61932
DL-3,3-Dimethylmalic acid
≥97.0% (GC)
Synonym(s):
3-Hydroxy-2,2-dimethylbutanedioic acid, 3-Hydroxy-2,2-dimethylsuccinic acid
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About This Item
Empirical Formula (Hill Notation):
C6H10O5
CAS Number:
Molecular Weight:
162.14
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
1777593
assay
≥97.0% (GC)
mp
120-130 °C
application(s)
clinical testing
format
neat
storage temp.
2-8°C
SMILES string
OC(C(O)C(C)(C)C(O)=O)=O
InChI
1S/C6H10O5/c1-6(2,5(10)11)3(7)4(8)9/h3,7H,1-2H3,(H,8,9)(H,10,11)
InChI key
KSAIICDEQGEQBK-UHFFFAOYSA-N
Biochem/physiol Actions
Metabolite of the pantothenate and coenzyme A biosynthesis.
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
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Junliang Hao et al.
Current topics in medicinal chemistry, 14(15), 1789-1841 (2014-09-02)
Metabotropic glutamate receptor 5 (mGlu5) is a class C G-protein-coupled receptor which possesses a large extracellular N-terminal domain (ATD) connected to the seven-transmembrane (7-TM) domain. In contrast to the glutamate and its close analogs binding at the orthosteric site on
Farid Ouhib et al.
Macromolecular bioscience, 5(4), 299-305 (2005-04-09)
Amphiphilic and biodegradable micelles and nanoparticles designed as potential drug carriers were prepared from biodegradable statistical and block copolyesters obtained by a living anionic ring-opening process. These novel materials display amphiphilic properties arising from the joint presence of hydrophilic poly((RS)-3,3-dimethylmalic
The bacterial degradation of pantothenic acid. IV. Enzymatic conversion of aldopantoate to alpha-ketoisovalerate.
P T Magee et al.
Biochemistry, 5(2), 409-416 (1966-02-01)
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 61932-50MG | 04061833238257 |
| 61932-10MG | 04061833238240 |