CAS 1609-86-5

Propane, 2-isocyanato-2-methyl-

Description:

Propane, 2-isocyanato-2-methyl-, also known as isocyanato-2-methylpropane, is an organic compound characterized by the presence of an isocyanate functional group (-N=C=O) attached to a branched propane structure. This compound is typically a colorless to pale yellow liquid with a pungent odor, indicative of the isocyanate group. It is known for its reactivity, particularly in forming urethane linkages when it reacts with alcohols or amines, making it valuable in the production of polyurethanes and other polymers. The compound is also recognized for its potential health hazards; it can be a respiratory irritant and is classified as a skin sensitizer. Proper handling and safety precautions are essential when working with this substance, as exposure can lead to adverse health effects. Additionally, it is important to note that isocyanates can undergo hydrolysis in the presence of moisture, leading to the formation of corresponding amines and carbon dioxide.

Formula: C₅H₉NO

InChI: InChI=1S/C5H9NO/c1-5(2,3)6-4-7/h1-3H3

InChI key: InChIKey=MGOLNIXAPIAKFM-UHFFFAOYSA-N

SMILES: N(C(C)(C)C)=C=O

Synonyms:

• 1,1-Dimethylethyl isocyanate
• 2-Isocyanato-2-methylpropane
• Isocianato De Terc-Butilo
• Isocyanate de tert-butyle
• Isocyanic acid, tert-butyl ester
• Tert-Butyl Isocyanate
• t-Butylisocyanate
• tert-Butylisocyanat
• 2-Methyl-2-isocyanopropane
• Butylisocyanate
• 1,1-dimethylethylisocyanate
• 2-isocyanato-2-methyl-propan
• left-Butyl isocyanate
• T-BUTYLISOCYANIDE
• 2-ISOCYANO-2-METHYL-PROPANE
• Propane, 2-isocyano-2-methyl-
• 2-isocyano-2-methyl-propan
• Propane, 2-isocyanato-2-methyl-
• tert-Butylisocyanate

tert-Butyl Isocyanate

CAS: 1609-86-5

Formula: C₅H₉NO

Molecular weight: 99.13

Ref: 4Z-I-131005

tert-Butylisocyanate

CAS: 1609-86-5

Tert-butylisocyanate is a reactive chemical that contains a carboxylate group. It is an ester hydrochloride that can be synthesized by reacting trifluoroacetic acid with molybdenum trioxide. This compound has been studied using X-ray crystal structures and the intramolecular hydrogen transfer reaction between two nitrogen atoms in the molecule. Tert-butylisocyanate is stable in solution because it does not react with water or alkalis, but does react with sodium carbonate, forming sodium cyanate and tetrabutylammonium hydroxide. Tert-butylisocyanate reacts with inorganic acids such as sulfuric acid to form its corresponding salts. The chelate ligand of tert-butylisocyanate prevents it from reacting with transition metals such as copper and iron, but will react with zinc metal.

Formula: C₅H₉NO

Purity: Min. 98 Area-%

Color and Shape: Colorless Clear Liquid

Molecular weight: 99.13 g/mol

Ref: 3D-FB01362

tert-Butylisocyanate

CAS: 1609-86-5

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Formula: C₅H₉NO

Purity: Min. 98.5 Area-%

Molecular weight: 99.13 g/mol

Ref: 3D-W-107973

t-Butyl Isocyanate

CAS: 1609-86-5

Formula: C₅H₉NO

Color and Shape: Colourless Oil

Molecular weight: 99.13

Ref: TR-B693325