1-Butanethiol, 3,3-dimethyl- is an organic compound classified as a thiol, characterized by the presence of a sulfhydryl (-SH) group. Its molecular structure features a butane backbone with two additional methyl groups attached to the third carbon, resulting in a branched structure. This compound is typically a colorless liquid with a strong, unpleasant odor reminiscent of garlic or rotten cabbage, which is common among thiols. It is soluble in organic solvents and exhibits low solubility in water due to its hydrophobic hydrocarbon chain. 1-Butanethiol, 3,3-dimethyl- is used in various applications, including as a flavoring agent and in the synthesis of other chemical compounds. It is important to handle this substance with care, as thiols can be toxic and irritating to the skin and respiratory system. Additionally, it may undergo reactions typical of thiols, such as oxidation to form disulfides or reactions with electrophiles. Overall, this compound is notable for its distinctive odor and reactivity, making it significant in both industrial and laboratory settings.

1-Butanethiol, 3,3-dimethyl-

1638-98-8: 1-Butanethiol, 3,3-dimethyl- is an organic compound classified as a thiol, characterized by the presence of a sulfhydryl (-SH) group. Its molecular structure features a butane backbone with two additional methyl groups attached to the third carbon, resulting in a branched structure. This compound is typically a colorless liquid with a strong, unpleasant odor reminiscent of garlic or rotten cabbage, which is common among thiols. It is soluble in organic solvents and exhibits low solubility in water due to its hydrophobic hydrocarbon chain. 1-Butanethiol, 3,3-dimethyl- is used in various applications, including as a flavoring agent and in the synthesis of other chemical compounds. It is important to handle this substance with care, as thiols can be toxic and irritating to the skin and respiratory system. Additionally, it may undergo reactions typical of thiols, such as oxidation to form disulfides or reactions with electrophiles. Overall, this compound is notable for its distinctive odor and reactivity, making it significant in both industrial and laboratory settings.

CAS 1638-98-8

1-Butanethiol, 3,3-dimethyl-