- (E)-2-Octenal
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- $34.00 / 1kg
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2025-09-25
- CAS:2548-87-0
- Min. Order: 1kg
- Purity: 99%
- Supply Ability: g-kg-tons, free sample is available
- (E)-2-Octenal
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- $0.00 / 1kg
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2025-09-05
- CAS:2548-87-0
- Min. Order: 1kg
- Purity: 95%
- Supply Ability: 1
- (E)-2-Octenal
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- $30.00 / 1KG
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2025-06-27
- CAS:2548-87-0
- Min. Order: 50KG
- Purity: 99%
- Supply Ability: 500000kg
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| | (E)-2-Octenal Basic information |
| | (E)-2-Octenal Chemical Properties |
| Melting point | 3.5°C (estimate) | | Boiling point | 84-86 °C19 mm Hg(lit.) | | density | 0.846 g/mL at 25 °C(lit.) | | vapor density | >1 (vs air) | | FEMA | 3215 | 2-OCTENAL | | refractive index | n20/D 1.45(lit.) | | Fp | 150 °F | | storage temp. | 2-8°C | | solubility | Chloroform (Soluble), Methanol (Slightly) | | form | liquid | | color | Colourless | | Odor | at 1.00 % in dipropylene glycol. fresh cucumber fatty green herbal banana waxy green leaf | | Odor Type | fatty | | biological source | synthetic | | Water Solubility | Not miscible or difficult to mix in water. Soluble in alcohol and fixed oils. | | Sensitive | Air Sensitive | | JECFA Number | 1363 | | Henry's Law Constant | 1.3×10-1 mol/(m3Pa) at 25℃, Buttery et al. (1971) | | Stability: | Air Sensitive, Light Sensitive | | Cosmetics Ingredients Functions | PERFUMING | | InChI | 1S/C8H14O/c1-2-3-4-5-6-7-8-9/h6-8H,2-5H2,1H3/b7-6+ | | InChIKey | LVBXEMGDVWVTGY-VOTSOKGWSA-N | | SMILES | [H]C(=O)C(\[H])=C(/[H])CCCCC | | LogP | 2.64 | | CAS DataBase Reference | 2548-87-0(CAS DataBase Reference) | | NIST Chemistry Reference | 2-Octenal, (E)-(2548-87-0) | | EPA Substance Registry System | 2-Octenal, (2E)- (2548-87-0) |
| Hazard Codes | Xi | | Risk Statements | 36/37/38 | | Safety Statements | 26-36/37/39 | | WGK Germany | 3 | | RTECS | RH2130000 | | TSCA | TSCA listed | | HS Code | 29121900 | | Storage Class | 10 - Combustible liquids | | Hazard Classifications | Eye Irrit. 2
Skin Irrit. 2
STOT SE 3 | | Toxicity | dnd-ham-fbr 250 mmol/l/1H MUREAV 497,185,2001 |
| | (E)-2-Octenal Usage And Synthesis |
| Chemical Properties | Colorless liquid | | Uses | trans-2-Octenal is one of the probable major contributors to the Californian long-grain cooked rice odor. | | Definition | ChEBI: The (E)-isomer of oct-2-enal. | | Synthesis Reference(s) | The Journal of Organic Chemistry, 51, p. 2607, 1986 DOI: 10.1021/jo00363a043
Journal of the American Chemical Society, 93, p. 1724, 1971 DOI: 10.1021/ja00736a027
Tetrahedron, 39, p. 3207, 1983 DOI: 10.1016/S0040-4020(01)91568-6 | | General Description | The rate constant for the gas-phase reaction of the NO(3) radical with trans-2-octenal was studied using absolute rate method. The fungal volatile organic compound trans-2-octenal, caused locomotory defects and changes in green fluorescent protein (GFP) and antigen-labeled dopaminergic neurons in adult Drosophila melanogaster. | | Safety Profile | Mutation data reported. Whenheated to decomposition it emits acrid smoke andirritating vapors. |
| | (E)-2-Octenal Preparation Products And Raw materials |
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