Skip to Content
Merck
All Photos(3)

Key Documents

View All Documentation

A5754

Sigma-Aldrich

3-Amino-9-ethylcarbazole

≥95% (HPLC), powder

Synonym(s):

9-Ethylcarbazol-3-amine, AEC

Sign Into View Organizational & Contract Pricing
All Photos(3)

About This Item

Empirical Formula (Hill Notation):
C14H14N2
CAS Number:
132-32-1
Molecular Weight:
210.27
Beilstein:
174969
MDL number:
MFCD00004964
UNSPSC Code:
12352204
PubChem Substance ID:
24891017
NACRES:
NA.83

product name

3-Amino-9-ethylcarbazole, ≥95% (HPLC), powder

Assay

≥95% (HPLC)

form

powder

impurities

≤3% solvent

solubility

ethanol: acetic acid (2:1): 50 mg/mL, clear to hazy

storage temp.

2-8°C

SMILES string

CCn1c2ccccc2c3cc(N)ccc13

InChI

1S/C14H14N2/c1-2-16-13-6-4-3-5-11(13)12-9-10(15)7-8-14(12)16/h3-9H,2,15H2,1H3

InChI key

OXEUETBFKVCRNP-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

General description

3-Amino-9-ethylcarbazole serves as chromogen in immunocytochemistry and produces a red color.

Specificity

3-Amino-9-ethylcarbazole is a peroxidase substrate suitable for use in immunoblotting and immunohistochemical staining procedures. This substrate produces an insoluble end product that is red in color and can be observed visually.

Application

3-Amino-9-ethylcarbazole has been used to visualize the bound primary antibody by using a streptavidin method. It has also been used in visualizing tissue sections from tumour samples.

Substrates

Substrate for peroxidase.

Analysis Note

Actual content given on label

related product

Product No.
Description
Pricing

Pictograms

Skull and crossbonesHealth hazard
GHS06,GHS08

Signal Word

Danger

Hazard Statements

H301,H350

Hazard Classifications

Acute Tox. 3 Oral - Carc. 1B

Storage Class Code

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Patterns of angiogenesis in nonsmall-cell lung carcinoma
Offersen BV, et al.
Cancer, 91(8), 1500-1509 (2001)
VEGF-C and COX-2 expression in papillary thyroid cancer
Siironen P, et al.
Endocrine-Related Cancer, 13(2), 465-473 (2006)
Katharina Dötzer et al.
Cancers, 11(9) (2019-08-29)
CD3+ and CD8+ lymphocytes are well known prognostic markers in primary ovarian cancer. In contrast, the predictive value of the immune infiltrate concerning treatment response and the involvement of immune heterogeneity between primary and metastatic lesions are poorly understood. In
Veronika Mlitz et al.
The Journal of investigative dermatology, 134(11), 2685-2692 (2014-05-02)
S100 fused-type proteins (SFTPs) such as filaggrin, trichohyalin, and cornulin are differentially expressed in cornifying keratinocytes of the epidermis and various skin appendages. To determine evolutionarily conserved, and thus presumably important, features of SFTPs, we characterized nonmammalian SFTPs and compared
Rihab Bouchareb et al.
Circulation, 132(8), 677-690 (2015-08-01)
Mendelian randomization studies have highlighted that lipoprotein(a) [Lp(a)] was associated with calcific aortic valve disease (CAVD). Lp(a) transports oxidized phospholipids with a high content in lysophosphatidylcholine. Autotaxin (ATX) transforms lysophosphatidylcholine into lysophosphatidic acid. We hypothesized that ATX-lysophosphatidic acid could promote
View All Related Papers

Articles

Colorimetric Alkaline Phosphatase and Peroxidase Substrate Detection Systems

Nitroblue Tetrazolium (NBT) is used with the alkaline phosphatase substrate 5-Bromo- 4-Chloro-3-Indolyl Phosphate (BCIP) in western blotting and immunohistological staining procedures. These substrate systems produce an insoluble NBT diformazan end product that is blue to purple in color and can be observed visually.

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service