- 1'-Acetonaphthone
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- $45.00 / 1kg
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2024-12-20
- CAS:941-98-0
- Min. Order: 1kg
- Purity: 99%
- Supply Ability: 20 tons
- 1'-Acetonaphthone
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- $0.00 / 1KG
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2024-10-26
- CAS:941-98-0
- Min. Order: 1KG
- Purity: 99%
- Supply Ability: 500000kg
- 1'-Acetonaphthone
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- $10.70 / 1KG
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2024-10-11
- CAS:941-98-0
- Min. Order: 10KG
- Purity: 99%
- Supply Ability: 10000kg
Related articles - What is 1'-Acetonaphthone?
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- Jan 16，2020
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| | 1'-Acetonaphthone Basic information |
| | 1'-Acetonaphthone Chemical Properties |
| Melting point | 10.5 °C (lit.) | | Boiling point | 302 °C (lit.) | | density | 1.12 g/mL at 25 °C (lit.) | | vapor pressure | 0.052Pa at 25℃ | | refractive index | n20/D 1.628(lit.) | | Fp | >230 °F | | storage temp. | Sealed in dry,Room Temperature | | solubility | 0.2g/l | | form | powder | | color | Clear pale yellow to yellow | | PH | 6.5-7.0 (H2O) | | Odor | at 10.00 % in dipropylene glycol. sweet neroli orange blossom powdery | | Odor Type | floral | | Water Solubility | immiscible | | BRN | 1100618 | | Dielectric constant | 4.5（Ambient） | | Exposure limits | ACGIH: TWA 1 mg/m3
OSHA: TWA 15 mg/m3; TWA 5 mg/m3 | | LogP | 3.368 at 25℃ | | CAS DataBase Reference | 941-98-0(CAS DataBase Reference) | | NIST Chemistry Reference | Ethanone, 1-(1-naphthalenyl)-(941-98-0) | | EPA Substance Registry System | Ethanone, 1-(1-naphthalenyl)- (941-98-0) |
| Hazard Codes | Xi,Xn | | Risk Statements | 36/37/38-22 | | Safety Statements | 26-36 | | WGK Germany | - | | RTECS | BD1200000 | | F | 3 | | Hazard Note | Irritant | | TSCA | Yes | | HS Code | 29143900 | | Toxicity | LD50 orl-rat: 1560 mg/kg FCTOD7 20,755,82 |
| | 1'-Acetonaphthone Usage And Synthesis |
| Chemical Properties | clear pale yellow to yellow liquid | | Uses | Used as an abrasive, catalyst, absorbent in petroleum industry, filler for coatings, food additive, ceramics, glass, refractories, electrical insulators and resistors, fluxes, dental cements, and chromatographic applications. | | Uses | 1'-Acetonaphthone is used in the preparation of S(-)-1-(1'-naphthyl) ethanol, an important synthetic intermediate of mevinic acid analog. | | General Description | Stereoselective reduction of 1-acetonapthone in aqueous media by whole cells of Geotrichum candidum has been investigated in various organic co-solvents. Magnetic field effects on the photoinduced electron-transfer reaction between 1-acetonaphthone and diphenylamine in micellar solution have been studied by laser flash photolysis. | | Flammability and Explosibility | Not classified | | Safety Profile | Moderately toxic by ingestion. A skin irritant. A combustible liquid. When heated to decomposition it emits acrid smoke and irritating fumes | | Synthesis | 1'-Acetonaphthone is produced from Naphthalene with Acetylchloride and Aluminum chloride (Friedel-Craft's synthesis) using Carbon disulfide as a solvent in order to favour the formation of alpha-isomer. | | Purification Methods | If the NMR spectrum indicates the presence of impurities, probably 2-acetylnaphthalene, convert the substance to its picrate by dissolving in *benzene or EtOH and adding excess of saturated picric acid in these solvents until separation of picrates is complete. Recrystallise the picrate till the melting point is 118o. Decompose the picrate with dilute NaOH and extract with Et2O. Dry the extract (Na2SO4), filter, evaporate and distil the residue. The 2,4-dinitrophenylhydrazone crystallises from EtOH and has m 259o. [Stobbe & Lenzer Justus Liebigs Ann Chem 380 95 1911, Williams & Osborne J Am Chem Soc 61 3438 1939, Beilstein 7 IV 1292.] |
| | 1'-Acetonaphthone Preparation Products And Raw materials |
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