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2-METHYL-3-BUTENENITRILE | ||
PRODUCT IDENTIFICATION |
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CAS NO. | 16529-56-9 |
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EINECS NO. | 240-596-1 | |
FORMULA | C5H7N | |
MOL WT. | 81.12 | |
H.S. CODE |
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TOXICITY |
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SYNONYMS | 2,3-Methylbutenenitrile 2M3BN 2-Methyl Allylcyanide | |
3-Cyanobutene-1 3-Butenenitrile, 2-Methyl- | ||
PRICE | ||
CLASSIFICATION |
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PHYSICAL AND CHEMICAL PROPERTIES |
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PHYSICAL STATE | Clear to yellow liquid | |
MELTING POINT | ||
BOILING POINT | 121 C | |
SPECIFIC GRAVITY |
0.81 | |
SOLUBILITY IN WATER | 1-5 g/100 ml but soluble in acetone, ethanol | |
pH | ||
VAPOR PRESSURE | 12 mmHg | |
REFRACTIVE INDEX |
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NFPA RATINGS |
Health (H) : 3 Flammability (F) : 3 Reactivity (R) : 1 | |
AUTOIGNITION |
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FLASH POINT |
15 C | |
STABILITY | ||
APPLICATIONS |
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Intermediates provide functional groups, building blocks, possibilities for motif modifications, and leaving group to create a desired chemical compound through a series of chemical reactions. 2-Methyl-2-Butenenitrile, 2,3-Dimethylacrylonitrile in acrylic system name, has a branch, carbon-carbon solid bond and nitrile functional group. Its unsaturated bond enables a series of addition reactions at beta carbon, producing methyl branched derivatives including tiglic acid and angelic acid and their derivatives. Tiglic acid is structurally the trans- form of methyl branched crotonic acid found in croton oil (trans-2,3-Dimethylacrylic acid in acrylic acid series naming). The cis- form of methyl branched crotonic acid is called angelic acid obtainable naturally from roots of Angelica plant. A large number of inorganic or organic reagents, can be added to this unsaturated bond.
Although nitriles don't have a carbonyl group, they are often considered as derivatives of carboxylic acids. Nitrile undergoes acid hydrolysis to form a carboxylic acid. Nitrile is reduced to form amine in the presence of nickel catalyst. Grignard reagents add to nitriles, forming a relatively stable imino derivative which can be hydrolyzed to a ketone. Metaloimine is hydrolyzed to give beta-ketoester. Nitrile undergoes a sequence of nucleophilic additions with an alcohol under acid catalysis, called nitrile alcoholysis. Nitriles are hydrolyzed to carboxylic acids, alcoholyzed to esters, reduction to amines, cyclized to pyridine derivatives. 2-Methyl-3-butenenitrile finds applications in dye and flavour & fragrance manufacturing, rubber chemicals, and lubricant as well as a monomer. |
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SALES SPECIFICATION | ||
APPEARANCE |
Clear to yellow liquid | |
CONTENT |
85.0% min | |
TRANS ISOMER |
4.0% max | |
PENTENENITRILES |
10.0% max | |
MOISTURE |
0.2% max | |
TRANSPORTATION | ||
PACKING | 160kgs in Drum | |
HAZARD CLASS | 3 | |
UN NO. |
1993 | |
OTHER INFORMATION | ||
Hazard Symbols: F XN, Risk Phrases: 11-20/22, Safety Phrases: 16-23 |
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