Customization: | Available |
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CAS No.: | 6259-76-3 |
Formula: | C13h18o3 |
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Hexyl salicylate Chemical Properties |
Boiling point | 290 °C (lit.) |
density | 1.04 g/mL at 25 °C (lit.) |
refractive index | n20/D 1.505(lit.) |
Fp | >230 °F |
storage temp. | Sealed in dry,Room Temperature |
pka | 8.17±0.30(Predicted) |
form | neat |
color | Colourless oily liquid. |
Water Solubility | 0.28g/L(37 ºC) |
BRN | 2453103 |
CAS DataBase Reference | 6259-76-3(CAS DataBase Reference) |
NIST Chemistry Reference | N-hexyl salicylate(6259-76-3) |
EPA Substance Registry System | Hexyl salicylate (6259-76-3) |
Safety Information |
Hazard Codes | Xi |
Risk Statements | 36/37/38 |
Safety Statements | 26-36 |
RIDADR | UN 3082 9 / PGIII |
WGK Germany | 2 |
RTECS | DH2207000 |
toxicity | Both the acute oral LD50 value in rats and the acute dermal LD50 value in rabbits exceeded 5 g/kg (Moreno, 1975). |
Hexyl salicylate Usage And Synthesis |
Chemical Properties | Colorless and transparent oil liquid |
Chemical Properties | Hexyl Salicylate has been reported in carnation flower absolute . It is a colorless liquid with a green, floral, spicy odor, reminiscent of azaleas. It is used for blossom and herbal notes in perfumes, for example, in soaps, personal hygiene products, and detergents. |
Occurrence | Has apparently not been reported to occur in nature. |
Preparation | By methyl salicylate exchange with n-hexanol using a sodium methoxylate catalyst. |
Metabolism | Because of the widespread medicinal use of salicyclic acid and its derivatives, there is an extensive literature on the metabolism and excretion of these compounds. Most esters of salicyclic acid hydrolyse to salicylic acid in the body, but this occurs more readily with the lower esters, little of the amyl ester being split. A large proportion of salicylic acid is excreted unchanged by most species; salicyluric acid, gentisic acid, and salicylglucuronides are also known to be excreted (Williams. 1959). Salicylic acid has been found to be teratogenic to rats (Koshakji. 1972). |