3,5-Dimethylbenzoic acid
3,5-Dimethylbenzoic acid structure
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Common Name | 3,5-Dimethylbenzoic acid | ||
|---|---|---|---|---|
| CAS Number | 499-06-9 | Molecular Weight | 150.174 | |
| Density | 1.1±0.1 g/cm3 | Boiling Point | 277.9±9.0 °C at 760 mmHg | |
| Molecular Formula | C9H10O2 | Melting Point | 169-171 °C(lit.) | |
| MSDS | Chinese USA | Flash Point | 128.2±13.4 °C | |
| Symbol |
GHS07 |
Signal Word | Warning | |
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Organotin(IV) based anti-HCV drugs: synthesis, characterization and biochemical activity.
Dalton Trans. 44 , 10467-78, (2015) Three new organotin(iv) carboxylates () of 3,5-dimethylbenzoate, have been synthesized and characterized by elemental analysis, FT-IR, multinuclear NMR ((1)H, (13)C and (119)Sn), mass spectrometry and single crystal X-ray structural analysis. Crystallographic... |
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Urinary excretion of dimethylhippuric acids in humans after exposure to trimethylbenzenes.
Int. Arch. Occup. Environ. Health 69(6) , 491-7, (1997) The aim of this study was to determine the urinary excretion of dimethylhippuric acids (DMHAs) in humans after experimental chamber exposure to trimethylbenzene (TMB) vapor. The DMHAs have been put forward as suitable biomarkers of exposure to products contai... |
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Biological monitoring of experimental human exposure to trimethylbenzene.
Sci. Total Environ. 199(1-2) , 73-81, (1997) Trimethylbenzene (TMB) is a component of numerous commercial preparations of organic solvents (Farbasol, Solvesso, Shellsol) used in the chemical, plastics, printing and other industries. TMB is a mixture of three isomers (pseudocumene-1,2,4-TMB; mesitylene-1... |
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Kinetics of elimination of mesitylene and 3,5-dimethylbenzoic acid after experimental human exposure.
Toxicol. Lett. 77(1-3) , 259-64, (1995) The possibility of evaluating occupational exposure to mesitylene based on the determination of unchanged solvent in capillary blood or 3,5-dimethylbenzoic acid in urine was investigated. The volunteers were exposed to mesitylene in a toxicological chamber (r... |
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Biosynthesis of a Cyclic Tautomer1of (3-Methylmaleyl)acetone from 4-Hydroxy-3,5-dimethylbenzoate byPseudomonassp. HH35 but Not byRhodococcus rhodochrousN75
Biochem. Biophys. Res. Commun. 238(1) , 197-201, (1997) Here we report that the bacterial catabolism of 4-hydroxy-3,5-dimethylbenzoic acid 1 takes a different course inRhodococcus rhodochrousN75 andPseudomonassp. strain HH35. The former organism accumulates a degradation metabolite of the acid which we isolated an... |
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Metabolism of 3-chloro-, 4-chloro-, and 3,5-dichlorobenzoate by a pseudomonad.
Appl. Environ. Microbiol. 37(39) , 421-428., (1979) Pseudomonas sp. WR912 was isolated by continuous enrichment in three steps with 3-chloro-, 4-chloro-, and finally 3,5-dichlorobenzoate as sole source of carbon and energy. The doubling times of the pure culture with these growth substrates were 2.6, 3.3, and ... |
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The crystal structure of the inclusion complex of cyclomaltoheptaose (β-cyclodextrin) with 3, 5-dimethylbenzoic acid. Rontoyianni A and Mavridis IM.
J. Incl. Phenom. Mol. Recog. Chem. 18(3) , 211-27, (1994)
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