12H9N
CAS Number:
86-74-8
Molecular Weight:
167.21
NACRES:
NA.47
PubChem Substance ID:
24892756
UNSPSC Code:
12171500
EC Number:
201-696-0
MDL number:
MFCD00004960
Beilstein/REAXYS Number:
3956

Key Documents

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Product Name

Carbazole, ≥95% (GC)

InChI

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

InChI key

UJOBWOGCFQCDNV-UHFFFAOYSA-N

SMILES string

c1ccc2c(c1)[nH]c3ccccc23

vapor pressure

400 mmHg ( 323 °C)

assay

≥95% (GC)

form

powder

technique(s)

titration: suitable

color

white to tan

bp

355 °C (lit.)

mp

243-246 °C (lit.)

solubility

acetone: 50 mg/mL

density

1.1 g/cm3 at 18 °C

application(s)

diagnostic assay manufacturing
hematology
histology

storage temp.

room temp

Quality Level

200

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1 of 4

This Item
461008.20255PHR1564
Carbazole ≥95% (GC)

Sigma-Aldrich

C5132

Carbazole

Carbazole VETRANAL®, analytical standard

Supelco

46100

Carbazole

Carbazole for synthesis

Sigma-Aldrich

8.20255

Carbazole

Carprofen Related Compound A Pharmaceutical Secondary Standard; Certified Reference Material

Supelco

PHR1564

Carprofen Related Compound A

technique(s)

titration: suitable

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

technique(s)

-

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

color

white to tan

color

-

color

-

color

-

solubility

acetone: 50 mg/mL

solubility

-

solubility

-

solubility

-

form

powder

form

-

form

powder

form

-

application(s)

diagnostic assay manufacturing
hematology
histology

application(s)

clinical
environmental

application(s)

-

application(s)

pharmaceutical (small molecule)

assay

≥95% (GC)

assay

-

assay

≥95.0% (GC)

assay

-

Analysis Note

May contain dark particles.

Application

Carbazole has been used in the uronic acid assay.[1]

Biochem/physiol Actions

Carbazole mainly interacts with DNA and damages it. These events suppress the synthesis of new DNA or RNA. Carbazole derivatives are involved in antimicrobial, antitumor, antiepileptic, antihistaminic, antioxidant, anti-inflammatory, antidiarrhoeal, analgesic, neuroprotective, and pancreatic lipase suppression activities.

General description

Carbazole is an aromatic heterocyclic organic molecule.

pictograms

Health hazard
GHS08

signalword

Warning

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
BCCN1607
BCCM1268
BCCK0009
BCCH0891
BCCD0936

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CARBAZOLE DERIVATIVES IN CANCER TREATMENT-A REVIEW.
Kanneti Naga M, et al.
World Journal of Pharmacy and Pharmaceutical Sciences (2015)
A complete set of hyaluronan fragments obtained from hydrolysis catalyzed by hyaluronidase: Application to studies of hyaluronan mass distribution by simple HPLC devices.
Tranchepain F, et al.
Analytical Biochemistry, 348, 232-242 (2006)
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
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
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
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