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67309

Kovac-Reagenz für Indole

suitable for microbiology

Synonym(e):

4-Dimethylamino-benzaldehyd -Lösung

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100 ML

44,60 €

44,60 €


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Über diesen Artikel

Empirische Formel (Hill-System):
C9H11NO
CAS-Nummer:
Molekulargewicht:
149.19
UNSPSC Code:
41171621
NACRES:
NA.85
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
4132845

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Unterstützung erhalten

Produktname

Kovac-Reagenz für Indole, suitable for microbiology

InChI

1S/C9H11NO/c1-10(2)9-5-3-8(7-11)4-6-9/h3-7H,1-2H3

SMILES string

[H]C(=O)c1ccc(cc1)N(C)C

InChI key

BGNGWHSBYQYVRX-UHFFFAOYSA-N

agency

according to ISO 16654:2001

product line

BioChemika

shelf life

limited shelf life, expiry date on the label

composition

4-(dimethlyamino)benzaldehyde, 50 g/L
hydrochloric acid, 240 g/L
isoamylic alcohol, 710 g/L

technique(s)

microbe id | specific enzyme detection: suitable

application(s)

agriculture
clinical testing
environmental
food and beverages

microbiology

storage temp.

2-8°C

suitability

Escherichia coli
coliforms

Quality Level

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Dieser Artikel
1.09293609831.11350
Quality Level

200

Quality Level

200

Quality Level

100

Quality Level

100

storage temp.

2-8°C

storage temp.

2-8°C

storage temp.

2-8°C

storage temp.

2-8°C

agency

according to ISO 16654:2001

agency

-

agency

-

agency

-

product line

BioChemika

product line

-

product line

-

product line

-

shelf life

limited shelf life, expiry date on the label

shelf life

-

shelf life

limited shelf life, expiry date on the label

shelf life

-

composition

4-(dimethlyamino)benzaldehyde, 50 g/L

composition

-

composition

n-butanol , 4-dimethylaminobenzaldehyde , hydrochloric acid

composition

(n-Butanol; Hydrochloric acid; 4 dimethylaminobenzaldehyde)

Application

In Anwesenheit von Sauerstoff können ein paar Bakterien, z.B. E. coli, Tryptophan in Indol und alpha-Aminopropionsäure aufspalten. Dieses Reagenz dient zur Detektion von Indol und zur Identifizierung von indol-positiven und indol-negativen Mikroorganismen.
Kovac′s reagent may be used for spot test for determination of indole by saturating filter paper with the reagent.[1] It may also be used for initial spot test for determination of indole followed by quantification by spectrophotometric assay and HPLC-UV/Vis-MS/MS methods.[2]

General description

Kovac′s reagent is prepared by mixing p-dimethylaminobenzaldehyde, isoamyl alcohol and concentrated hydrochloric acid.[3] For identification of an organism, the formation of Indole from a tryptophan substrate is a useful diagnostic tool. Indole production is a crucial test in identification of Escherichia coli. After incubation, adding the reagent will help in determination if Indole that has been produced. The reagent turns red when reacts with Indole.[4]

Comparable product

Produkt-Nr.
Beschreibung
Preisangaben

target_organs

Respiratory system

signalword

Danger

Hazard Classifications

Acute Tox. 4 Inhalation - Eye Dam. 1 - Flam. Liq. 3 - Met. Corr. 1 - Skin Corr. 1B - Skin Sens. 1 - STOT SE 3

Lagerklasse

3 - Flammable liquids

wgk

WGK 3

flash_point_f

109.4 °F

flash_point_c

43 °C

ppe

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter


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In der Dokumentenbibliothek finden Sie die Dokumentation zu den Produkten, die Sie kürzlich erworben haben.

Die Dokumentenbibliothek aufrufen

Rita R. Colwell, R. Grigorova
Methods in Microbiology, 19, 27-27 (1987)
S. Harisha
An Introduction to Practical Biotechnology, 193-193 (2005)
Patrick R Porubsky et al.
Archives of biochemistry and biophysics, 475(1), 14-17 (2008-04-22)
Cytochrome P450 2A13 (CYP2A13) is a lung specific enzyme known to activate the potent tobacco procarcinogen 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK) into two carcinogenic metabolites. CYP2A13 has been crystallized and X-ray diffraction experiments illuminated the structure of this enzyme, but with an unknown
Jun-Min Guo et al.
Journal of agricultural and food chemistry, 58(11), 6556-6561 (2010-05-15)
A simple colorimetric method for the differentiation of indoleacetic acid (IAA) and indolebutyric acid (IBA) in plant samples is described. The color change is based upon the reaction between the auxins and p-(dimethylamino)benzaldehyde (PDAB, Ehrlich reagent) following the electrophilic substitution
R W Trepeta et al.
Journal of clinical microbiology, 19(2), 172-174 (1984-02-01)
Escherichia coli is the most common gram-negative microbe isolated and identified in clinical microbiology laboratories. It can be identified within 1 h by oxidase, indole, lactose, and beta-glucuronidase tests. The oxidase and indole tests are performed as spot tests, and

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