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Merck
CN

03005

Sigma-Aldrich

3-Amino-9-ethylcarbazole

20 mg/tablet

Synonym(s):

9-Ethylcarbazol-3-amine, AEC

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About This Item

Empirical Formula (Hill Notation):
C14H14N2
CAS Number:
132-32-1
Molecular Weight:
210.27
Beilstein:
174969
EC Number:
205-057-7
MDL number:
MFCD00004964
UNSPSC Code:
12352204

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concentration

20 mg/tablet

solubility

DMF: 1 tablet/5 mL, clear, dark orange-brown

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

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Biochem/physiol Actions

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.

Other Notes

Peroxidase substrate for immunoblotting and immunohistochemical staining procedures; Hydrosoluble fluorogenic substrate for plasmin

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CYTOCHEMICAL DEMONSTRATION OF PEROXIDASE ACTIVITY WITH 3-AMINO-9-ETHYLCARBAZOLE.
R C GRAHAM et al.
The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society, 13, 150-152 (1965-02-01)
Letter: Substitute for benzidine in myeloperoxidase stains.
I S Kaplow
American journal of clinical pathology, 63(3), 451-451 (1975-03-01)
M Harnois-Pontoni et al.
Analytical biochemistry, 193(2), 248-255 (1991-03-02)
New hydrosoluble fluorogenic substrates for plasmin gluconoylpeptidyl-3-amido-9-ethylcarbazole were synthesized. The substitution of the N-terminal end of the peptides by a gluconoyl group prevents the substrates from aminopeptidase degradation and highly increases their hydrosolubility. The substitution of the peptide C-terminal end

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