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429767

Sigma-Aldrich

4-Aminobenzoic acid

purified by sublimation, ≥99%

Sinónimos:

PABA, Vitamin Bx, Vitamin H1

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About This Item

Fórmula lineal:
H2NC6H4CO2H
Número de CAS:
150-13-0
Peso molecular:
137.14
Beilstein/REAXYS Number:
471605
EC Number:
205-753-0
MDL number:
MFCD00007894
UNSPSC Code:
12352106
eCl@ss:
32160406
PubChem Substance ID:
24866888
NACRES:
NA.22

Quality Level

100

assay

≥99%

form

solid

purified by

sublimation

reaction suitability

reaction type: solution phase peptide synthesis

mp

187-189 °C (lit.)

density

1.374 g/mL at 25 °C (lit.)

application(s)

peptide synthesis

SMILES string

Nc1ccc(cc1)C(O)=O

InChI

1S/C7H7NO2/c8-6-3-1-5(2-4-6)7(9)10/h1-4H,8H2,(H,9,10)

InChI key

ALYNCZNDIQEVRV-UHFFFAOYSA-N

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Categorías relacionadas

hcodes

H412

Hazard Classifications

Aquatic Chronic 3

Storage Class

11 - Combustible Solids

wgk_germany

WGK 2

flash_point_f

339.8 °F - closed cup

flash_point_c

171 °C - closed cup

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves

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Certificados de análisis (COA)

Lot/Batch Number
0000314486
0000319532
MKBP8814V
MKBL7138V
MKBF2263

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Kirk E Hevener et al.
Journal of medicinal chemistry, 53(1), 166-177 (2009-11-11)
Dihydropteroate synthase (DHPS) is a key enzyme in bacterial folate synthesis and the target of the sulfonamide class of antibacterials. Resistance and toxicities associated with sulfonamides have led to a decrease in their clinical use. Compounds that bind to the
Shu-Ting Chen et al.
Journal of the American Society for Mass Spectrometry, 23(8), 1408-1418 (2012-06-08)
A strategy based on negative ion electrospray ionization tandem mass spectrometry and closed-ring labeling with both 8-aminopyrene-1,3,6-trisulfonate (APTS) and p-aminobenzoic acid ethyl ester (ABEE) was developed for linkage and branch determination of high-mannose oligosaccharides. X-type cross-ring fragment ions obtained from
L O Derewlany et al.
The Journal of pharmacology and experimental therapeutics, 269(2), 756-760 (1994-05-01)
The fetus is exposed to almost all of the substances found in the maternal circulation whether nutrients or foreign chemicals ("xenobiotics"). The main route of exposure is the placenta. The placenta is metabolically active toward xenobiotics and the nature of
Steven C Bremmer et al.
Chemical communications (Cambridge, England), 48(44), 5482-5484 (2012-04-28)
A modular system for detecting protease activity via enzyme-triggered gel formation is described. Protease-specific recognition sequences are utilized to achieve enzyme specificity. Artificial blood clotting is demonstrated by activating endogenous thrombin to trigger gelation in fibrinogen-deficient blood plasma.
L O Derewlany et al.
The Journal of pharmacology and experimental therapeutics, 269(2), 761-765 (1994-05-01)
Studies in our laboratory have shown that the N-acetylation activity of the human term placenta is a predominantly attributable to the NAT1 form of arylamine N-acetyltransferase (NAT). To further assess the acetylation capacity of the placenta, the N-acetylation of the
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