- (-)-LINALOOL
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- $40.00 / 1kg
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2023-09-26
- CAS:126-91-0
- Min. Order: 1kg
- Purity: 0.99
- Supply Ability: 10 tons
- (-)-LINALOOL
-
- $0.00 / 1KG
-
2023-09-06
- CAS:126-91-0
- Min. Order: 1KG
- Purity: 99%
- Supply Ability: 500000kg
- (-)-LINALOOL
-
- $0.00 / 1KG
-
2022-10-14
- CAS:126-91-0
- Min. Order: 1KG
- Purity: 98%
- Supply Ability: 1ton
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| | (-)-LINALOOL Basic information |
| Product Name: | (-)-LINALOOL | | Synonyms: | LINALOOL 925;LINALOOL, DL-;LINALOOL EX-BOIS DE ROSE;LINALOOL EX BOIS DE ROSE OIL;LINALYL ALCOHOL;HO-WOOD OIL;3,7-DIMETHYL-6-OCTADIEN-3-OL;(+/-)-3,7-DIMETHYL-3-HYDROXY-1,6-OCTADIENE | | CAS: | 126-91-0 | | MF: | C10H18O | | MW: | 154.25 | | EINECS: | 204-811-2 | | Product Categories: | | | Mol File: | 126-91-0.mol |  |
| | (-)-LINALOOL Chemical Properties |
| Boiling point | 198 °C(lit.) | | density | 0.87 g/mL at 25 °C(lit.) | | vapor pressure | 0.17 mm Hg ( 25 °C) | | refractive index | n20/D 1.462(lit.) | | Fp | 174 °F | | pka | 14.51±0.29(Predicted) | | form | Liquid | | color | Clear colorless to pale yellow | | Odor | at 100.00 %. fresh floral woody natural deep lavender | | Odor Type | floral | | optical activity | [α]20/D 20±2°, neat | | BRN | 1721487 | | LogP | 2.7 at 25℃ | | CAS DataBase Reference | 126-91-0(CAS DataBase Reference) | | EPA Substance Registry System | 1,6-Octadien-3-ol, 3,7-dimethyl-, (3R)- (126-91-0) |
| Hazard Codes | C,Xi | | Risk Statements | 36/37/38-34 | | Safety Statements | 26-36/37/39-45-36-36/37 | | RIDADR | UN 1760 8/PG 2 | | WGK Germany | 3 | | RTECS | RG5800000 | | HS Code | 29052230 | | Toxicity | mouse,LD50,intravenous,180mg/kg (180mg/kg),U.S. Army Armament Research & Development Command, Chemical Systems Laboratory, NIOSH Exchange Chemicals. Vol. NX#01477, |
| | (-)-LINALOOL Usage And Synthesis |
| Chemical Properties | clear colorless to pale yellow liquid | | Uses | (-)-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). | | 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.
| | Definition | ChEBI: The (R)-enantiomer of linalool. | | General Description | L-Linalool is the key volatile compound of jasmine tea, spruce essential oil and young leaves of Litchi chinensis Sonn. |
| | (-)-LINALOOL Preparation Products And Raw materials |
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