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Key Documents

A0879

Sigma-Aldrich

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

≥98% (TLC)

Sinônimo(s):

N-(p-Aminobenzoyl)glutamic acid

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About This Item

Fórmula empírica (Notação de Hill):
C12H14N2O5
Número CAS:
Peso molecular:
266.25
Beilstein:
2816320
Número CE:
Número MDL:
Código UNSPSC:
12352209
ID de substância PubChem:
NACRES:
NA.26

product name

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

Nível de qualidade

Ensaio

≥98% (TLC)

forma

powder

cor

off-white to beige

pf

175 °C (dec.)

aplicação(ões)

detection
peptide synthesis

temperatura de armazenamento

−20°C

cadeia de caracteres SMILES

Nc1ccc(cc1)C(=O)N[C@@H](CCC(O)=O)C(O)=O

InChI

1S/C12H14N2O5/c13-8-3-1-7(2-4-8)11(17)14-9(12(18)19)5-6-10(15)16/h1-4,9H,5-6,13H2,(H,14,17)(H,15,16)(H,18,19)/t9-/m0/s1

chave InChI

GADGMZDHLQLZRI-VIFPVBQESA-N

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Aplicação

N-(4-Aminobenzoyl)-L-glutamic acid (ABG) is used as a strong UV absorbing tag for the derivitization of oligosaccharides to enhance their detection in analytical methods such as capillary zone electrophoresis (CZE).

Ações bioquímicas/fisiológicas

N-p-Aminobenzoyl)-L-glutamic acid is a folate catabolite that can be metabolized by bacterial p-aminobenzoate auxotrophs possessing the enzyme p-aminobenzoyl-glutamate hydrolase.

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Equipamento de proteção individual

Eyeshields, Gloves, type N95 (US)


Certificados de análise (COA)

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J Plocek et al.
Journal of chromatography. A, 757(1-2), 215-223 (1997-01-03)
A charged and strongly UV-absorbing tag, N-(4-aminobenzoyl)-L-glutamic acid) (ABG), was coupled to oligosaccharides by reductive amination under mild conditions. The effectiveness of ABG as a derivatization agent is shown through the separation of isomaltooligosaccharides from a dextran hydrolysate. The minimum
M Laura Dántola et al.
Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology, 9(12), 1604-1612 (2010-10-06)
Folic acid, or pteroyl-l-glutamic acid (PteGlu), is a precursor of coenzymes involved in the metabolism of nucleotides and amino acids. PteGlu is composed of three moieties: a 6-methylpterin (Mep) residue, a p-aminobenzoic acid (PABA) residue, and a glutamic acid (Glu)
Densitometric determination of impurities in drugs: Part IV. Determination of N-(4-aminobenzoyl)-L-glutamic acid in preparations of folic acid.
J Krzek et al.
Journal of pharmaceutical and biomedical analysis, 21(2), 451-457 (2000-03-07)
Yumei Lin et al.
The American journal of clinical nutrition, 80(3), 680-691 (2004-08-24)
A quantitative understanding of human folate metabolism is needed. The objective was to quantify and interpret human folate metabolism as it might occur in vivo. Adults (n = 13) received 0.5 nmol [(14)C]pteroylmonoglutamate (100 nCi radioactivity) plus 79.5 nmol pteroylmonoglutamate
Giuseppe Orsomando et al.
The Plant journal : for cell and molecular biology, 46(3), 426-435 (2006-04-21)
Folates in vivo undergo oxidative cleavage, giving pterin and p-aminobenzoylglutamate (pABAGlu) moieties. These breakdown products are excreted in animals, but their fate is unclear in microorganisms and unknown in plants. As indirect evidence from this and previous studies strongly suggests

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