Name | trans-nerolidol |
Synonyms | Nerolidol trans-nerolidol Trans-(E)-Nerolidol Teprenone Impurity 19 trans-Nerolidal solution (E)-3,7,11-trimethyldodeca-1,6,10-trien-3-ol (6E)-3,7,11-Trimethyl-1,6,10-dodecatrien-3-ol 3-Hydroxy-3,7,11-trimethyl-1,6,10-dodecatriene 1,6,10-Dodecatrien-3-ol, 3,7,11-trimethyl-, (E)- |
CAS | 40716-66-3 |
EINECS | 255-053-4 |
InChI | InChI=1/C15H26O/c1-6-15(5,16)12-8-11-14(4)10-7-9-13(2)3/h6,9,11,16H,1,7-8,10,12H2,2-5H3/b14-11+ |
Molecular Formula | C15H26O |
Molar Mass | 222.4 |
Density | 0.875 |
Boling Point | 114℃ (1 mmHg) |
Flash Point | 96℃ |
Appearance | Oil |
Storage Condition | 2-8℃ |
Refractive Index | 1.479 |
Hazard Symbols | Xi - Irritant |
Risk Codes | R36/37/38 - Irritating to eyes, respiratory system and skin. |
Safety Description | S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S36 - Wear suitable protective clothing. |
UN IDs | UN1230 - class 3 - PG 2 - Methanol, solution |
Reference Show more | 1. [IF=4.35] Yao Ma et al."Volatile Oil Profile of Prickly Ash (Zanthoxylum) Pericarps from Different Locations in China."Foods. 2021 Oct;10(10):2386 2. [IF=2.633] Ruoke Ma et al."Variation of Chemical Components in Sapwood, Transition Zone, and Heartwood of Dalbergia odorifera and Its Relationship with Heartwood Formation."Forests. 2021 May;12(5):577 |
storage conditions | -20°C |
acidity coefficient (pKa) | 14.40±0.29(Predicted) |
morphology | neat |
JECFA Number | 1646 |
Merck | 13,6501 |
BRN | 5731231 |
NIST chemical information | 1,6,10-Dodecatrien-3-ol, 3,7,11-trimethyl-, (e)-(40716-66-3) |
1. tobacco: FC,18; Using linalool as raw material, linalool is first converted into geraniol acetone, acetylated into dehydronerolol, and hydrogenated into nerolol.
WGK Germany | 1 |
F | 10-23 |
Toxicity | Both the acute oral LD50 in rats and the acute dermal LD50 in rabbits exceeded 5 g/kg (Russell. 1973). |