133337
4-Acetamidobenzoic acid
98%
Synonym(s):
N-Acetyl-PABA
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About This Item
Linear Formula:
CH3CONHC6H4CO2H
CAS Number:
Molecular Weight:
179.17
NACRES:
NA.22
PubChem Substance ID:
eCl@ss:
32160406
UNSPSC Code:
12352106
EC Number:
209-114-7
MDL number:
Beilstein/REAXYS Number:
390602
Product Name
4-Acetamidobenzoic acid, 98%
InChI key
QCXJEYYXVJIFCE-UHFFFAOYSA-N
InChI
1S/C9H9NO3/c1-6(11)10-8-4-2-7(3-5-8)9(12)13/h2-5H,1H3,(H,10,11)(H,12,13)
SMILES string
CC(=O)Nc1ccc(cc1)C(O)=O
assay
98%
form
powder
reaction suitability
reaction type: solution phase peptide synthesis
mp
259-262 °C (dec.) (lit.)
application(s)
peptide synthesis
Quality Level
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Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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João Neres et al.
Bioorganic & medicinal chemistry, 15(5), 2106-2119 (2007-01-16)
Benzoic acid and pyridine derivatives inhibit recombinant trans-sialidase from Trypanosoma cruzi with I50 values between 0.4 and 1mM. The best compounds, 4-acetylamino-3-hydroxymethylbenzoic acid and 5-acetylamino-6-aminopyridine-2-carboxylic acid, provide new leads to inhibitors not containing the synthetically complex sialic acid structure. The
Yasuhiro Uno et al.
Biochemical pharmacology, 177, 113996-113996 (2020-04-28)
In humans, polymorphic N-acetyltransferases NAT1 and NAT2 are important enzymes that metabolize endogenous and exogenous compounds, including drugs. These enzymes exhibit considerable inter-individual variability in humans. The cynomolgus macaque is a nonhuman primate species that is widely used in drug
J A Kovacs et al.
Antimicrobial agents and chemotherapy, 37(6), 1227-1231 (1993-06-01)
Isoprinosine has been reported to decrease progression to AIDS, primarily by preventing Pneumocystis carinii pneumonia (PCP), in human immunodeficiency virus-infected patients, but the mechanism of action is unknown. para-Acetamidobenzoic acid (PAcBA), one component of isoprinosine, is structurally related to para-aminobenzoic
Lai-Hao Wang et al.
Journal of pharmaceutical and biomedical analysis, 43(4), 1430-1436 (2006-11-23)
p-Aminobenzoic acid (PABA) and its metabolites (p-aminohippuric acid, p-acetamidobenzoic acid, and p-acetamidohippuric acid) were detected using high-performance liquid chromatography with an electrochemical (carbon paste) detector (HPLC-ECD). For direct current (dc) mode, with the current at a constant potential, and measurements
K N Furuya et al.
Clinical biochemistry, 28(5), 531-540 (1995-10-01)
To evaluate glycine conjugation of para-aminobenzoic acid (PABA) to the hippurated metabolites, para-aminohippuric acid (PAHA), and para-acetamidohippuric acid (PAAHA) as a quantitative liver function test in patients with liver disease. Serum concentrations of PABA and metabolites were measured by high
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