91732-68-2

Basic information

• Product Name: 1-BUTANOL-2,2,3,3,4,4,4-D7
• Synonyms: N-BUTYL-2,2,3,3,4,4,4-D7 ALCOHOL;N-BUTANOL (2,2,3,3,4,4,4-D7);1-BUTANOL-2,2,3,3,4,4,4-D7;BUTYL ALCOHOL (2,2,3,3,4,4,4-D7);n-Butyl--d7 Alcohol
• CAS NO: 91732-68-2
• Molecular Formula: C4H3D7O
• Molecular Weight: 81.16
• Mol File: 91732-68-2.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1-BUTANOL-2,2,3,3,4,4,4-D7(CAS DataBase Reference)
• NIST Chemistry Reference: 1-BUTANOL-2,2,3,3,4,4,4-D7(91732-68-2)
• EPA Substance Registry System: 1-BUTANOL-2,2,3,3,4,4,4-D7(91732-68-2)

Safety Data

• Hazardous Substances Data: 91732-68-2(Hazardous Substances Data)

Usage

Molecular weight

Higher than regular 1-butanol (The presence of seven deuterium atoms increases the molecular weight of the compound)

Stability

Stable isotope-labeled form (The deuterium atoms make the compound more stable and less reactive)

Usage

Used as a labeled standard or internal standard in gas chromatography-mass spectrometry (GC-MS) and other analytical methods (The deuterated form helps in accurately measuring and identifying the presence and quantity of 1-butanol in various samples)

Application

Valuable tool in research and industrial applications (It helps in the analysis of complex mixtures and the identification of specific chemicals)

Deuterium atoms

Seven (The compound contains seven deuterium atoms, making it heavier than regular 1-butanol)

Upstream product

• 156779-02-1 4,4,4,3,3,2,2-d₇-butanoic acid 

Downstream Products

• 223487-53-4 1-bromo-<2,2,3,3,4,4,4-(2)H7>butane 
• 951209-46-4 2,2,3,3,4,4,4-d7-butyraldehyde 

Relevant articles and documents

Biosynthesis of epilachnene, a macrocyclic defensive alkaloid of the Mexican bean beetle

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.