≥90% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Room temperature Ships Check lot-specific COA for exact specifications.
SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
Cited in 1 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Description
Linalyl formate is found in the essential oils of rosewood, lemongrass andMurraya koenigiifruits oil.
| Pubchem Sid | 488183433 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/488183433 |
| Sourires canoniques | CC(=CCCC(C)(C=C)OC=O)C |
| IUPAC Name | 3,7-dimethylocta-1,6-dien-3-yl formate |
| InChIKey | JZOCDHMHLGUPFI-UHFFFAOYSA-N |
| INCHI | 1S/C11H18O2/c1-5-11(4,13-9-12)8-6-7-10(2)3/h5,7,9H,1,6,8H2,2-4H3 |
| Isomères SMILES | CC(=CCCC(C)(C=C)OC=O)C |
| Poids moléculaire | 182.26 |
| Reaxy-Rn | 1722875 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1722875&ln= |
Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS →Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA →Full quality attributes and acceptance criteria for this grade.
View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Lipids and lipid-like molecules |
| Classe | Prenol lipids |
| Subclass | Monoterpenoids |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Acyclic monoterpenoids |
| Alternative Parents | Carboxylic acid esters Monocarboxylic acids and derivatives Organic oxides Hydrocarbon derivatives Carbonyl compounds |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Acyclic monoterpenoid - Carboxylic acid ester - Monocarboxylic acid or derivatives - Carboxylic acid derivative - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aliphatic acyclic compound |
| Description | This compound belongs to the class of organic compounds known as acyclic monoterpenoids. These are monoterpenes that do not contain a cycle. |
| External Descriptors | Not available |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Date | Article |
|---|---|---|---|
 D2308256 | Certificate of Analysis | Jan 20, 2026 | L475392 |
| D2308258 | Certificate of Analysis | Jan 20, 2026 | L475392 |
| D2308259 | Certificate of Analysis | Jan 20, 2026 | L475392 |
| D2308261 | Certificate of Analysis | Jan 20, 2026 | L475392 |
| D2308264 | Certificate of Analysis | Jan 20, 2026 | L475392 |
| D2308416 | Certificate of Analysis | Jan 20, 2026 | L475392 |
| D2308257 | Certificate of Analysis | Feb 17, 2023 | L475392 |
| I2406222 | Certificate of Analysis | Feb 17, 2023 | L475392 |
| Indice de réfraction | n20/D 1.455 (lit.) |
|---|---|
| Point d'éclair (°F) | 186.8 °F - closed cup |
| Point d'éclair (°C) | 86 °C - closed cup |
| Point d'ébullition (°C) | 100-103℃/10mmHg (lit.) |
| Poids moléculaire | 182.260 g/mol |
| XLogP3 | 3.300 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 6 |
| Exact Mass | 182.131 Da |
| Monoisotopic Mass | 182.131 Da |
| Topological Polar Surface Area | 26.300 Ų |
| Heavy Atom Count | 13 |
| Formal Charge | 0 |
| Complexity | 202.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 1 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 0 |
| Covalently-Bonded Unit Count | 1 |
| 1. Jiao Yang Lu, Quan Jiang, Jiao Jiao Lei, Ying Xuan He, Wei Tao Huang. (2022) Molecular ‘email’: Electrochemical aptasensing of fish pathogens, molecular information encoding, encryption and hiding applications. ANALYTICA CHIMICA ACTA, [PMID:36257750] [10.1016/j.aca.2022.340483] |
