- 3-Methoxypropionitrile
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- $0.00 / 25kg
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2025-12-01
- CAS:110-67-8
- Min. Order: 1kg
- Purity: 99%
- Supply Ability: 10000KGS
- 3-Methoxypropionitrile
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- $1.00 / 1KG
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2019-07-06
- CAS:110-67-8
- Min. Order: 1KG
- Purity: 95%-99.99%
- Supply Ability: 1kg-10MT
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| | 3-Methoxypropionitrile Basic information |
| | 3-Methoxypropionitrile Chemical Properties |
| Melting point | -62.9 °C | | Boiling point | 164-165 °C (lit.) | | density | 0.937 g/mL at 25 °C (lit.) | | vapor pressure | 2.3 hPa (30 °C) | | refractive index | n20/D 1.403(lit.) | | Fp | 66 °C | | storage temp. | 2-8°C | | solubility | 540g/l | | form | Liquid | | Specific Gravity | 0.946 | | color | Clear colorless to yellow | | PH | 6.8 (111g/l, H2O, 25℃) | | explosive limit | 1.9-15.3%(V) | | Water Solubility | 335 g/L (20 ºC) | | BRN | 1739284 | | InChI | 1S/C4H7NO/c1-6-4-2-3-5/h2,4H2,1H3 | | InChIKey | OOWFYDWAMOKVSF-UHFFFAOYSA-N | | SMILES | COCCC#N | | CAS DataBase Reference | 110-67-8(CAS DataBase Reference) | | NIST Chemistry Reference | 3-Methoxypropionitrile(110-67-8) | | EPA Substance Registry System | Propanenitrile, 3-methoxy- (110-67-8) |
| Hazard Codes | Xi | | Risk Statements | 36/37/38 | | Safety Statements | 26-36-37/39 | | RIDADR | 3276 | | WGK Germany | 2 | | RTECS | TZ4870000 | | Autoignition Temperature | 390 °C DIN 51794 | | TSCA | TSCA listed | | HazardClass | 3.2 | | PackingGroup | III | | HS Code | 29269095 | | Storage Class | 10 - Combustible liquids | | Hazard Classifications | Eye Irrit. 2 | | Toxicity | LD50 orally in Rabbit: 4130 mg/kg LD50 dermal Rabbit > 9400 mg/kg |
| | 3-Methoxypropionitrile Usage And Synthesis |
| Chemical Properties | clear colorless to yellow liquid | | Uses | 3-Methoxypropionitrile is used as a component in high power lithium ion batteries. It is used as pharmaceutical intermediates. It acts as a good solvent for plastic polymers. | | Synthesis | GENERAL PROCEDURE: To a solution of activated 2-acrylonitrile (0.5 mmol) in methanol (2.0 mmol) was added Na2CO3 (0.2 mL, 0.05 M aqueous solution) and the reaction mixture was stirred until the 2-acrylonitrile was either completely consumed (monitored by TLC) or a predetermined reaction time was reached. Upon completion of the reaction, the reaction mixture was extracted with ethyl acetate (3 x 5 mL). The organic layers were combined, washed with brine (10 mL), dried over anhydrous Na2SO4, filtered, and concentrated under reduced pressure. The crude product was purified by silica gel column chromatography to give 3-methoxypropionitrile. | | References | [1] Inorganic Chemistry, 2010, vol. 49, # 13, p. 6203 - 6213
[2] Tetrahedron, 2011, vol. 67, # 14, p. 2562 - 2569
[3] Tetrahedron, 1981, vol. 37, # 16, p. 2905 - 2908
[4] Tetrahedron Letters, 2014, vol. 55, # 49, p. 6718 - 6720
[5] Journal of the American Chemical Society, 2003, vol. 125, # 29, p. 8696 - 8697 |
| | 3-Methoxypropionitrile Preparation Products And Raw materials |
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