4-Acetamidobenzoic acid

Modify Date: 2025-08-20 18:27:07

4-Acetamidobenzoic acid Structure
4-Acetamidobenzoic acid structure
 Common Name 4-Acetamidobenzoic acid
CAS Number 556-08-1 Molecular Weight 179.17
Density 1.3±0.1 g/cm3 Boiling Point 439.6±28.0 °C at 760 mmHg
Molecular Formula C9H9NO3 Melting Point 259-262 °C (dec.)(lit.)
MSDS Chinese USA Flash Point 219.7±24.0 °C

 Use of 4-Acetamidobenzoic acid


Acedoben is a biochemical reagent that can be used as a biological material or organic compound for life science related research.

 Names

Name 4-acetamidobenzoic acid
Synonym More Synonyms

 4-Acetamidobenzoic acid Biological Activity

Description Acedoben is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
Related Catalog

 Chemical & Physical Properties

Density 1.3±0.1 g/cm3
Boiling Point 439.6±28.0 °C at 760 mmHg
Melting Point 259-262 °C (dec.)(lit.)
Molecular Formula C9H9NO3
Molecular Weight 179.17
Flash Point 219.7±24.0 °C
Exact Mass 179.058243
PSA 66.40000
LogP 1.31
Vapour Pressure 0.0±1.1 mmHg at 25°C
Index of Refraction 1.620
Stability Stable. Combustible. Incompatible with strong oxidizing agents.
Water Solubility <0.1 g/100 mL at 21 ºC

 Safety Information

Personal Protective Equipment Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
Hazard Codes Xi
Risk Phrases R36/37/38
Safety Phrases S24/25
RIDADR NONH for all modes of transport
WGK Germany 3
HS Code 2924299090

 Synthetic Route

 Customs

HS Code 2924299090
Summary 2924299090. other cyclic amides (including cyclic carbamates) and their derivatives; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

 Articles28

More Articles
Comparison of xenobiotic metabolizing enzyme activities in ex vivo human skin and reconstructed human skin models from SkinEthic.

Arch. Toxicol. 88(9) , 1681-1694, (2014)

Skin function is not limited to a physical barrier. According to its total surface area, it is also considered as an extra-hepatic metabolizing organ. In vitro engineered human skins have been develop...

Regioselective carboxylation of catechol by 3,4-dihydroxybenzoate decarboxylase of Enterobacter cloacae P.

Biotechnol. Lett. 32(5) , 701-5, (2010)

3,4-Dihydroxybenzoate decarboxylase in Enterobacter cloacae P241 was induced by adding 3,4-dihydroxybenzoic acid, 3-hydroxybenzoic acid, 3,4,5-trihydroxybenzoic acid or 4-acetamidobenzoic acid to the ...

Effects of butylated hydroxyanisole and butylated hydroxytoluene on DNA adduct formation and arylamine N-acetyltransferase activity in human bladder tumour cells.

J. Appl. Toxicol. 22(1) , 37-44, (2002)

In this study, butylated hydroxyanisole (BHA) and butylated hydroxytoluene (BHT) were used to determine the inhibition of arylamine N-acetyltransferase (NAT) activity and DNA adduct formation in human...

 Synonyms

4-(acetylamino)benzoic acid
acedobene
Benzoic acid, 4-(acetylamino)-
EINECS 209-114-7
p-Acetylamino benzoic acid
p-acetylaminobenzoic acid
acedobenum
Acedoben
p-Acetylamino-benzoic acid
N-ACETYL-PABA
4-acetaminobenzoic acid
PAABA
p-Carboxyacetanilide
4-acetamidobenzoic_acid
para-acetamidobenzoic acid
LR-64
p-Acetaminobenzoic acid
ACETYLATED PABA
RARECHEM AL BO 0055
4-Acetylaminobenzoic acid
4-Acetamidobenzoic acid
PAAB
N-acetyl-4-aminobenzoic acid
4-(acetylamino)benzenecarboxylic acid
Acedoben [INN]
MFCD00002534
p-acetamidobenzoic
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