204259-68-7 Usage
Description
1-Bromododecane-12,12,12-D3 is a deuterated organic compound with the chemical formula C12D3Br. It is isotopically labeled, which makes it a valuable research compound for various scientific studies and applications.
Uses
1. Used in Research Applications:
1-Bromododecane-12,12,12-D3 is used as a research compound for [application reason] in the field of [application industry]. The deuterium labeling in the molecule allows for enhanced detection and tracking in various experimental setups, making it a useful tool for studying chemical reactions, molecular interactions, and other scientific inquiries.
2. Used in Chemical Synthesis:
In the chemical synthesis industry, 1-Bromododecane-12,12,12-D3 is used as a starting material or intermediate for the production of other deuterated compounds. The presence of deuterium atoms can provide unique properties and advantages in the synthesis of specific chemicals, making it a valuable component in the development of novel materials and pharmaceuticals.
3. Used in Analytical Chemistry:
1-Bromododecane-12,12,12-D3 is employed as an internal standard or reference compound in analytical chemistry. Its deuterated nature allows for accurate quantification and identification of other compounds in complex mixtures, making it a crucial tool in various analytical techniques such as mass spectrometry and nuclear magnetic resonance (NMR) spectroscopy.
4. Used in Pharmaceutical Research:
In the pharmaceutical industry, 1-Bromododecane-12,12,12-D3 is utilized as a probe or marker in drug discovery and development. Its unique properties can help researchers understand the behavior of potential drug candidates, their interactions with biological targets, and their metabolic pathways, ultimately contributing to the design of more effective and safer medications.
5. Used in Material Science:
1-Bromododecane-12,12,12-D3 is also used in material science research to study the properties of deuterated materials. The incorporation of deuterium atoms can lead to altered physical and chemical characteristics, which can be beneficial in the development of advanced materials with specific applications, such as in electronics, energy storage, or sensors.
Check Digit Verification of cas no
The CAS Registry Mumber 204259-68-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,4,2,5 and 9 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 204259-68:
(8*2)+(7*0)+(6*4)+(5*2)+(4*5)+(3*9)+(2*6)+(1*8)=117
117 % 10 = 7
So 204259-68-7 is a valid CAS Registry Number.
204259-68-7Relevant articles and documents
2H NMR Evidence for dynamic disorder in human skin induced by the penetration enhancer Azone
Bezema,Marttin,Roemele,Brussee,Bodde,De Groot
, p. 785 - 791 (2007/10/03)
Penetration enhancers mediate trans-dermal drug delivery. The penetration enhancer dodecyl-azacycloheptanone (Azone) was characterized in situ with 2H NMR on human stratum corneum treated with either uniformly deuterated Azone or penetration enhancer with only the entire chain deuterated, in both cases in propylene glycol. The 2H NMR spectrum at ambient temperature constitutes a single narrow line only 180 Hz wide. This contrasts with the complex lineshapes 1-25 kHz wide commonly observed for methylene deuterons of lipids in a bilayer gel phase. Hence there is no evidence for differences in orientational behaviour between different deuterons at ambient temperature. The narrow line translates into a low overall order parameter SCD c 6 × 10-6 s, in all possible directions. At temperatures of about 150 K a 2H NMR pattern characteristic for a random isotropic powder was observed on samples of stacked stratum corneum sheets at different orientations with respect to the magnetic field. This provides strong evidence for random isotropic freezing of the Azone molecules upon cooling. The 2H NMR data suggest than incubation with Azone in propylene glycol provokes dynamic structural disorder of the intercellular lamellar lipid structure throughout the stratum corneum and possibly even the creation of fluid domains involving the intercellular lipids, which may be essential for the penetration enhancing effect.
