(-)-Linalool

Base Information Edit

Chemical Name:(-)-Linalool
CAS No.:126-91-0
Molecular Formula:C10H18O
Molecular Weight:154.252
Hs Code.:29052230
European Community (EC) Number:204-811-2
UNII:3U21E3V8I2
DSSTox Substance ID:DTXSID40872607
Nikkaji Number:J9.271A
Wikidata:Q27105200
RXCUI:1800669
Metabolomics Workbench ID:28012
ChEMBL ID:CHEMBL235672
Mol file:126-91-0.mol

Synonyms:(-)-Linalool;126-91-0;L-Linalool;(R)-(-)-Linalool;(R)-3,7-dimethylocta-1,6-dien-3-ol;(3R)-Linalool;Licareol;1,6-Octadien-3-ol, 3,7-dimethyl-, (3R)-;Linalool, (-)-;(3R)-3,7-dimethylocta-1,6-dien-3-ol;(R)-3,7-Dimethyl-1,6-octadien-3-ol;LEVO-LINALOOL;3U21E3V8I2;LINALOOL, L-;CHEBI:28;LINALOOL R-(-)-FORM;UNII-3U21E3V8I2;LINALOOL (+);DTXSID40872607;(R)-linalool;EINECS 204-811-2;3R,7-dimethylocta-1,6-dien-3-ol;(R)-(-)-3,7-Dimethyl-1,6-octadien-3-ol;laevo-linalool;(-)-3,7-dimethyl-1,6-octadien-3-ol;(3R)-3,7-dimethyl-1,6-octadien-3-ol;MFCD00135469;Spectrum_000212;SpecPlus_000909;Spectrum2_001944;Spectrum3_001173;Spectrum4_001777;Spectrum5_000393;1,6-OCTADIEN-3-OL, 3,7-DIMETHYL-, (-)-;BSPBio_002785;KBioGR_002294;KBioSS_000692;DivK1c_007005;SCHEMBL891312;SPECTRUM1501212;SPBio_002007;CHEMBL235672;KBio1_001949;KBio2_000692;KBio2_003260;KBio2_005828;KBio3_002285;DTXCID40820244;(-)-Linalool, analytical standard;CCG-38497;L-Linalool, natural, >=95%, FG;LINALOOL R-(-)-FORM [MI];AKOS028109218;LMPR0102010013;SDCCGMLS-0066889.P001;SMP2_000331;NCGC00095658-01;NCGC00095658-02;BS-20066;1,6-Octadien-3-ol, 3,7-dimethyl-, (R)-;J-005448;(-)-Linalool, >=95.0% (sum of enantiomers, GC);Q27105200;(R) - 3,7 - dimethyl - 1,6 - octadien - 3 - ol

Suppliers and Price of (-)-Linalool

Supply Marketing:Edit

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Sigma-Aldrich
(?)-Linalool ≥95.0% (sum of enantiomers, GC)
25ml
$ 52.70

Sigma-Aldrich
L-Linalool natural,≥95%,FG
1 SAMPLE-K
$ 50.00

Sigma-Aldrich
L-Linalool natural, ≥95%, FG
sample-k
$ 50.00

Sigma-Aldrich
L-Linalool natural, ≥95%, FG
1 kg
$ 137.00

Sigma-Aldrich
L-Linalool natural, ≥95%, FG
1kg-k
$ 133.00

Sigma-Aldrich
(?)-Linalool ≥95.0% (sum of enantiomers, GC)
100ml
$ 123.00

Sigma-Aldrich
(?)-Linalool analyticalstandard
1 mL
$ 84.30

Sigma-Aldrich
(?)-Linalool analytical standard
1ml-f
$ 81.70

Sigma-Aldrich
L-Linalool natural, ≥95%, FG
9 kg
$ 1020.00

Sigma-Aldrich
L-Linalool natural, ≥95%, FG
9kg-k
$ 991.00

Total 40 raw suppliers

Chemical Property of (-)-Linalool Edit

Chemical Property:

Appearance/Colour:clear colorless to pale yellow liquid
Vapor Pressure:0.17 mm Hg ( 25 °C)
Refractive Index:n20/D 1.462(lit.)
Boiling Point:198.499 °C at 760 mmHg
PKA:14.51±0.29(Predicted)
Flash Point:84.867 °C
PSA：20.23000
Density:0.859 g/cm³
LogP:2.66980
XLogP3:2.7
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:4
Exact Mass:154.135765193
Heavy Atom Count:11
Complexity:154

Purity/Quality:

99.9% ^*data from raw suppliers

(?)-Linalool ≥95.0% (sum of enantiomers, GC) ^*data from reagent suppliers

Safty Information:

Pictogram(s): C, Xi
Hazard Codes:C,Xi
Statements: 36/37/38-34
Safety Statements: 26-36/37/39-45-36-36/37

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(=CCCC(C)(C=C)O)C
Isomeric SMILES:CC(=CCC[C@](C)(C=C)O)C
Uses (-)-Linalool can be used as a reactant in: The enantioselective preparation of ophiobolin sesterterpene via diastereoselective reductive radical cascade cyclization. The total synthesis of (-)-5,6-dihydrocineromycin B via (-)-linalool O-triethylsilyl ether.; The total synthesis of pladienolide B analog. (-)-Linalool has also been used as a reference standard in the quantitative determination of lavender oil in lavaflam tablets using gas chromatography method of analysis(GC).

Technology Process of (-)-Linalool

There total 63 articles about (-)-Linalool which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 97.0%

: 121401-06-7
Toluene-4-sulfonic acid <3-methyl-3-(4-methylpent-3-enyl)oxiran-2-yl>methyl ester

: 126-91-0
linalool

: 126-90-9
(S)-(+)-linalool

Guidance literature:: With sodium hydroxide; tellurium; rongalite; In tetrahydrofuran; water; at 50 - 55 ℃; for 3h; Title compound not separated from byproducts;
DOI:10.1016/S0040-4039(00)77252-2