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Merck

D139459

Sigma-Aldrich

4-(Dimethylamino)benzoic acid

98%, for peptide synthesis

Sinónimos:

N,N-Dimethyl-4-aminobenzoic acid, N,N-Dimethyl-p-aminobenzoic acid, p-(Dimethylamino)benzoic acid

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About This Item

Fórmula lineal:
(CH3)2NC6H4CO2H
Número de CAS:
Peso molecular:
165.19
Beilstein/REAXYS Number:
386867
EC Number:
MDL number:
UNSPSC Code:
12352106
PubChem Substance ID:
NACRES:
NA.22

product name

4-(Dimethylamino)benzoic acid, 98%

Quality Level

assay

98%

form

powder and chunks

reaction suitability

reaction type: solution phase peptide synthesis

mp

241-243 °C (dec.) (lit.)

application(s)

peptide synthesis

SMILES string

CN(C)c1ccc(cc1)C(O)=O

InChI

1S/C9H11NO2/c1-10(2)8-5-3-7(4-6-8)9(11)12/h3-6H,1-2H3,(H,11,12)

InChI key

YDIYEOMDOWUDTJ-UHFFFAOYSA-N

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Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves


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Y B Jiang et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 56(4), 623-627 (2000-05-04)
Photoinduced intramolecular charge transfer (ICT) of p-N,N-dimethylaminobenzoic acid (DMABOA) in AOT/cyclohexane/H2O reverse micelle was investigated and compared with that in CTAB/1-heptanol/H2O reverse micelle. It is proposed that the DMABOA molecule exists at the AOT reverse micelle water pool interface with
Xiaoming Xu et al.
Dental materials : official publication of the Academy of Dental Materials, 22(11), 1014-1023 (2005-12-28)
The aims of this study were to formulate a novel fluoride-releasing dental composite and to evaluate its mechanical properties, fluoride release and recharge capabilities, water sorption and solubility. A fluoride-releasing dimethacrylate monomer containing a ternary zirconium fluoride chelate was synthesized.
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The purpose of this study was to evaluate the effects of photoinitiator type and water content on the polymerization rate (Rp) and degree of conversion (DC) of a model BisGMA/HEMA-based resin. The comonomer mixture consisted of BisGMA/HEMA (60/40 by weight).
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Biochemistry, 23(2), 299-304 (1984-01-17)
The imidazole of chromophoric p-(dimethylamino)benzoic acid, DABIm, reacts with the serine protease alpha-chymotrypsin in the pH range of 4-7 to form a stable acyl intermediate that gives very good resonance-enhanced Raman spectra. The resonance Raman and absorption spectra of the

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