4-Acetamidobenzoic acid
Suppliers
Names
[ CAS No. ]:
556-08-1
[ Name ]:
4-Acetamidobenzoic acid
[Synonym ]:
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
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
MSDS
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
Precursor & DownStream
Precursor
DownStream
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%
Articles
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...
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 ...
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...