4-Acetamidobenzoic acid

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

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]:

Research Areas >> Others

Signaling Pathways >> Others >> Others

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

Click to get detail 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

Click to get detail 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

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...

Related Compounds

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