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isotopic purity
98 atom % D
form
solid
optical activity
[α]25/D +79.0, c = 2 in H2O (trace NH4OH)
mp
169-170 °C (lit.)
suitability
endotoxin tested
mass shift
M+1
SMILES string
[2H][C@]1(O)O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O
InChI
1S/C6H12O6/c7-1-2-3(8)4(9)5(10)6(11)12-2/h2-11H,1H2/t2-,3+,4+,5-,6?/m1/s1/i6D
InChI key
WQZGKKKJIJFFOK-RUIMULFXSA-N
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Related Categories
1 of 4
This Item | 661406 | 495077 | 454621 |
|---|---|---|---|
| isotopic purity 98 atom % D | isotopic purity 99 atom % 13C | isotopic purity 98 atom % D | isotopic purity 99 atom % 13C |
| mass shift M+1 | mass shift M+1 | mass shift M+1 | mass shift M+1 |
| form solid | form solid | form solid | form solid |
| mp 169-170 °C (lit.) | mp 169-170 °C (lit.) | mp 169-170 °C (lit.) | mp 170-172 °C (lit.) |
| optical activity [α]25/D +79.0, c = 2 in H2O (trace NH4OH) | optical activity [α]25/D +79.0, c = 2 in H2O (trace NH4OH) | optical activity [α]25/D +79.0, c = 2 in H2O (trace NH4OH) | optical activity [α]25/D +79.0, c = 2 in H2O (trace NH4OH) |
| suitability endotoxin tested | suitability endotoxin tested | suitability - | suitability - |
General description
Application
- Chemical synthesis of labeled compounds
- Analytical method development
- Pharmaceutical formulation development
Features and Benefits
- Ideal for use in Advanced imaging protocols.
- Supports high-resolution imaging techniques.
- Enhances the effectiveness of diagnostic procedures.
- Facilitates collaboration in clinical research.
Benefits
- Drives innovation in imaging techniques.
- Increases patient engagement and satisfaction.
- Facilitates collaboration with research institutions.
- Improves patient outcomes through Advanced diagnostics.
Packaging
Storage Class
11 - Combustible Solids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
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