453-17-8
453-17-8
Chemical Structure
(R)-2,3-Dihydroxypropanal, 80%
- CAS No.: 453-17-8
- Formula:C3H6O3
- Molecular Weight:90.08
IUPAC Name: (R)-2,3-dihydroxypropanal
InChIKey: MNQZXJOMYWMBOU-VKHMYHEASA-N
SMILES: OC[C@@H](O)C=O
Biological Activity: (R)-2,3-Dihydroxypropanal, 80% is a biochemical assay reagent.
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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(R)-2,3-Dihydroxypropanal, 80% | 99.1% | (R)-2,3-Dihydroxypropanal, 80% is a biochemical assay reagent. | ||||||||||||||||||||
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(R)-2,3-Dihydroxypropanal-d | (R)-2,3-Dihydroxypropanal-d is the deuterium labeled (R)-2,3-Dihydroxypropanal. | |||||||||||||||||||||
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(R)-2,3-Dihydroxypropanal-d2 | (R)-2,3-Dihydroxypropanal-d2 is the deuterium labeled 3-O-Methyl-D-glucopyranose. | |||||||||||||||||||||
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(R)-2,3-Dihydroxypropanal-3-13C | (R)-2,3-Dihydroxypropanal-3-13C is the 13C labeled (R)-2,3-Dihydroxypropanal. | |||||||||||||||||||||
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(R)-2,3-Dihydroxypropanal-d4 | (R)-2,3-Dihydroxypropanal-d4 is the deuterium labeled (R)-2,3-Dihydroxypropanal. | |||||||||||||||||||||
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D-Erythrose (50%w/w in water) | 95.41% | D-Erythrose is a four-carbon sugar classified as an aldose. D-Erythrose has unique chemical properties that make it an important intermediate in various metabolic pathways, especially in the biosynthesis of amino acids and nucleotides. It also plays a role in the pentose phosphate pathway, which generates reducing equivalents for biosynthetic reactions and cellular defense against oxidative damage. | ||||||||||||||||||||
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L-Erythrose (solution) (70%w/w in water) | L-Erythrose (solution) (70% in water) is an aldose carbohydrate that has been used in glycation studies and to characterize erythrose reductase activity. | |||||||||||||||||||||
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D-Erythrose-1-13C | D-Erythrose-1-13C is the 13C labeled D-Erythrose. | |||||||||||||||||||||
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DL-Glyceraldehyde | 90.0% | DL-Glyceraldehyde is a bioactive substance involved in cellular energy metabolism and a key intermediate in sugar metabolism pathways (such as glycolysis and gluconeogenesis). During glycolysis, DL-Glyceraldehyde is converted by enzymes into other metabolites to provide energy for cells; during gluconeogenesis, DL-Glyceraldehyde participates in the synthesis of glucose as a precursor. In the field of medical research, DL-Glyceraldehyde can be used to study diseases related to sugar metabolism, such as diabetes, tumors, etc |
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DL-Glyceraldehyde-1-13C | DL-Glyceraldehyde-1-13C is the 13C labeled DL-Glyceraldehyde. | |||||||||||||||||||||
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DL-Glyceraldehyde-2-13C | DL-Glyceraldehyde-2-13C is the 13C labeled DL-Glyceraldehyde. | |||||||||||||||||||||
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DL-Glyceraldehyde-13C3 | DL-Glyceraldehyde-13C3 is the 13C labled DL-Glyceraldehyde (HY-128748). DL-Glyceraldehyde is an organic compound. | |||||||||||||||||||||
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L-(−)-Glyceraldehyde | 94% | L-(-)-Glyceraldehyde serves as a crucial intermediate in the metabolic pathways of carbohydrates. | ||||||||||||||||||||
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(2S,3R)-2,3,4-Trihydroxybutanal-13C-1 | 99.9% | (2S,3R)-2,3,4-Trihydroxybutanal-13C-1 is the 13C labeled (2S,3R)-2,3,4-Trihydroxybutanal. | ||||||||||||||||||||
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