(CH3)2C=CH-(CH2)2-C(OH)(CH3)-CH=CH2 [1 Record] - Termium

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(CH3)2C=CH-(CH2)2-C(OH)(CH3)-CH=CH2 [1 record]

Filter results by subject field Alphabetical list of terms Chemical Elements and Compounds [1]Food Additives [1]Perfume and Cosmetics Industry [1]

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• (CH3)2C:CH(CH2)2CH(CH3)CHO
• (CH3)2C:CHCH2CH2C(CH3)OHCH:CH2
• (CH3)2C=CH-(CH2)2-C(CH3)=CH-CH2OH
• (CH3)2C=CH-(CH2)2-C(OH)(CH3)-CH=CH2
• (CH3)2C=CH-(CH2)2-CH(CH3)-CHO
• (CH3)2CH-CH2-CO-CH3
• (CH3)2CH2O
• (CH3)2CHC6H3(CH3)(OH)
• (CH3)2CHC6H4CHO
• (CH3)2CHCH(CH3)2
• (CH3)2CHCH2C(O)CH3
• (CH3)2CHCH2C(O)H
• (CH3)2CHCH2CH(CH3)OH
• (CH3)2CHCH2CH2OH
• (CH3)2CHCH2CH3
• (CH3)2CHCH2CHOH(CH3)
• (CH3)2CHCH2OH
• (CH3)2CHCH3
• (CH3)2CHCH=CH2
• (CH3)2CHCHO
• (CH3)2CHCOCL
• (CH3)2CHCOOH
• (CH3)2CHNH2
• (CH3)2CHNO3
• (CH3)2CHOC(O)OOC(O)OCH(CH3)2
• (CH3)2CHOCH(CH3)2
• (CH3)2CHOOCC15H31
• (CH3)2CHOOCC3H7
• (CH3)2CHOOCCL
• (CH3)2CNOH
• (CH3)2COH-CBR3
• (CH3)2COHCH2CH2OCH3
• (CH3)2COHCN
• (CH3)2N-C6H4-CO-C6H4-N(CH3)2
• (CH3)2N-NO
• (CH3)2N2O
• (CH3)2NCH2CH2CH2NH2
• (CH3)2NCS2NH4
• (CH3)2NH
• (CH3)2NNO
• (CH3)2SE

• Chemical Elements and Compounds
• Food Additives
• Perfume and Cosmetics Industry

(CH3)2C:CHCH2CH2C(CH3)OHCH:CH2 8, record 1, English, %28CH3%292C%3ACHCH2CH2C%28CH3%29OHCH%3ACH2 formula, see observation(CH3)2C=CH-(CH2)2-C(OH)(CH3)-CH=CH2 9, record 1, English, %28CH3%292C%3DCH%2D%28CH2%292%2DC%28OH%29%28CH3%29%2DCH%3DCH2 formula, see observationC10H17OH 10, record 1, English, C10H17OH formula, see observationC10H18O 11, record 1, English, C10H18O formula, see observation78-70-6 12, record 1, English, 78%2D70%2D6 CAS number

Record 1, Main entry term, English

• 3,7-dimethylocta-1,6-dien-3-ol 1, record 1, English, 3%2C7%2Ddimethylocta%2D1%2C6%2Ddien%2D3%2Dol correct, see observation

Record 1, Abbreviations, English

Record 1, Synonyms, English

• linalool 2, record 1, English, linalool correct
• ß-linalool 3, record 1, English, %C3%9F%2Dlinalool correct
• 3,7-dimethyl-1,6-octadien-3-ol 4, record 1, English, 3%2C7%2Ddimethyl%2D1%2C6%2Doctadien%2D3%2Dol former designation
• linalol 5, record 1, English, linalol former designation
• linalyl alcohol 1, record 1, English, linalyl%20alcohol former designation

Record 1, Textual support, English

Record number: 1, Textual support number: 1 DEF

A fragrant liquid unsaturated optically active unsaturated tertiary alcohol which occurs both free and in the form of esters in many essential oils, especially linaloe oils, and which is used in perfumes, soaps and flavoring materials. 6, record 1, English, - 3%2C7%2Ddimethylocta%2D1%2C6%2Ddien%2D3%2Dol

Record number: 1, Textual support number: 1 OBS

Linalool exists under three forms: racemic: «dl» or «(±)» or «rac»; dextrogyre: «d» or «(+)»; and levogyre: «l» or «(-)». The prefixes «dl», «d» and «l» must be italicized. It is to be noted that the stereodescriptors (±), (+) and (-) are nowadays preferred. See also the records for the related concepts "coriandrol" and "licareol." 3, record 1, English, - 3%2C7%2Ddimethylocta%2D1%2C6%2Ddien%2D3%2Dol

Record number: 1, Textual support number: 2 OBS

In the dextrorotatory form it is obtained especially from bois de rose oil or coriander oil, in levorotatory form from Mexican linaloe oil and the oil froma Japanese cinnamon, and in racemic form by isomerication of geraniol or synthetically. All optically isomeric and all used in perfumes, soaps, and flavoring materials. 7, record 1, English, - 3%2C7%2Ddimethylocta%2D1%2C6%2Ddien%2D3%2Dol

Record number: 1, Textual support number: 3 OBS

3,7-dimethylocta-1,6-dien-3-ol: form recommended by the IUPAC (International Union of Pure and Applied Chemistry). 3, record 1, English, - 3%2C7%2Ddimethylocta%2D1%2C6%2Ddien%2D3%2Dol

Record number: 1, Textual support number: 4 OBS

Chemical formula: (CH3)2C:CHCH2CH2C(CH3)OHCH:CH2 or (CH3)[subscript 2C=CH-(CH2)[subscript 2-C(OH)(CH3)-CH=CH2 or C10H17OH or C10H18O 6, record 1, English, - 3%2C7%2Ddimethylocta%2D1%2C6%2Ddien%2D3%2Dol

• beta-linalool

• Éléments et composés chimiques
• Additifs alimentaires
• Parfumerie

(CH3)2C:CHCH2CH2C(CH3)OHCH:CH2 6, record 1, French, %28CH3%292C%3ACHCH2CH2C%28CH3%29OHCH%3ACH2 formula, see observation(CH3)2C=CH-(CH2)2-C(OH)(CH3)-CH=CH2 7, record 1, French, %28CH3%292C%3DCH%2D%28CH2%292%2DC%28OH%29%28CH3%29%2DCH%3DCH2 formula, see observationC10H17OH 8, record 1, French, C10H17OH formula, see observationC10H18O 3, record 1, French, C10H18O formula, see observation78-70-6 9, record 1, French, 78%2D70%2D6 CAS number

Record 1, Main entry term, French

• 3,7-diméthylocta-1,6-dién-3-oil 1, record 1, French, 3%2C7%2Ddim%C3%A9thylocta%2D1%2C6%2Ddi%C3%A9n%2D3%2Doil correct, see observation, masculine noun

Record 1, Abbreviations, French

Record 1, Synonyms, French

• linalol 2, record 1, French, linalol correct, masculine noun
• ß-linalol 1, record 1, French, %C3%9F%2Dlinalol correct, masculine noun
• diméthyl-3,7 octadiène-1,6 ol-3 3, record 1, French, dim%C3%A9thyl%2D3%2C7%20octadi%C3%A8ne%2D1%2C6%20ol%2D3 former designation, correct, masculine noun
• alcool linalylique 1, record 1, French, alcool%20linalylique former designation, masculine noun

Record 1, Textual support, French

Record number: 1, Textual support number: 1 DEF

Alcool terpénique utilisé dans les savons, en parfumerie, et comme aromatisant. 4, record 1, French, - 3%2C7%2Ddim%C3%A9thylocta%2D1%2C6%2Ddi%C3%A9n%2D3%2Doil

Record number: 1, Textual support number: 1 OBS

Le linalol existe sous trois formes : «dl» ou «(±)» ou «rac», qui indique la forme racémique; «d» ou «(+)», qui indique la forme dextrogyre; et «l» ou «(-)», qui indique la forme lévogyre. Les préfixes «dl», «d» et «l» s'écrivent en italique. Il est cependant à noter qu'on préfère aujourd'hui les stéréodescripteurs (±), (+) et (-). Voir aussi les fiches pour les notions apparentées «coriandrol» et «licaréol». 1, record 1, French, - 3%2C7%2Ddim%C3%A9thylocta%2D1%2C6%2Ddi%C3%A9n%2D3%2Doil

Record number: 1, Textual support number: 2 OBS

L'antipode lévogyre du linalol se rencontre dans les essences de linaloé, de bergamote et de lavande; l'antipode dextrogyre, dans les essences de coriandre, de mandarine et d'orange. Son odeur suave de lavande le fait employer en parfumerie. Le composé racémique se prépare aisément par synthèse et sert à la synthèse industrielle des ionones et de la vitamine A. Les acides cyclisent le linalol en terpinéol et terpine. 5, record 1, French, - 3%2C7%2Ddim%C3%A9thylocta%2D1%2C6%2Ddi%C3%A9n%2D3%2Doil

Record number: 1, Textual support number: 3 OBS

3,7-diméthylocta-1,6-dién-3-ol : forme recommandée par l'UICPA (Union internationale de chimie pure et appliquée). 1, record 1, French, - 3%2C7%2Ddim%C3%A9thylocta%2D1%2C6%2Ddi%C3%A9n%2D3%2Doil

Record number: 1, Textual support number: 4 OBS

Formule chimique : (CH3)2C:CHCH2CH2C(CH3)OHCH:CH2 ou (CH3)[indice 2C=CH-(CH2)[indice 2-C(OH)(CH3)-CH=CH2 ou C10H17OH ou C10H18O, 4, record 1, French, - 3%2C7%2Ddim%C3%A9thylocta%2D1%2C6%2Ddi%C3%A9n%2D3%2Doil

• bêta-linalol

Record 1, Textual support, Spanish

Save record 1

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