grade
purum
분석
≥98.0% (GC)
bp
274-275 °C (lit.)
mp
177-180 °C (lit.)
177-182 °C
SMILES string
Cc1ccc(cc1)C(O)=O
InChI
1S/C8H8O2/c1-6-2-4-7(5-3-6)8(9)10/h2-5H,1H3,(H,9,10)
InChI key
LPNBBFKOUUSUDB-UHFFFAOYSA-N
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신호어
Warning
유해 및 위험 성명서
Hazard Classifications
Skin Sens. 1
Storage Class Code
11 - Combustible Solids
WGK
WGK 1
Flash Point (°F)
357.8 °F
Flash Point (°C)
181 °C
개인 보호 장비
Eyeshields, Gloves, type N95 (US)
Qingjiang Wang et al.
Electrophoresis, 26(17), 3273-3278 (2005-09-07)
For its high reactivity and very short half-life, the hydroxyl radical (OH.) in vivo is very difficult to be detected. Usually, it is indirectly quantified by determining 2,3-dihydroxybenzoic acid (2,3-DHBA) and 2,5-dihydroxybenzoic acid (2,5-DHBA), which are the reaction products of
Robert McGraw et al.
The Journal of chemical physics, 128(6), 064508-064508 (2008-02-20)
Recent kinetic extensions of the nucleation theorem suggest that the logarithm of the steady-state nucleation rate has strong multilinear dependence on the log concentrations of condensable species present in the vapor phase. A further remarkable result is that the coefficients
V Balachandran et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 104, 114-129 (2012-12-26)
FT-Raman and FT-IR spectra for 2-hydroxy-p-toluic acid molecule had been recorded in the regions 3500-100 cm(-1) and 4000-400 cm(-1), respectively. Vibrational frequencies have been calculated in optimum state by employing density functional theory (DFT) and Hartree Fock (HF) methods with
T Arras et al.
Journal of bacteriology, 180(8), 2133-2136 (1998-04-29)
The growth rates of Pseudomonas putida KT2442 and mt-2 on benzoate, 4-hydroxybenzoate, or 4-methylbenzoate showed an exponential decrease with decreasing oxygen tensions (partial O2 tension [pO2] values). The oxygen tensions resulting in half-maximal growth rates were in the range of
Sven Lahme et al.
Applied and environmental microbiology, 78(5), 1606-1610 (2011-12-20)
A novel alphaproteobacterium isolated from freshwater sediments, strain pMbN1, degrades 4-methylbenzoate to CO(2) under nitrate-reducing conditions. While strain pMbN1 utilizes several benzoate derivatives and other polar aromatic compounds, it cannot degrade p-xylene or other hydrocarbons. Based on 16S rRNA gene
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