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| 2,3-DIMETHYLACRYLONITRILE | ||
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PRODUCT IDENTIFICATION |
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| CAS NO. | 4403-61-6
(racemic) 20068-02-4 (cis) 30574-97-1 (trans) |
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| EINECS NO. | 224-544-5, 243-496-6, 250-247-5 | |
| FORMULA | CH3CH=C(CH3)CN | |
| MOL WT. | 81.12 | |
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H.S. CODE |
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TOXICITY |
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| SYNONYMS | 2-Metil-2-butenonitrilo; 2-Méthyl-2-butènenitrile; | |
| 2-Methyl-2-butenenitrile; 2-Methylcrotononitrile; alpha,beta-Dimethylacrylonitrile; alpha-Methylcrotononitrile; | ||
| DERIVATION | ||
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CLASSIFICATION |
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PHYSICAL AND CHEMICAL PROPERTIES |
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| PHYSICAL STATE | clear liquid | |
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MELTING POINT |
- 12 C | |
| BOILING POINT |
122 C | |
| SPECIFIC GRAVITY | ||
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SOLUBILITY IN WATER |
<0.1 g/100ml | |
| pH | ||
| VAPOR DENSITY | ||
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AUTOIGNITION |
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NFPA RATINGS |
Health (H) : 3 Flammability (F) : 3 Reactivity (R) : 1 | |
| REFRACTIVE INDEX |
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FLASH POINT |
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| STABILITY | ||
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GENERAL DESCRIPTION & 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, cyclizized to pyridine derivatives. 2,3-Dimethylacrylonitrile finds applications in dye and flavour & fragrance manufacturing, rubber chemicals, and lubricant as well as a monomer. |
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| SALES SPECIFICATION | ||
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APPEARANCE |
clear liquid | |
| CONTENT |
95.0% min (2-Methyl-2-butenenitrile + 2-Methyl-3-butenenitrile) | |
| BUTADIENE |
5.0% max | |
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HCN |
30ppm max | |
| TRANSPORTATION | ||
| PACKING | 160kgs in drum | |
| HAZARD CLASS | 3, 6.1 (Packing Group: II) | |
| UN NO. | 3273 | |
| OTHER INFORMATION | ||
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Hazard Symbols: F XN, Risk Phrases: 11-20/22, Safety Phrases: 16-23 |
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