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Merck
CN

D139459

4-(Dimethylamino)benzoic acid

98%, for peptide synthesis

Synonym(s):

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

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About This Item

Linear Formula:
(CH3)2NC6H4CO2H
CAS Number:
619-84-1
Molecular Weight:
165.19
NACRES:
NA.22
PubChem Substance ID:
24893426
UNSPSC Code:
12352106
EC Number:
210-615-8
MDL number:
MFCD00002537
Beilstein/REAXYS Number:
386867

Key Documents

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Product Name

4-(Dimethylamino)benzoic acid, 98%

InChI key

YDIYEOMDOWUDTJ-UHFFFAOYSA-N

InChI

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

SMILES string

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

assay

98%

form

powder and chunks

reaction suitability

reaction type: solution phase peptide synthesis

mp

241-243 °C (dec.) (lit.)

application(s)

peptide synthesis

Quality Level

200

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Related Categories

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
STBL3524
STBK6955
STBK9919
STBJ4951
STBJ2144

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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.
Y Hino et al.
Journal of analytical toxicology, 24(3), 165-169 (2000-04-25)
A sensitive and reliable method was developed for the determination of tetracaine and its metabolite, p-butylaminobenzoic acid, in human samples. Tetracaine and the metabolite, effectively extracted using a liquid-liquid extraction procedure from 0.5 g of sample, were analyzed by gas
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
William F Regnault et al.
Journal of materials science. Materials in medicine, 19(2), 507-515 (2007-07-11)
Urethane dimethacrylate (UDMA), an oligomeric poly(ethylene glycol) extended UDMA (PEG-U) and a blend of UDMA/PEG-U were chosen as model systems for introducing both hydrophobic and hydrophilic segments and a range of compliances in their derived polymers. Experimental composites based on
Slow-acting amine polymerization accelerators. Para-dimethylaminobenzoic acid and its ethyl ester.
J M Antonucci et al.
Journal of dental research, 60(7), 1325-1331 (1981-07-01)
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