LINALOOL
LINALOOL
CAS NO: 78-70-6
METATAGS;Linalool;78-70-6;3,7-Dimethylocta-1,6-dien-3-ol;allo-Ocimenol;beta-Linalool;3,7-Dimethyl-1,6-octadien-3-ol;Linalol;LINALYL ALCOHOL;(+-)-Linalool;p-Linalool;1,6-Octadien-3-ol, 3,7-dimethyl-;.beta.-Linalool;Linalool (natural);2,6-Dimethyl-2,7-octadien-6-ol;2,6-Dimethylocta-2,7-dien-6-ol;Caswell No. 526A;FEMA Number 2635;NSC 3789;FEMA No. 2635;CCRIS 3726;CCRIS 6557;HSDB 645;EINECS 201-134-4;EINECS 245-083-6;3,7-dimethyl-octa-1,6-dien-3-ol;EPA Pesticide Chemical Code 128838;BRN 1721488;AI3-00942;CHEBI:17580;NSC3789;CDOSHBSSFJOMGT-UHFFFAOYSA-N;MFCD00008906;2,7-Octadien-6-ol, 2,6-dimethyl-;(1)-3,7-Dimethyl-1,6-octadien-3-ol;dl-3,7-Dimethyl-3-hydroxy-1,6-octadiene;DSSTox_CID_5502;DSSTox_RID_77812;DSSTox_GSID_25502;Q-201306;Linanool;(S)-Linalol;1,6-Octadien-3-ol,3,7-Dimethyl-;CAS-78-70-6;22564-99-4;( -)-Linalool;1,6-Octadien-3-ol, 3,7-dimethyl-, (3R)-;Linolool;Phantol;EINECS 204-811-2;Howood Oil;Natural Linalool;Linalool, .beta.;( )-linalool;Linalool ex ho oil;Linalool, 97%;Linalool ex orange oil;3,6-octadien-3-ol;1,6-Octadien-3-ol, 3,7-dimethyl-, (3S)-;2,7-octadiene-6-ol;2,7-dien-6-ol;3,6-dien-3-ol;AC1L1MRY;AC1Q1NVD;AC1Q1NVE;LINOLOOL (D);(.+/-.)-Linalool;1,6-OCTADIEN-3-OL, 3,7-DIMETHYL-, (-)-;ACMC-209pf1;EC 201-134-4;AC1Q2BP3;SCHEMBL20316;(+/-) LINALOOL;Linalool ex bois de rose oil;Linalool, analytical standard;0-01-00-00462 (Beilstein Handbook Reference);KSC377K8J;MLS002152908;CHEMBL25306;LINALOOL, (+-)-;DTXSID7025502;LINALOOL EX BOIS DE ROSE;CTK2H7584;MolPort-001-783-101;BB_NC-0123;HMS2268E18;Linalool, >=97%, FCC, FG;1, 3,7-dimethyl-, (-)-;BB_NC-00123;NSC-3789;WLN: 1U1XQ1&3UY1&1;Tox21_201658;Tox21_303037;AC-551;ANW-37211;BBL027734;SBB012353;STL373777;3,7-Dimethyl-1,6-octadien-3-ol|;AKOS015901617;FCH1115719;LS-1752;MCULE-2407576698;RP21877;RTR-030706;NCGC00091688-01;NCGC00091688-02;NCGC00091688-03;NCGC00091688-04;NCGC00257060-01;NCGC00259207-01;(?)-3,7-Dimethyl-1,6-octadien-3-ol;11024-20-7;AK-50127;AN-15757;AN-22986;BC207603;BT000180;LP067292;LS-97796;OR341488;SC-74998;SMR000112394;ST069326;WLN: 1Y1&U3XQ1&1U1 -,-;DB-062552;KB-179981;TR-030706;(+/-)-3,7-Dimethyl-1,6-octadien-3-ol;DL -3,7-Dimethyl-3-hydroxy-1,6-octadiene;FT-0614785;L0048;1,6-Octadien-3-ol, 3,7-dimethyl-, (R)-;C03985;(+/-)-3,7-Dimethyl-3-hydroxy-1,6-octadiene;Linalool, primary pharmaceutical reference standard;CU-01000013132-2;I14-13929;Linalool, certified reference material, TraceCERT(R)
EC Number: 201-134-4
Molecular Formula of Linalool
C10H18O
(CH3)2C=CH(CH2)2C(CH3)(OH)CH=CH2
Chemical and Physical Properties of Linalool
Property Name
Molecular Weight: 154.253 g/mol
Hydrogen Bond Donor Count: 1
Hydrogen Bond Acceptor Count: 1
Rotatable Bond Count: 4
Complexity: 154
Topological Polar Surface Area: 20.2 A^2
Monoisotopic Mass: 154.136 g/mol
Exact Mass: 154.136 g/mol
XLogP3-AA: 2.7
Compound Is Canonicalized: true
Formal Charge: 0
Heavy Atom Count: 11
Defined Atom Stereocenter Count: 0
Undefined Atom Stereocenter Count: 1
Defined Bond Stereocenter Count: 0
Undefined Bond Stereocenter Count: 0
Isotope Atom Count: 0
Covalently-Bonded Unit Count: 1
Experimental Properties of Linalool
hysical Description of Linalool
DryPowder, Liquid, OtherSolid
Liquid
Color of Linalool
Colorless liquid
Odor of Linalool
Odor similar to that of bergamot oil and French lavender.
Taste of Linalool
Taste characteristics at 30 ppm: Floral, woody, sweet with a green, spicy tropical nuance
Boiling Point of Linalool
198 deg C
Density of Linalool
0.865 at 15 deg C
The lily smell for linalool is not exactly true, but it is a beautiful fragrance molecule that is lily of the valley and is a natural, fragrant natural fragrance, found in many enantiomers in many plants. For example, 60-70% of coriander oil forms (+) – enantiomer of linalool. The racemic mixture is a colorless mixture of lily flavor, like its enantiomers, and a fresh, chic smell. Between the enantiomers there is a slight odor difference. Along with esther states, linalool is one of the most commonly used and fragrant molecules produced in large quantities.
C Numaras: 201-134-4
Linalool’un molekül formülü
C10H18O
(CH3) 2C = CH (CH2) 2C (CH3) (OH) CH = CH2,
Linalool’un kimyasal ve fiziksel özellikleri
Özellik ad
Moleküler Arlk: 154.253 g / mol
Hidrojen Bam Balayc Says: 1
Hidrojen Ba Alc Says: 1
Dönebilen Bond Says: 4
Karmaklk: 154
Topolojik Polar Yüzey Alan: 20.2 A ^ 2
Monoizotopic Kütle: 154.136 g / mol
Tam Kütle: 154.136 g / mol
XLogP3-AA: 2.7
Bileik Canonicalized: true
Resmi arj: 0
Ar Atom Says: 11
Tanml Atom Stereocenter Says: 0
Tanmsz Atom Stereocenter Says: 1
Tanml Bono Stereocenter Says: 0
Tanmlanmam Bond Stereocenter Says: 0
zotop Atom Says: 0
Kovalent Bal Birim Says: 1
Linalool’un Deneysel Özellikleri
Hysical Linalool’un açklamas
Kuru Parca, Sv, DierKat
Sv
Linalool’un rengi
Renksiz sv
Linalool kokusu
Bergamot ya ve Fransz lavanta benzeri koku.
Linalool’un tadna bak
30 ppm’de tat özellikleri: Çiçekli, odunsu, tatl, yeil, baharatl tropikal nüans
Linalool’un Kaynama Noktas
198 derece C
Linalool younluu
0.865, 15 derece C’de
Linalool icin zambak kokusu demek tam dogru olmasa da, bir cok bitkide farkli enantiomerler halinde bulunan, zambak kokusunu andiran, ciceksi dogal bir güzel koku molekülüdür. Örnegin kini yaginin %60-70’ini linalool’un (+)- enantiomeri olusturur. Rasemik karisim hali de enantiomerleri gibi zambak kokusunu andiran, taze, ciceksi bir kokuya sahip olan renksiz bir sividir. Enantiomerleri arasinda cok az da olsa bir koku farki vardir. Ester halleri ile ile birlikte, linalool, en sik kullanilan ve oldukca büyük miktarlarda üretilen güzel koku moleküllerinden biridir.