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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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D139459-25G

$43.69

D139459-100G

$112.50

$43.69

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About This Item

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

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Product Name

4-(Dimethylamino)benzoic acid, 98%

Quality Level

200

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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1 of 4

This Item
119695A08798.14621
4-(Dimethylamino)benzoic acid 98%

Sigma-Aldrich

D139459

4-(Dimethylamino)benzoic acid

4-(Methylamino)benzoic acid 97%

Sigma-Aldrich

119695

4-(Methylamino)benzoic acid

N-(4-Aminobenzoyl)-L-glutamic acid ≥98% (TLC)

Sigma-Aldrich

A0879

N-(4-Aminobenzoyl)-L-glutamic acid

4-Aminohippuric acid for synthesis

Sigma-Aldrich

8.14621

4-Aminohippuric acid

form

powder and chunks

form

-

form

powder

form

solid

assay

98%

assay

97%

assay

≥98% (TLC)

assay

≥98.0% (HPLC)

Quality Level

200

Quality Level

100

Quality Level

200

Quality Level

200

mp

241-243 °C (dec.) (lit.)

mp

160-162 °C (lit.)

mp

175 °C (dec.)

mp

199-202 °C (decomposition)

reaction suitability

reaction type: solution phase peptide synthesis

reaction suitability

reaction type: solution phase peptide synthesis

reaction suitability

-

reaction suitability

-

application(s)

peptide synthesis

application(s)

peptide synthesis

application(s)

detection
peptide synthesis

application(s)

-

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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Certificates of Analysis (COA)

Lot/Batch Number
STBL3524
STBK6955
STBK9919
STBJ4951
STBJ2144

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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
P V Argade et al.
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
Xinglin Guo et al.
Dental materials : official publication of the Academy of Dental Materials, 24(6), 824-831 (2007-11-30)
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).
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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