D2004
4-(Dimethylamino)benzaldehyde
suitable for histochemical demonstration of nitro blue tetrazolium reduction in neutrophils
Sinónimos:
p-Dimethylaminobenzaldehyde, DMAB, Ehrlich’s reagent
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Fórmula lineal:
(CH3)2NC6H4CHO
Número CAS:
Peso molecular:
149.19
UNSPSC Code:
12171500
NACRES:
NA.47
PubChem Substance ID:
EC Number:
202-819-0
Beilstein/REAXYS Number:
606802
MDL number:
Assay:
≥99% (TLC)
Form:
powder
Servicio técnico
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Permítanos ayudarleQuality Level
assay
≥99% (TLC)
form
powder
mp
72-75 °C (lit.)
solubility
ethanol: 50 mg/mL
suitability
suitable for histochemical demonstration of nitro blue tetrazolium reduction in neutrophils
application(s)
diagnostic assay manufacturing
hematology
histology
storage temp.
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
InChI key
BGNGWHSBYQYVRX-UHFFFAOYSA-N
Application
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.
Forms colored condensation products (Schiff bases) with pyrroles and primary amines.
signalword
Warning
hcodes
Hazard Classifications
Skin Sens. 1B
Clase de almacenamiento
11 - Combustible Solids
wgk
WGK 1
flash_point_f
327.2 °F - closed cup
flash_point_c
164 °C - closed cup
ppe
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
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
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