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D139459

Sigma-Aldrich

4-(Dimethylamino)benzoesäure

98%, for peptide synthesis

Synonym(e):

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

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About This Item

Lineare Formel:
(CH3)2NC6H4CO2H
CAS-Nummer:
619-84-1
Molekulargewicht:
165.19
Beilstein:
386867
EG-Nummer:
210-615-8
MDL-Nummer:
MFCD00002537
UNSPSC-Code:
12352106
PubChem Substanz-ID:
24893426
NACRES:
NA.22

product name

4-(Dimethylamino)benzoesäure, 98%

Assay

98%

Form

powder and chunks

Eignung der Reaktion

reaction type: solution phase peptide synthesis

mp (Schmelzpunkt)

241-243 °C (dec.) (lit.)

Anwendung(en)

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)

InChIKey

YDIYEOMDOWUDTJ-UHFFFAOYSA-N

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Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

dust mask type N95 (US), Eyeshields, Gloves

Analysenzertifikate (COA)

Suchen Sie nach Analysenzertifikate (COA), indem Sie die Lot-/Chargennummer des Produkts eingeben. Lot- und Chargennummern sind auf dem Produktetikett hinter den Wörtern ‘Lot’ oder ‘Batch’ (Lot oder Charge) zu finden.

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Sigma-Aldrich

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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.
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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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