- Nopol
-
-
2026-06-30
- CAS:128-50-7
- Min. Order: 1kg
- Purity: 98%
- Supply Ability: 1000kg
- Nopol
-
- $1980.00
-
2026-05-11
- CAS:128-50-7
- Purity:
- Supply Ability: 10g
|
| Product Name: | NOPOL | | Synonyms: | NOPOL;2-(6,6-Dimethylbicyclo[3.1.1]hept-2-en-2-yl)ethanol;6,6-Dimethyl-2-(2-hydroxyethyl)-2-norpinene;6,6-dimethyl-2-norpinene-2-ethano;6,6-Dimethylbicyclo-(3.1.1)-2-heptene-2-ethanol;6,6-dimethyl-bicyclo[3.1.1]hept-2-ene-2-ethano;Bicyclo[3.1.1]hept-2-ene-2-ethanol, 6,6-dimethyl-;Homomyretenol | | CAS: | 128-50-7 | | MF: | C11H18O | | MW: | 166.26 | | EINECS: | 204-890-3 | | Product Categories: | | | Mol File: | 128-50-7.mol |  |
| | NOPOL Chemical Properties |
| Boiling point | 230-240 °C | | density | 0.973 | | FEMA | 3938 | 10-HYDROXYMETHYLENE-2-PINENE | | refractive index | 1.492-1.494 | | Fp | 98 °C | | pka | 15.03±0.10(Predicted) | | Odor | at 100.00 %. sweet balsamic citrus pine herbal | | Odor Type | balsamic | | JECFA Number | 986 | | Major Application | flavors and fragrances | | Cosmetics Ingredients Functions | PERFUMING | | InChI | 1S/C11H18O/c1-11(2)9-4-3-8(5-6-12)10(11)7-9/h3,9-10,12H,4-7H2,1-2H3 | | InChIKey | ROKSAUSPJGWCSM-UHFFFAOYSA-N | | SMILES | OCCC1=CCC2CC1C2(C)C | | LogP | 3.09 | | EPA Substance Registry System | Bicyclo[3.1.1]hept-2-ene-2-ethanol, 6,6-dimethyl- (128-50-7) |
| Hazard Codes | Xn | | Risk Statements | 22 | | WGK Germany | WGK 3 | | TSCA | TSCA listed | | Storage Class | 10 - Combustible liquids | | Hazard Classifications | Acute Tox. 4 Oral | | Toxicity | mouse,LD50,intramuscular,500mg/kg (500mg/kg),Journal of Scientific and Industrial Research, Section C: Biological Sciences. Vol. 21, Pg. 342, 1962. |
| Provider | Language |
|
ACROS
| English |
| | NOPOL Usage And Synthesis |
| Chemical Properties | 10-Hydroxymethylene-2-pinene has a mild, woody, camphoraceous odor. | | Occurrence | Reported found in carrots | | Uses |
Nopol is by and large confined to woody and piney fragrance types, in which it may be the chief ingredient or "carrier". But its own odor contribution is very limited, and the title material will ruin almost any floral note if the Nopol is used at higher levels of concentration.
| | Preparation |
Nopol is produced by condensation of beta-Pinene with Formaldehyde under pressure (= at elevated temperature).
|
| | NOPOL Preparation Products And Raw materials |
|