T36803
p-Toluic acid
98%
Synonym(s):
4-Methylbenzoic acid
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About This Item
Linear Formula:
CH3C6H4CO2H
CAS Number:
Molecular Weight:
136.15
Beilstein:
507600
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Assay
98%
bp
274-275 °C (lit.)
mp
177-180 °C (lit.)
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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Related Categories
Application
- One-Pot Synthesis of 1,3-Cyclohexadienes by Birch Reduction in the Presence of Carbonyl Compounds.: This paper presents a novel synthetic approach involving p-Toluic acid, useful for chemists and researchers in synthetic chemistry aiming to develop more efficient synthesis routes (Linker et al., 2024).
Signal Word
Warning
Hazard Statements
Precautionary Statements
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
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
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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
Qingjiang Wang et al.
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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
Olga Grechishkina
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The retention of aromatic carboxylic acids and their esters in reversed-phase HPLC is proportional to the sum of their partition coefficients in octanol-water system and retention increments. This equation can be used for the identification of various side-products formed in
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