Levodopa EP Impurity D

Product Name Levodopa EP Impurity D
Alternate Names Levodopa Impurities, Impurities of Levodopa
CAT No. CS-O-10846
CAS No. 5796-17-8
Category Impurities
Stock IN-Stock
Mol. Wt. 197.19 g/mol
Mol. For. C₉H₁₁NO₄
Hazardous This is a Hazardous Compound
COA View Sample COA
MSDS View Sample MSDS
Parent API Levodopa
Purity >98%
Smileys N[C@@H](C(O)=O)CC1=CC(O)=C(O)C=C1
Canonical Smiles C1=CC(=C(C=C1CC(C(=O)O)N)O)O
InchIKey WTDRDQBEARUVNC-ZCFIWIBFSA-N
Inchl InChI=1S/C9H11NO4/c10-6(9(13)14)3-5-1-2-7(11)8(12)4-5/h1-2,4,6,11-12H,3,10H2,(H,13,14)/t6-/m1/s1
IUPAC (2R)-2-amino-3-(3,4-dihydroxyphenyl)propanoic acid
Controlled No
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Levodopa EP impurity D is a chemical compound that is used as an analytical standard and reference material in the pharmaceutical industry. It is a derivative of Levodopa, which is a medication used to treat Parkinson's disease. Levodopa EP impurity D is one of the many impurities that can be found in Levodopa, and its presence can affect the purity and quality of the medication. Chemically, Levodopa EP impurity D is known as 3,4-Dihydroxyphenylacetaldehyde. It is a yellow to brownish-yellow crystalline powder that is soluble in water and ethanol. Its molecular formula is C8H8O3 and its molecular weight is 152.15 g/mol. Levodopa EP impurity D is used in the analysis and identification of impurities in Levodopa. It is also used in research and development of new drugs that target the same neurological pathways as Levodopa. The presence of impurities in pharmaceuticals can affect the efficacy and safety of the medication, which is why Levodopa EP impurity D is an important tool in the quality control process. In conclusion, Levodopa EP impurity D is a useful reference material for the pharmaceutical industry. Its chemical properties and usage make it a valuable tool for ensuring the purity and quality of Levodopa and other medications that target the same neurological pathways.

Related Compounds

Levodopa Related Compound A |

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