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6- -2,4-dimethylphenol

DMMP was not mutagenic in Salmonella assays. An ACGIH threshold limit value (TLV) has not been established for dimethyl methylphosphonate. [Pg.271]

National Toxicology Program Toxicology and Carcinogenesis Studies of Dimethyl Methylphosphonate in F344/N Rats and B6C3F1 Mice, pp 1-64. NTP TR 323, NIH Pub 87-2579, [Pg.271]

Dunnick JK, Gupta BN, Harris MW, et al Reproductive toxicity of dimethyl methylphosphonate (DMMP) in the male Fischer 344 rat. Toxicol Appl Pharmacol 72 379-387, 1984 [Pg.271]

Chapin RE, Dutton SL, Ross MD, et al Development of reproductive tract lesions in male F344 rats after treatment with dimethyl methylphosphonate. Exp Mol Pathol 41 126-140, 1984 [Pg.271]

Dunnick JK, Eustis SL, Haseman JK Development of kidney tumors in the male F344/N rat after treatment with dimethyl methylphosphonate. Fundam Appl Toxicol 11 91-99, [Pg.271]

5 in H2O very soluble in alcohols, acetone, ether and other organic solvents [Pg.539]

More toxic and corrosive to skin and mucous membranes than cresols (monomethylphenols). Exposure limits (occupational) Germany 19(5) mg/m (ppm) [Pg.539]

Xylenol may be used as an active ingredient in preservatives and disinfectants, but is, however, no longer of practical importance in these applications. [Pg.539]

Microbicide group (substance class) Chemical name Chemical formula Structural formula [Pg.539]

Content i Boiling point/range °C (101 kPa) Melting point °C Density g/ml [Pg.539]


Treatment of 3 5 dimethylphenol with dilute nitnc acid followed by steam distillation of the reaction mixture gave a compound A (CgH9N03 mp 66°C) in 36% yield The nonvolatile residue from the steam distillation gave a compound B (CsHpNOs mp 108°C) in 25% yield on extraction with chloroform Identify compounds A and B... [Pg.1022]


See other pages where 6- -2,4-dimethylphenol is mentioned: [Pg.685]    [Pg.685]    [Pg.685]    [Pg.686]    [Pg.464]    [Pg.1002]    [Pg.1003]    [Pg.1004]    [Pg.1004]    [Pg.432]    [Pg.434]    [Pg.454]    [Pg.454]    [Pg.454]    [Pg.454]    [Pg.473]    [Pg.473]    [Pg.473]    [Pg.473]    [Pg.473]    [Pg.473]    [Pg.519]    [Pg.519]    [Pg.519]    [Pg.519]    [Pg.520]    [Pg.552]    [Pg.552]    [Pg.552]    [Pg.552]    [Pg.552]    [Pg.552]    [Pg.593]    [Pg.593]    [Pg.593]    [Pg.593]    [Pg.593]    [Pg.593]    [Pg.679]    [Pg.679]    [Pg.679]    [Pg.679]    [Pg.679]    [Pg.679]    [Pg.853]    [Pg.863]    [Pg.863]    [Pg.871]   
See also in sourсe #XX -- [ Pg.340 ]

See also in sourсe #XX -- [ Pg.287 ]

See also in sourсe #XX -- [ Pg.18 ]

See also in sourсe #XX -- [ Pg.55 ]




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2, 6-Dimethylphenol, polymerization

2,6-Dimethylphenol oxidative polymerization

2,6-Dimethylphenol polymer

2,6-Dimethylphenol, temperature

2-Amino-3,6-dimethylphenol

2.4- Dibromo-3,6-dimethylphenol

2.4- Dimethylphenol, Mannich reaction

2.4- dichloro-3,5-dimethylphenol

2.6- Dimethylphenol, oxidation

2.6- Dimethylphenol, reaction with

2.6- Xylenol, 2,6-Dimethylphenol

3.4- Methylene-2,5-dimethylphenol

3.5- Dimethylphenol, methylation with

3.5- dimethylphenol production

4- /«7-Butyl-2,5-dimethylphenol

4-Benzyl-2,6-dimethylphenol

4-Bromo-2,6-dimethylphenol

4-Chloro-2,6-dimethylphenol

4-tert-Butyl-2,6-dimethylphenol

Atmospheres dimethylphenol

Coating 2,6-dimethylphenol

Combustion dimethylphenol

Copolymer of 2,6-dimethylphenol

Copolymerization 2,6-dimethylphenol

Coupling polymerization 2,6-dimethylphenol

Cyclohexadienones from 2.6- dimethylphenol

Detection limit dimethylphenol

Dimethylphenol complexes

Dimethylphenol content

Dimethylphenol oxidative coupling

Dimethylphenol reaction pathways

Dimethylphenol reactions

Dimethylphenols

Dimethylphenols

Dimethylphenols, atmosphere

Imidazole Complexes Catalyze the Oxidative Polymerization of 2,6-Dimethylphenol with Dioxygen

Lithium 2,6-dimethylphenoxide, from 2,6-dimethylphenol

Lithium, reaction with 2,6-dimethylphenol

Nitrate with 2,6-dimethylphenol

Polymerization mechanism, 2,6-dimethylphenol

Ricinoleic acid reaction with 2,4-dimethylphenol

Sulfonation 2,6-dimethylphenol

Tribromo-2,6-dimethylphenol

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