06372
β-Hydroxypyruvic acid
≥95.0% (dry substance, T)
Synonyme(s) :
3-Hydroxy-2-oxopropanoic acid
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| Conditionnement | Référence | Disponibilité | Prix |
|---|---|---|---|
| 5 mg | Veuillez contacter notre Service Clients pour connaître la disponibilité de ce produit. | 208,00 $ | |
| 25 mg | Veuillez contacter notre Service Clients pour connaître la disponibilité de ce produit. | 821,00 $ |
A propos de cet article
Formule empirique (notation de Hill) :
C3H4O4
Numéro CAS:
Poids moléculaire :
104.06
UNSPSC Code:
12352204
PubChem Substance ID:
NACRES:
NA.32
MDL number:
Assay:
≥95.0% (dry substance, T)
Form:
powder and chunks
208,00 $
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assay
≥95.0% (dry substance, T)
form
powder and chunks
impurities
≤15.0% water
storage temp.
2-8°C
InChI
1S/C3H4O4/c4-1-2(5)3(6)7/h4H,1H2,(H,6,7)
InChI key
HHDDCCUIIUWNGJ-UHFFFAOYSA-N
Application
- Hydroxy(phenyl)pyruvic acid reductase in Actaea racemosa L.: a putative enzyme in cimicifugic and fukinolic acid biosynthesis.: This study investigates the role of β-Hydroxypyruvic acid in the biosynthesis of bioactive compounds in Actaea racemosa, highlighting its importance in plant secondary metabolism and potential applications in medicinal chemistry (Jahn and Petersen, 2024).
- The gut microbiota confers protection in the CNS against neurodegeneration induced by manganism.: Research shows the protective role of β-Hydroxypyruvic acid derivatives produced by gut microbiota against neurodegenerative conditions, providing insights into therapeutic strategies for neurological disorders (Wang et al., 2020).
Biochem/physiol Actions
Metabolite involved in the pathway of carbon in photorespiration[1].
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Cet article | |||
|---|---|---|---|
| assay ≥95.0% (dry substance, T) | assay 95% | assay ≥97% | assay 98% |
| Quality Level 100 | Quality Level 200 | Quality Level 100 | Quality Level 200 |
| form powder and chunks | form - | form - | form - |
| storage temp. 2-8°C | storage temp. 2-8°C | storage temp. −20°C | storage temp. 2-8°C |
| impurities ≤15.0% water | impurities - | impurities - | impurities - |
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Skin Corr. 1B
Classe de stockage
8A - Combustible corrosive hazardous materials
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
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Seong Pil Chung et al.
Journal of biochemistry, 148(6), 743-753 (2010-09-30)
D-amino acid oxidase (DAO) is a flavoenzyme that exists in the kidney, liver and brain of mammals. This enzyme catalyzes the oxidation of D-amino acids to the corresponding α-keto acid, hydrogen peroxide and ammonia. Recently D-serine, one of the substrates
Chen Yang et al.
Journal of bacteriology, 190(5), 1773-1782 (2007-12-25)
Members of a novel glycerate-2-kinase (GK-II) family were tentatively identified in a broad range of species, including eukaryotes and archaea and many bacteria that lack a canonical enzyme of the GarK (GK-I) family. The recently reported three-dimensional structure of GK-II
Juhan Kim et al.
Proceedings of the National Academy of Sciences of the United States of America, 109(42), E2856-E2864 (2012-09-18)
Evolution or engineering of novel metabolic pathways can endow microbes with new abilities to degrade anthropogenic pollutants or synthesize valuable chemicals. Most studies of the evolution of new pathways have focused on the origins and quality of function of the
Numéro d'article de commerce international
| Référence | GTIN |
|---|---|
| C94807-100G | 04061833530733 |
| PHR2087-100MG | 04061835234646 |
| C94807-5G | 04061833530740 |
| 06372-25MG-F | 04061838646040 |
| 06372-5MG-F | 04061838646132 |