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Phenylpropyl alcohol

The results of intrinsic viscosity measurements for four polymer-solvent systems made at the -temperature of each are shown in Fig. 141. The four systems and their -temperatures are polyisobutylene in benzene at 24°C, polystyrene in cyclohexane at 34°C, poly-(di-methylsiloxane) in methyl ethyl ketone at 20°C, and cellulose tricapry-late in 7-phenylpropyl alcohol at 48°C. In each case a series of poly-... [Pg.613]

Fig. 141.—Double logarithmic plot of [77]0 against M for several polymer series polyisobutylene in benzene at 24°C, O polystyrene in cyclohexane at 34°C, cellulose tricaprylate in T-phenylpropyl alcohol at 48 C, Q and... Fig. 141.—Double logarithmic plot of [77]0 against M for several polymer series polyisobutylene in benzene at 24°C, O polystyrene in cyclohexane at 34°C, cellulose tricaprylate in T-phenylpropyl alcohol at 48 C, Q and...
Phenyl-2-propenoic acid, e279 3-Phenyl-2-propen-l-ol, c282 3-Phenyl-2-propenoyl chloride, c280 3-Phenylpropyl alcohol, pi46 Phenyl propyl ketone, b619... [Pg.299]

Typical procedure A solution of trimethyl phosphite (0.85 mmol), 3-phenylpropyl alcohol (0.72 mmol) and lutidine (0.99 mmol) in CH2CI2 (4 mL) was treated with TeCl4 (0.57 mmol) for 1 h at room temperature. Filtration of the black precipitate and chromatography on silica gel afforded dimethy 3-phenylpropyl phosphate (96% yield). [Pg.171]

Cinnamomum aromaticum Nees. C. cassia Presl. Gui Zhi (Cinnamon) (twig, bark) Cinnamic aldehyde, cinnamyl acetate, cinnamic acid, eugenol, phellandrene, phenylpropyl alcohol, coumarin, cinnamic aldehyde, orthomethylcoumaric aldehyde.33-49-254-435-510 Antibacterial, vasodilatation, aromatic stomachic, astringent, tonic, analgesic, stimulate human lymphocytes to proliferate. [Pg.53]

Hexyl cinnamic aldehyde Amyl cinnamic aldehyde Linalyl cinnamate Cinnamic alcohol Cinnamyl acetate Phenylpropyl alcohol Phenylpropyl acetate... [Pg.42]

Cinnamic alcohol Phenylpropyl alcohol Cinnamyl acetate Methyl cinnamate Amyl cinnamic aldehyde Hexyl cinnamic aldehyde... [Pg.46]

Phenylpropyl alcohol Styrax Amyl cinnamic aldehyde... [Pg.48]

A conventional jasmin base again provides the main floral aspect of the perfume. In more modem versions, for example, as in the Eau de Toilette, Lyral is used to replace part or all of the hydroxycitronellal. The styrax note may be reinforced by the use of phenylpropyl alcohol, one of its major constituents. The base note, in many ways similar to that of Ma Griffe, differs in the very much higher level of patchouli (10%). [Pg.127]

In the cinnamic molecule there is an additional conjugational effect between the double bond in the side chain and the unsaturated benzene ring. The saturated form, phenylpropyl alcohol is again the harsher of the two in character. [Pg.221]

SYNS 3-BENZENEPROPANOL FEMA No. 2885 HYDROCINNAAfYL ALCOHOL (3-HYDROXYPROP-YL)BENZENED 7-PHENYLPROPANOL 3-PHENYL-PROPANOL 3-PHENYL-l-PROPANOL(FCC) PHENYLPROPYL ALCOHOL y-PHENWEPROPYL ALCOHOL S-PHENYLPROPYT ALCOHOL... [Pg.738]

The product was reported by Maga (1975b) as having a phenylpropyl alcohol odor. For Winter et al. (1975a), it imparts a sweet, flowery note remembering heliotropine to a sugar syrup when incorporated at... [Pg.256]

The chemical properties of the alcohol are in accord with the structure assigned to it. It is converted by reduction into phenylpropyl alcohol —... [Pg.479]

PHENYLPROPANOL 3-PHENYLPROPANOL PHENYLPROPYL ALCOHOL Y-PHENYLPROPYL ALCOHOL 3-PHENYLPROPYL... [Pg.166]

Dimethyl-3-phenyl-1 -propanol 0,0-Dimethyl-5-phenylpropyl alcohol 2-Methyl-4-phenyl-2-butanol 2-Methyl-4-phenylbutan-2-ol Phenylethyl dimethyl carbinol 2-(2-Phenylethyl )-2-propanol 4-Phenyl-2-methyl-2-butanol 4-Phenyl-2-methyl-butanol-2 1-Propanol, 1,1-dimethyl-3-phenyl-Classification Aromatic alcohol Empirical CnHieO... [Pg.1447]

Dimethyl-3-phenylpropyl acetate. See,2-Methyl-4-phenyl-2-butyl acetate a,a-Dimethyl-5-phenylpropyl alcohol. See Dimethyl phenethyl carbinol... [Pg.1449]

Y-Phenylpropanol Phenylpropyl alcohol 3-Phenylpropyl alcohol y-Phenylpropyl alcohol ... [Pg.2063]

Phenylpropyl alcohol 1-Propanol, 1-phenyl-Empiiical C9H12O Formula C2H5CH(C6Hs)OH Properties Colorless oily liq., floral fragrance sol. in alcohol m.w. 136.19 dens. 0.994 b.p. 103 C (14 mm) flash pt. 90 C ref. index 1.5200 Toxicology LD50 (oral, mouse) 500 mg/kg, (subcut., mouse) 700 mg/kg mod. toxic by ing. and subcut. routes Precaution Combustible liq. [Pg.3332]

See other pages where Phenylpropyl alcohol is mentioned: [Pg.128]    [Pg.185]    [Pg.288]    [Pg.467]    [Pg.648]    [Pg.387]    [Pg.18]    [Pg.20]    [Pg.20]    [Pg.20]    [Pg.44]    [Pg.150]    [Pg.155]    [Pg.216]    [Pg.337]    [Pg.614]    [Pg.1839]    [Pg.387]    [Pg.652]    [Pg.664]    [Pg.975]    [Pg.980]    [Pg.980]    [Pg.702]    [Pg.652]   
See also in sourсe #XX -- [ Pg.454 ]

See also in sourсe #XX -- [ Pg.614 ]

See also in sourсe #XX -- [ Pg.3 , Pg.166 ]

See also in sourсe #XX -- [ Pg.20 , Pg.36 , Pg.262 , Pg.283 , Pg.362 , Pg.449 , Pg.467 , Pg.647 ]



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2- -3-phenylpropyl

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