|
| 3,7-Dimethyl-2,6-octadienenitrile Basic information |
Product Name: | 3,7-Dimethyl-2,6-octadienenitrile | Synonyms: | 3,7-DIMETHYL-OCTA-2,6-DIENENITRILE;3,7-DIMETHYL-2,6-OCTADIENENITRILE;3,7-DIMETHYL-2,6-OCTADIENE-1-NITRILE;2,6-DIMETHYL-1,5-HEPTADIENYL CYANIDE;LRT8;CITRALVA;GERANONITRILE;GERANYL NITRILE | CAS: | 5146-66-7 | MF: | C10H15N | MW: | 149.23 | EINECS: | 225-918-0 | Product Categories: | Acyclic Monoterpenes;Biochemistry;Terpenes;Alphabetical Listings;C-D;Flavors and Fragrances;C10 to C27;Cyanides/Nitriles;Nitrogen Compounds | Mol File: | 5146-66-7.mol | |
| 3,7-Dimethyl-2,6-octadienenitrile Chemical Properties |
Boiling point | 110 °C1.3 mm Hg(lit.) | density | 0.853 g/mL at 25 °C(lit.) | vapor pressure | 3.7-4.82Pa at 20-25℃ | refractive index | n20/D 1.475(lit.) | Fp | >230 °F | storage temp. | Sealed in dry,Room Temperature | form | clear liquid | Specific Gravity | 0.866 | color | A colourless or very pale yellow liquid. | Odor | at 10.00 % in dipropylene glycol. citrus lemon nitrile aldehydic metallic | Odor Type | citrus | Water Solubility | SLIGHTLY SOLUBLE | LogP | 2.7-3.47 at 35℃ | CAS DataBase Reference | 5146-66-7(CAS DataBase Reference) | EPA Substance Registry System | 2,6-Octadienenitrile, 3,7-dimethyl- (5146-66-7) |
Hazard Codes | Xn,N | Risk Statements | 51/53-68-20/21 | Safety Statements | 36/37-61-23 | RIDADR | UN 3082 9/PG 3 | WGK Germany | 1 | RTECS | RG5370000 | HS Code | 29269095 | toxicity | The acute oral LD50 value in rats was reported as 31 g/kg and the acute dermal LD50 value in rabbits as 4.3 g/kg (Wohl. 1974). |
| 3,7-Dimethyl-2,6-octadienenitrile Usage And Synthesis |
Chemical Properties | CLEAR YELLOW LIQUID | Occurrence | Has apparently not been reported to occur in nature. | Uses | Geranyl Nitrite, is a substituted terpenoid odorant with a fruity odor quality. It is one of the most potent cyclase stimulators. | Preparation | From geranialoxime with acetic anhydride (Arctander. 1969). | Flammability and Explosibility | Nonflammable | Metabolism | The toxicity of organic cyanides appears to depend, in almost every case, on whether they can be metabolized in the body to the free cyanide ion, CN~, and on the rate and extent of this conversion and the rate of detoxication of cyanide to thiocyanate. Alkyl cyanides appear to be metabolized in the body chiefly by formation of hydrogen cyanide plus the acid with one less carbon atom (Williams, 1959). |
| 3,7-Dimethyl-2,6-octadienenitrile Preparation Products And Raw materials |
|