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D139459

Sigma-Aldrich

4-(Dimethylamino)benzoic acid

98%, for peptide synthesis

Sinonimo/i:

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

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About This Item

Formula condensata:
(CH3)2NC6H4CO2H
Numero CAS:
619-84-1
Peso molecolare:
165.19
Beilstein:
386867
Numero CE:
210-615-8
Numero MDL:
MFCD00002537
Codice UNSPSC:
12352106
ID PubChem:
24893426
NACRES:
NA.22

product name

4-(Dimethylamino)benzoic acid, 98%

Livello qualitativo

200

Saggio

98%

Forma fisica

powder and chunks

Impiego in reazioni chimiche

reaction type: solution phase peptide synthesis

Punto di fusione

241-243 °C (dec.) (lit.)

applicazioni

peptide synthesis

Stringa SMILE

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)
YDIYEOMDOWUDTJ-UHFFFAOYSA-N

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Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

dust mask type N95 (US), Eyeshields, Gloves

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Certificati d'analisi (COA)

Lot/Batch Number
STBJ4951
STBJ2144
STBH9668
STBD9675V
STBC9771V

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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
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
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.
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).
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