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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 Numarası: 201-134-4

Linalool'un molekül formülü
C10H18O

(CH3) 2C = CH (CH2) 2C (CH3) (OH) CH = CH2,

Linalool'un kimyasal ve fiziksel özellikleri

Özellik adı
Moleküler Ağırlık: 154.253 g / mol
Hidrojen Bağımı Bağışlayıcı Sayısı: 1
Hidrojen Bağ Alıcı Sayısı: 1
Dönebilen Bond Sayısı: 4
Karmaşıklık: 154
Topolojik Polar Yüzey Alanı: 20.2 A ^ 2
Monoizotopic Kütle: 154.136 g / mol
Tam Kütle: 154.136 g / mol
XLogP3-AA: 2.7
Bileşik Canonicalized: true
Resmi Şarj: 0
Ağır Atom Sayısı: 11
Tanımlı Atom Stereocenter Sayısı: 0
Tanımsız Atom Stereocenter Sayısı: 1
Tanımlı Bono Stereocenter Sayısı: 0
Tanımlanmamış Bond Stereocenter Sayısı: 0
İzotop Atom Sayısı: 0
Kovalent Bağlı Birim Sayısı: 1

Linalool'un Deneysel Özellikleri

Hysical Linalool'un açıklaması
Kuru Parca, Sıvı, DiğerKatı
Sıvı

Linalool'un rengi
Renksiz sıvı

Linalool kokusu
Bergamot yağı ve Fransız lavanta benzeri koku.

Linalool'un tadına bak
30 ppm'de tat özellikleri: Çiçekli, odunsu, tatlı, yeşil, baharatlı tropikal nüans

Linalool'un Kaynama Noktası
198 derece C

Linalool yoğunluğu
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 kişniş 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.

 

 


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.

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