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Merck

D2004

Sigma-Aldrich

4-(Dimethylamino)benzaldehyd

suitable for histochemical demonstration of nitro blue tetrazolium reduction in neutrophils

Synonym(e):

Ehrlich-Reagens

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About This Item

Lineare Formel:
(CH3)2NC6H4CHO
CAS-Nummer:
Molekulargewicht:
149.19
Beilstein:
606802
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
12171500
PubChem Substanz-ID:
NACRES:
NA.47

Assay

≥99% (TLC)

Form

powder

mp (Schmelzpunkt)

72-75 °C (lit.)

Löslichkeit

ethanol: 50 mg/mL

Eignung

suitable for histochemical demonstration of nitro blue tetrazolium reduction in neutrophils

Anwendung(en)

diagnostic assay manufacturing
hematology
histology

Lagertemp.

room temp

SMILES String

CN(C)c1ccc(C=O)cc1

InChI

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

InChIKey

BGNGWHSBYQYVRX-UHFFFAOYSA-N

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Anwendung

4-(Dimethylamino)benzaldehyde (DMAB or Ehrlich’s reagent) has been used as a color reagent for the determination of hydroxyproline level.It forms colored condensation products (Schiff bases) with pyrroles and primary amines. DMAB is also suitable as a reagent to develop latent fingermarks on paper surfaces yielding impressions that are both colored and photoluminescent.
Bildet farbige Kondensationsprodukte (Schiff sche Basen) mit Pyrrolen und primären Aminen.

Piktogramme

Exclamation mark

Signalwort

Warning

H-Sätze

Gefahreneinstufungen

Skin Sens. 1B

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 1

Flammpunkt (°F)

327.2 °F - closed cup

Flammpunkt (°C)

164 °C - closed cup

Persönliche Schutzausrüstung

Eyeshields, Gloves, type N95 (US)


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Jamie Morrison et al.
The American journal of pathology, 166(6), 1701-1710 (2005-05-28)
Duchenne muscular dystrophy was initially described as a myosclerosis because of the conspicuous progression of interstitial fibrosis. Using the mdx mouse homologue, we have shown previously that the accumulation of intramuscular collagen is profoundly influenced by the presence or absence
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
Spectrophotometric determination of certain cephalosporins through oxidation with cerium(IV) and 1-chlorobenzotriazole.
M M Ayad et al.
Journal of pharmaceutical and biomedical analysis, 20(3), 557-564 (2000-03-04)
M Stefek et al.
Biochimica et biophysica acta, 1502(3), 398-404 (2000-11-09)
In the present work, pepsin digests of tail tendons from streptozotocin-diabetic rats were found to contain material that reacted rapidly at room temperature with p-dimethylaminobenzaldehyde (Ehrlich's reagent) to give an adduct with an absorbance spectrum characteristic of the Ehrlich chromogen
Rosario Zamora et al.
Journal of agricultural and food chemistry, 52(13), 4166-4171 (2004-06-24)
The Ehrlich reaction was optimized to determine the formation of pyrrolized phospholipids in edible oils in an attempt to understand the color reversion produced during the deodorization of poorly degummed edible oils. The procedure consisted of the treatment of the

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