- 2-Cyclohexylethanol
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- $0.00 / 25KG
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2024-03-28
- CAS:4442-79-9
- Min. Order: 25KG
- Purity: ≥95%
- Supply Ability: Inquiry
- 2-Cyclohexylethanol
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- $0.00 / 1kg
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2023-09-12
- CAS:4442-79-9
- Min. Order: 1kg
- Purity: 0.99
- Supply Ability: 20tons
- 2-Cyclohexylethanol
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- $10.00 / 1KG
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2023-04-07
- CAS:4442-79-9
- Min. Order: 1KG
- Purity: 99%
- Supply Ability: 10 mt
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| 2-Cyclohexylethanol Basic information |
Product Name: | 2-Cyclohexylethanol | Synonyms: | 2-Cyclohexyl-1-ethanol;2-Cyclohexylethanol,(2-Hydroxyethyl)cyclohexane;2-CYCLOHEXYLETHANOL FOR SYNTHESIS;(2-HYDROXYETHYL)CYCLOHEXANE;2-CYCLOHEXYLETHANOL;2-CYCLOHEXANEETHANOL;CYCLOHEXANEETHANOL;CYCLOHEXANETHANOL | CAS: | 4442-79-9 | MF: | C8H16O | MW: | 128.21 | EINECS: | 224-672-1 | Product Categories: | Alkohols;Industrial/Fine Chemicals | Mol File: | 4442-79-9.mol | |
| 2-Cyclohexylethanol Chemical Properties |
Melting point | -20 °C | Boiling point | 206-207 °C/745 mmHg (lit.) | density | 0.919 g/mL at 25 °C (lit.) | vapor pressure | 0.2 hPa (25 °C) | refractive index | n20/D 1.465(lit.) | Fp | 188 °F | storage temp. | Store below +30°C. | pka | 15.19±0.10(Predicted) | form | clear liquid | color | A colourless oily liquid. | Odor | at 100.00 %. floral waxy cool green peony lily dewy rose | Odor Type | floral | explosive limit | 0.9-6.3%(V) | Water Solubility | insoluble | BRN | 1848152 | LogP | 2.301 (est) | CAS DataBase Reference | 4442-79-9(CAS DataBase Reference) | NIST Chemistry Reference | Cyclohexaneethanol(4442-79-9) | EPA Substance Registry System | Cyclohexaneethanol (4442-79-9) |
Hazard Codes | Xn | Risk Statements | 21/22 | Safety Statements | 26-28-36/37/39 | WGK Germany | 3 | RTECS | KK3528000 | TSCA | Yes | HS Code | 29061900 | Toxicity | LD50 orally in Rabbit: 940 mg/kg LD50 dermal Rabbit 1220 mg/kg |
| 2-Cyclohexylethanol Usage And Synthesis |
Chemical Properties | clear colourless liquid | Occurrence | Has apparently not been reported to occur in nature | Uses | 2-Cyclohexylethanol is a useful building block, and has recently been used in a green preparation of oxidative esterification of primary alcohols. | Preparation | By catalytic hydrogenation of phenylethyl alcohol under pressure (Arctander, 1969). | Synthesis Reference(s) | Journal of the American Chemical Society, 108, p. 1325, 1986 DOI: 10.1021/ja00266a049 |
| 2-Cyclohexylethanol Preparation Products And Raw materials |
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