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Phenol is an organic compound appreciably soluble in water, with about 84.2 g dissolving in 1000 ml (0.895 M). Homogeneous mixtures of phenol and water at phenol to water mass ratios of ~2.6 and higher are possible. The sodium salt of phenol, sodium phenoxide, is far more water-soluble. It is a combustible solid (NFPA rating = 2).
108-95-2: 0070: Phenol: 962 mg/m 3: 250 ppm: 108952: 106-50-3: 0805: p-Phenylene diamine: 25 mg/m 3-106503: 101-84-8: 0791: Phenyl ether: 100 mg/m 3: 696 ppm: 101848: 122-60-1: 0188: Phenyl glycidyl ether: 614 mg/m 3: 100 ppm: 122601, carcinogenic substance 100-63-0: 0938: Phenylhydrazine: 66.3 mg/m 3: 15 ppm: 100630, carcinogenic substance ...
phenol: 108-95-2 C 6 H 6 O 2: catechol: 120-80-9 hydroquinone: 123-31-9 resorcinol: 108-46-3 C 6 H 6 O 3: hydroxymethylfurfural: 67-47-0 C 6 H 7 BO 2: phenylboronic acid: 98-80-6 C 6 H 7 CsO 6: caesium ascorbate: C 6 H 7 KO 6: potassium ascorbate: Potassium erythorbate: 17175-66-5 C 6 H 7 LiO 6: lithium ascorbate: C 6 H 7 N 3 O: isoniazid: 54 ...
108.057515 C7H6O2: 4-Hydroxybenzaldehyde, others 122.036779 ... 2,4-Bis(4-hydroxybenzyl) phenol 306.125594 C16H20O6: Monocerin 308.1259876 C13H12O9: Caftaric acid
2,4,6-Tris(dimethylaminomethyl)phenol is an aromatic organic chemical that has tertiary amine and phenolic hydroxyl functionality in the same molecule. [1] The formula is C 15 H 27 N 3 O and the CAS Registry Number is 90-72-2. It is REACH registered and the European Community Number is 202-013-9. [2] [3] [4]
Phenol is readily alkylated at the ortho positions using alkenes in the presence of a Lewis acid such as aluminium phenoxide: [citation needed] CH 2 =CR 2 + C 6 H 5 OH → R 2 CHCH 2-2-C 6 H 4 OH. More than 100,000 tons of tert-butyl phenols are produced annually (year: 2000) in this way, using isobutylene (CH 2 =CMe 2) as the alkylating agent
Substance Formula 0 °C 10 °C 20 °C 30 °C 40 °C 50 °C 60 °C 70 °C 80 °C 90 °C 100 °C Barium acetate: Ba(C 2 H 3 O 2) 2: 58.8: 62: 72: 75: 78.5: 77: 75
In female elephants, the two compounds 3-ethyl phenol and 2-ethyl 4,5 dimethylphenol have been detected in urine samples. [70] Temporal glands secretion examination showed the presence of phenol, m-cresol and p-cresol (4-methyl phenol) during musth in male elephants. [71] [72] [73] p-Cresol and o-cresol are also components of the human sweat.