4-Acetamidobenzoic acid structure
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Common Name | 4-Acetamidobenzoic acid | ||
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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 acidAcedoben is a biochemical reagent that can be used as a biological material or organic compound for life science related research. |
Name | 4-acetamidobenzoic acid |
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Synonym | More Synonyms |
Description | Acedoben is a biochemical reagent that can be used as a biological material or organic compound for life science related research. |
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Related Catalog |
Density | 1.3±0.1 g/cm3 |
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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 |
Precursor 10 | |
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DownStream 10 | |
HS Code | 2924299090 |
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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% |
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... |
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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 ... |
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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... |
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 |