trans-nerolidol
trans-nerolidol
CAS: 40716-66-3
Molecular Formula: C15H26O
trans-nerolidol - Names and Identifiers
| 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+ |
trans-nerolidol - Physico-chemical Properties
| 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 |
trans-nerolidol - Risk and Safety
| 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 |
trans-nerolidol - Upstream Downstream Industry
trans-nerolidol - Reference
| 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 |
trans-nerolidol - Nature
| 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) |
Last Update：2024-04-10 22:29:15
trans-nerolidol - Production method
1. tobacco: FC,18; Using linalool as raw material, linalool is first converted into geraniol acetone, acetylated into dehydronerolol, and hydrogenated into nerolol.
Last Update：2024-04-10 22:29:15
trans-nerolidol - Security information
| 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). |
Last Update：2024-04-10 22:29:15
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View History
Raw Materials for trans-nerolidol
5-Hepten-1-yne, 6-methyl-
Diphosphoric acid, mono[(2Z,6E)-3,7,11-trimethyl-2,6,10-dodecatrien-1-yl] ester
CIS-TRANS-FARNESOL
GERANYL BROMIDE
Geranylacetone
Diphosphoric acid, mono[(2Z,6E)-3,7,11-trimethyl-2,6,10-dodecatrien-1-yl] ester
CIS-TRANS-FARNESOL
GERANYL BROMIDE
Geranylacetone
Downstream Products for trans-nerolidol