Propionic Acid-d5 - ≥98 atom% D,≥98% , CAS No.60153-92-6

CAS: 60153-92-6 Cat. No.: P343294 Formula: C₃HD₅O₂ Peso molecolare: 79.11 Numero EC: 685-184-6

GRADE & PURITY ≥98 atom% D,≥98%

Synonyms

d5-propanoic acid | DTXSID60731121 | A935650 | Propionic-d5 acid | Propanoic-d5 acid | Propionic Acid-d5 | Propionic-d5 acid, >=98 atom % D, >=99% (CP) | (~2~H_5_)Propanoic acid | D99193 | (?H?)propanoic acid | 2,2,3,3,3-pentadeuteriopropanoic acid | Etha

Storage

Protected from light,Room temperature,Argon charged

Shipped In

Normal

Panoramica

Hyperpolarization, Metabolomics, MRI/MRS, MS/MS Standards, Synthetic Intermediates

Specifications

Sinonimi

d5-propanoic acid | DTXSID60731121 | A935650 | Propionic-d5 acid | Propanoic-d5 acid | Propionic Acid-d5 | Propionic-d5 acid, >=98 atom % D, >=99% (CP) | (~2~H_5_)Propanoic acid | D99193 | (?H?)propanoic acid | 2,2,3,3,3-pentadeuteriopropanoic acid | Etha

Specifiche e purezza

≥98 atom% D,≥98%

Condizioni di conservazione di stoccaggio

Protected from light,Room temperature,Argon charged

Spedito in

Normal

Purezza

≥98 atom% D,≥98%

Nomi e identificatori

• Pubchem Sid: 504771720
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504771720
• Sorrisi canonici: CCC(=O)O
• IUPAC Name: 2,2,3,3,3-pentadeuteriopropanoic acid
• InChIKey: XBDQKXXYIPTUBI-ZBJDZAJPSA-N
• INCHI: 1S/C3H6O2/c1-2-3(4)5/h2H2,1H3,(H,4,5)/i1D3,2D2
• Isomeri SMILES: [2H]C([2H])([2H])C([2H])([2H])C(=O)O
• CAS alternativo: 79-09-4(unlabelled)
• Peso molecolare: 79.11
• Reaxy-Rn: 506071
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=506071&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic acids and derivatives
    • Classe Carboxylic acids and derivatives
      • Subclass Carboxylic acids

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Classe: Carboxylic acids and derivatives
• Subclass: Carboxylic acids
• Intermediate Tree Nodes: Not available
• Direct Parent: Carboxylic acids
• Alternative Parents: Monocarboxylic acids and derivatives Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Monocarboxylic acid or derivatives - Carboxylic acid - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aliphatic acyclic compound
• Descrizione: This compound belongs to the class of organic compounds known as carboxylic acids. These are compounds containing a carboxylic acid group with the formula -C(=O)OH.
• External Descriptors: Not available

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Proprietà chimiche e fisiche

• Sensibilità: Moisture &light sensitive
• Peso molecolare: 79.110 g/mol
• XLogP3: 0.300
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 1
• Exact Mass: 79.0682 Da
• Monoisotopic Mass: 79.0682 Da
• Topological Polar Surface Area: 37.300 Ų
• Heavy Atom Count: 5
• Formal Charge: 0
• Complexity: 40.200
• Isotope Atom Count: 5
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1

Riferimenti

1. Haiyin Zhang, Haofang Wan, Yihang Lu, Yu He, Haitong Wan, Chang Li.  (2026)  Astragalus membranaceus—Salvia miltiorrhiza Decoction Ameliorates Metabolic Syndrome and Gut Microbiota Dysbiosis Induced by High‐Fat Diet: A Comparative Study.  Food Science & Nutrition,  14  (1): (e71436).  [PMID:41523274] [10.1002/fsn3.71436]