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4-Hexyl-resorcinol

Hexyl-resorcinol More potent. Used as mouth wash, lozenges as antifungal. [Pg.408]

Burrows D, Irvine J. 1982. Contact dermatitis to hexyl resorcinol. Contact Dermatitis 8 71. [Pg.113]

Spectrophotometric determination with 4-hexyl-resorcinol and a fluorometric method with m-aminophenol are the most commonly... [Pg.4]

Phenol (carbolic acid) is not a sensitizer but a deep skin penetrant producing local gangrene if not diluted. Resorcinol is used for its alleged intipruritic and anti-acne keratolytic properties. It irritates in a dose-related manner but allergic reactions occur (Caron and Calnan 1962 Keil 1962). Group hypersensitivity was demonstrated for some resorcinol derivatives such as resorcinol-mono-acetate and hexyl-resorcinol, which are metadihydroxybenzenes. The ortho and para compounds do not cross-react. [Pg.322]

Hexyl alcohol, acetate. See Hexyl acetate n-Hexyl aldehyde. See Hexanal 4-Hexyl-1,3-benzenediol. See 4-Hexyl resorcinol Hexyl benzoate... [Pg.2032]

Hexyl resorcine Hexyl resorcinol. See4-Hexyl resorcinol 4-Hexyl resorcinol... [Pg.2041]

Basic violet 3 Calcium cyanamide Dichlorophene 4-Hexyl resorcinol Nicotine Wormwood (Artemisia absinthium) oil anthelmintic agent, medicine Sodium arsanilate... [Pg.4814]

The above explanations show two potential reasons for the use of plasticizers the decrease of processing temperature for either the matrix polymer or for PANI or for its derivative. Simple substances such as hydroquinone, resorcinol, tert-butyl hydroquinone, 4-hexyl resorcinol, and bisphenol-A have been used as plasticizers in conjunction with polymethylmethacrylate as the matrix polymer. In addition to improved processability, plasticizers have been helpful in organization of polymer chains (lydrogen bonding and phenyl stacking), which results in better charge transfer between the PANI chains. ... [Pg.300]

Additives used in final products Fillers carbon black, montmorillonite, multiwalled carbon nanotubes, silica Plasticizers hydroquinone, resorcinol, tert-butyl hydroquinone, 4-hexyl resorcinol, bisphenol-A, sulfonic acids, phosphonic acids (phenyl phosphonic acid), and aliphatic dIesters of phosphoric acid (diphenyl, dioctyl and dibutyl) UV absorber Tinuvin 213 ... [Pg.278]

Preparation by reaction of benzotrichloride with 4-hexyl-resorcinol in hydroflnoric acid in the presence of water at -10° for 4 h, then at r.t. overnight (80%) [213]. [Pg.388]

Preparation by reaction of benzoic acid with 4-hexyl-resorcinol in the presence of boron trifluoride in tetrachloroethane on a steam bath for 4 h [113]. [Pg.388]

Preparation by reaction of acetonitrile on 4-n-hexyl-resorcinol (Hoesch reaction) (84%) [2676]. [Pg.992]

Preparation by reaction of trifluoroacetamide on 4-hexyl-resorcinol at reflux, with boron trifluoride etherate (55%) or with p-toluenesulfonic acid (20%) [4689],... [Pg.1282]

Preparation by acylation of 4-(3,5-dime-thylcyclo-hexyl)-resorcinol (1 mol) with trifluoroacetic anhydride (1.2 mol) in the presence of aluminium chloride (2 mol) in ethylene dichloride at r.t. (79%) [4689]. [Pg.1285]

Preparation by reaction of phenylacetonitrile with 4-hexyl-resorcinol,... [Pg.1439]

Obtained by reaction of phenylacetonitrile with 2-hexyl-resorcinol in the presence of zinc chloride (31%) (Hoesch reaction) [6225]. [Pg.1698]

See other pages where 4-Hexyl-resorcinol is mentioned: [Pg.687]    [Pg.687]    [Pg.687]    [Pg.85]    [Pg.17]    [Pg.222]    [Pg.432]    [Pg.272]    [Pg.687]    [Pg.687]    [Pg.1349]    [Pg.2035]    [Pg.2041]    [Pg.2041]    [Pg.4837]    [Pg.4854]    [Pg.6763]    [Pg.570]    [Pg.1254]   
See also in sourсe #XX -- [ Pg.2 , Pg.3 , Pg.4 , Pg.5 , Pg.6 , Pg.7 , Pg.8 , Pg.9 ]



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