64118-16-7 Usage
Highly flammable
1-Butanol-3,3,4,4,4-D5 is a substance that can easily catch fire and cause a fire or explosion.
Toxic if ingested, inhaled, or absorbed through the skin
This chemical compound can cause harm to the human body if it is swallowed, breathed in, or comes into contact with the skin.
Causes skin and eye irritation
Contact with 1-Butanol-3,3,4,4,4-D5 can cause redness, itching, and irritation of the skin and eyes.
Used as a solvent
1-Butanol-3,3,4,4,4-D5 is commonly used as a solvent in various industrial and laboratory processes, including the extraction and purification of organic compounds.
Used in the production of plastics, coatings, and adhesives
This chemical compound is also used in the manufacturing of various products, including plastics, coatings, and adhesives.
Used in pharmaceutical manufacturing
1-Butanol-3,3,4,4,4-D5 is also used in the production of pharmaceuticals.
Caution required
Due to its toxic and flammable nature, it is important to exercise caution when handling and using 1-Butanol-3,3,4,4,4-D5 in any setting.
Check Digit Verification of cas no
The CAS Registry Mumber 64118-16-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,1,1 and 8 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 64118-16:
(7*6)+(6*4)+(5*1)+(4*1)+(3*8)+(2*1)+(1*6)=107
107 % 10 = 7
So 64118-16-7 is a valid CAS Registry Number.
64118-16-7Relevant articles and documents
Biosynthesis of epilachnene, a macrocyclic defensive alkaloid of the Mexican bean beetle
Attygalle, Athula B.,Svatos, Ales,Veith, Martin,Farmer, Jay J.,Meinwald, Jerrold,Smedley, Scott,Gonzalez, Andres,Eisner, Thomas
, p. 955 - 966 (2007/10/03)
The carbon skeleton of the azamacrolide epilachnene, the principal defensive alkaloid of Epilachna varivestis pupae, can be derived from oleic acid and serine. Analytical evidence from three experiments in which insects were fed (2H35)octadecanoic acid, (Z)-9- [11,11,12,12,13,13,14,14,15,15,16,16,17,17,18,18,18-2H17]octadecenoic acid and (Z)-9-[11,11,12,12,13,13,14,14,16,16,17,17,18,18,18-2H15]octadecenoic acid, indicates that only the C-15 methylene group of oleic acid is involved in the mechanism leading to carbon-nitrogen bond formation in epilachnene. Support for this scheme is provided by the observation of an unusual ion at m/z 170 in the electron-ionization mass spectrum of epilachnene, rationalized as CH2=CH-COO-CH2-CH2-NH+=CH-CH2-CH2-CH3.
