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133337

Sigma-Aldrich

4-Acetamidobenzoic acid

98%

Synonym(s):

N-Acetyl-PABA

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About This Item

Linear Formula:
CH3CONHC6H4CO2H
CAS Number:
556-08-1
Molecular Weight:
179.17
Beilstein:
390602
EC Number:
209-114-7
MDL number:
MFCD00002534
UNSPSC Code:
12352106
eCl@ss:
32160406
PubChem Substance ID:
24848102
NACRES:
NA.22

Quality Level

200

Assay

98%

form

powder

reaction suitability

reaction type: solution phase peptide synthesis

mp

259-262 °C (dec.) (lit.)

application(s)

peptide synthesis

SMILES string

CC(=O)Nc1ccc(cc1)C(O)=O

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)

InChI key

QCXJEYYXVJIFCE-UHFFFAOYSA-N

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Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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
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
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
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
M Yasuhara et al.
Biochemical pharmacology, 33(20), 3131-3136 (1984-10-15)
The metabolic and excretory function of the small intestine was investigated after oral and intravenous administration of drugs having an aromatic amino group to rats. After administration of drugs into the intestinal loop at the initial concentration of 0.1 mM
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