13330-96-6 Usage
General Description
4-DIMETHYLAMINO-1-BUTANOL, also known as N,N-dimethyl-2-amino-1-butanol, is a synthetic chemical compound commonly used as a solvent and in the production of pharmaceuticals, dyes, and rubber chemicals. It is a clear, colorless liquid with a faint amine odor and is highly soluble in water. This chemical is often used as a corrosion inhibitor and as an intermediate in the synthesis of other organic compounds. It has been found to have low acute toxicity, but prolonged exposure through inhalation or skin contact can cause irritation to the respiratory system and skin. Additionally, it has been shown to be potentially harmful if ingested or absorbed through the skin in large quantities. Proper handling and safety precautions should be taken when working with 4-DIMETHYLAMINO-1-BUTANOL.
Check Digit Verification of cas no
The CAS Registry Mumber 13330-96-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,3,3 and 0 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 13330-96:
(7*1)+(6*3)+(5*3)+(4*3)+(3*0)+(2*9)+(1*6)=76
76 % 10 = 6
So 13330-96-6 is a valid CAS Registry Number.
InChI:InChI=1/C6H15NO/c1-7(2)5-3-4-6-8/h8H,3-6H2,1-2H3
13330-96-6Relevant articles and documents
Synthesis and pharmacological effects of bis-trialkylammonium alkanol carbonates.
POHORYLES,WISLICKI,SAREL
, p. 348 - 351 (1962)
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Budzikiewicz,Pesch
, p. 861,875 (1974)
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Enhanced product selectivity in continuous N-methylation of amino alcohols over solid acid-base catalysts with supercritical methanol
Oku, Tomoharu,Ikariya, Takao
, p. 3476 - 3479 (2007/10/03)
The unique properties of supercritical fluids can be exploited for fine-tuning product selectivity. Under the conditions listed for the N-methylation of amino alcohols (see scheme) over solid acid-base bifunctional catalysts, the total yield and product selectivity could be improved. Enhanced product selectivity might be attributed to the milder reaction conditions possible with supercritical methanol, as well as the increased concentration of methanol on the catalyst.
Addition-Rearrangement Reactions of N-(Arylsulphonyloxy)amines and 3,4-Dihydro-2H-pyran
Hoffman, Robert V.,Salvador, James M.
, p. 1375 - 1380 (2007/10/02)
A series of N-alkyl-O-(arylsulphonyl)hydroxylamines (NSA) was treated with 3,4-dihydro-2H-pyran (DHP).Acid-catalysed addition to the double bond followed by cationic rearrangement gave cyclic imidates from hydride migration (major) and ring expansion (min
