D149608
3,5-Dimethylbenzoic acid
99%
Sinónimos:
Mesitylenic acid, sym.-m-Xylylic acid
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About This Item
Fórmula lineal:
(CH3)2C6H3CO2H
Número de CAS:
Peso molecular:
150.17
Beilstein/REAXYS Number:
1072182
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
assay
99%
form
crystals
mp
169-171 °C (lit.)
SMILES string
Cc1cc(C)cc(c1)C(O)=O
InChI
1S/C9H10O2/c1-6-3-7(2)5-8(4-6)9(10)11/h3-5H,1-2H3,(H,10,11)
InChI key
UMVOQQDNEYOJOK-UHFFFAOYSA-N
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Storage Class
11 - Combustible Solids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Los clientes también vieron
P Kostrewski et al.
Toxicology letters, 77(1-3), 259-264 (1995-05-01)
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 (range 10-150 mg/m3). Concentrations of
J Järnberg et al.
International archives of occupational and environmental health, 69(6), 491-497 (1997-01-01)
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 containing TMBs
R B Cain et al.
Biochemical and biophysical research communications, 238(1), 197-201 (1997-09-23)
Here we report that the bacterial catabolism of 4-hydroxy-3,5-dimethylbenzoic acid 1 takes a different course in Rhodococcus rhodochrous N75 and Pseudomonas sp. strain HH35. The former organism accumulates a degradation metabolite of the acid which we isolated and identified as
P Kostrzewski et al.
The Science of the total environment, 199(1-2), 73-81 (1997-06-20)
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-1,3,5-TMB; hemimellitene-1,2,3-TMB). The proportion of individual isomers in
Farooq Ali Shah et al.
Dalton transactions (Cambridge, England : 2003), 44(22), 10467-10478 (2015-05-16)
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 data show that in compounds and , the geometry
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