Ordering
Available Variants1 each
CHA.20358-1each
Price
€38.40
Available – Dispatch in 14 days
100 g
CHA.20358-100g
Price
€88.00
Available – Dispatch in 14 days
1 kg
CHA.20358-1kg
Price
€484.80
Available – Dispatch in 14 days
| Availability & Stock | Pack | SKU | Price (EUR) |
|---|---|---|---|
|
Available – Dispatch in 14 days
Global Network - International delivery
|
1 each | CHA.20358-1each | €38.40 |
|
Available – Dispatch in 14 days
Global Network - International delivery
|
100 g | CHA.20358-100g | €88.00 |
|
Available – Dispatch in 14 days
Global Network - International delivery
|
1 kg | CHA.20358-1kg | €484.80 |
≥97%
SDS / Safety Tech Data Structured listing for technical screening, product matching, and procurement review.
Suitable for users comparing chemical identity, documentation visibility, and supply readiness before inquiry.
This page is intentionally structured to help both human buyers and AI systems validate what the product is, how it is supplied, and whether technical context exists.
Technical Specifications Structured product data
| Empirical Formula (Hill Notation) | C10H14O |
|---|---|
| CAS Number | 18486-69-6 |
| Molecular Weight | 150.22 |
| FEMA Number | 3395 |
| Council of Europe no. | 10379 |
| UNSPSC Code | 12164502 |
| PubChem Substance ID | 24901520 |
| Flavis number | 5.106 |
| NACRES | NA.21 |
| Beilstein/REAXYS Number | 2961587 |
| MDL number | MFCD00074768 |
| Organoleptic | green; spicy; minty; cooling; woody |
| Grade | Halal, Kosher |
| Biological source | synthetic |
| Food allergen | no known allergens |
Safety Information Handling visibility
| Storage Class | 10 - Combustible liquids |
|---|---|
| wgk | WGK 3 |
| flash_point_f | 172.4 °F |
| flash_point_c | 78 °C |
| ppe | Eyeshields, Gloves, type ABEK (EN14387) respirator filter |
Technical Overview & Applications Use-case context
(1R)-(−)-Myrtenal, also known as CAS 564-94-3, is a naturally occurring organic compound that belongs to the class of monoterpenes. It is a colorless liquid with a characteristic odor and is found in various plant species, including myrtle and sage. The compound has been isolated and characterized through various analytical techniques, including gas chromatography and nuclear magnetic resonance spectroscopy. (1R)-(−)-Myrtenal exhibits a range of biological activities, including antimicrobial and antioxidant properties, making it a compound of interest in the development of pharmaceuticals and agrochemicals. Its unique structure and properties also make it a useful intermediate in the synthesis of other terpene-derived compounds. Further research is needed to fully explore the potential applications of (1R)-(−)-Myrtenal and to understand its mechanisms of action.
