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D139459

Sigma-Aldrich

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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25 G
CZK 1,200.00
100 G
CZK 1,605.00

CZK 1,200.00

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25 G
CZK 1,200.00
100 G
CZK 1,605.00

About This Item

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

CZK 1,200.00

Please contact Customer Service for Availability
Request a Bulk Order

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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Related Categories

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

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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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
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
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.
Ming Tian et al.
Dental materials : official publication of the Academy of Dental Materials, 24(2), 235-243 (2007-06-19)
To investigate the reinforcement of Bis-GMA/TEGDMA dental resins (without conventional glass filler) and composites (with conventional glass filler) with various mass fractions of nano fibrillar silicate (FS). Three dispersion methods were studied to separate the silanized FS as nano-scaled single
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