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この商品について
化学式:
(CH3)2NC6H4CHO
CAS番号:
分子量:
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
Quality 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-(ジメチルアミノ)ベンズアルデヒド(DMABまたはエールリッヒ試薬)は、ヒドロキシプロリンレベルの定量の呈色試薬として使用されています。ピロールおよび一級アミンと共に発色した凝集物(シッフ塩基)を形成します。’DMABは、紙表面の隠れた指紋を現像して、色付きで蛍光発光の痕跡を得るための試薬としても適しています。
ピロールや第一級アミンと有色の縮合物(シッフ塩基)を形成します。
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signalword
Warning
hcodes
Hazard Classifications
Skin Sens. 1B
保管分類
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)
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
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
