615080
2-Propanol-OD
98 atom % D
Synonym(s):
2-Propan(ol-d), Isopropanol-OD, Isopropyl alcoh(ol-d)
Sign Into View Organizational & Contract Pricing
All Photos(1)
About This Item
Recommended Products
isotopic purity
98 atom % D
Quality Level
Assay
99% (CP)
refractive index
n20/D 1.3752 (lit.)
bp
82 °C (lit.)
mp
-90 °C (lit.)
density
0.798 g/mL at 25 °C (lit.)
mass shift
M+1
SMILES string
[2H]OC(C)C
InChI
1S/C3H8O/c1-3(2)4/h3-4H,1-2H3/i4D
InChI key
KFZMGEQAYNKOFK-QYKNYGDISA-N
Looking for similar products? Visit Product Comparison Guide
General description
2-Propanol-OD, isotopically labeled analogue of 2-propanol.
Application
2-Propanol- OD is used as a solvent to study the reaction mechanism of benzophenone and/or acetone ketyl radicals with tirapazamine, which is used to examined the exact mechanism of DNA damage and repair. Also, it is used to monitor the solvation of carbene compounds from dynamic study.
2-Propanol-OD can be used as a solvent in the study of:
- Solvation time (dynamics) of singlet carbene compounds.
- Reaction mechanism of benzophenone and/or acetone ketyl radicals with tirapazamine.
Packaging
This product may be available from bulk stock and can be packaged on demand. For information on pricing, availability and packaging, please contact Stable Isotopes Customer Service.
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Flam. Liq. 2 - STOT SE 3
Target Organs
Central nervous system
Storage Class Code
3 - Flammable liquids
WGK
WGK 1
Flash Point(F)
53.6 °F - closed cup
Flash Point(C)
12.0 °C - closed cup
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Customers Also Viewed
Journal of the American Chemical Society, 129(15), 4542-4550 (2007-03-27)
Ketyl radicals produced by photolysis of ketones or di-tert-butyl peroxide (DTBP) in alcohol solvents react rapidly with tirapazamine (TPZ). The acetone ketyl radical (ACOH) reacts with TPZ with an absolute second-order rate constant of (9.7 +/- 0.4) x 108 M-1
The dynamics of carbene solvation: an ultrafast study of p-biphenylyltrifluoromethylcarbene
Journal of the American Chemical Society, 130(7), 2304-2313 (2008)
On the mechanism of reaction of radicals with tirapazamine
Journal of the American Chemical Society, 129(15), 4542-4550 (2007)
Journal of the American Chemical Society, 130(7), 2304-2313 (2008-01-25)
Ultrafast photolysis (lambda(ex) = 308 nm) of p-biphenylyltrifluoromethyl diazomethane (BpCN2CF3) releases singlet p-biphenylyltrifluoromethylcarbene (BpCCF3) which absorbs strongly at 385 nm in cyclohexane, immediately after the 300 fs laser pulse. The initial absorption maximum shifts to longer wavelengths in coordinating solvents
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service