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TETRADECANOIC-13,13,14,14,14-D5 ACID, with the CAS number 327077-03-2, is an isotopically labeled research compound that is utilized in various scientific studies and experiments. Its unique isotopic labeling allows for the tracking and analysis of specific biochemical processes and pathways.

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  • 327077-03-2 Structure
  • Basic information

    1. Product Name: TETRADECANOIC-13,13,14,14,14-D5 ACID
    2. Synonyms: TETRADECANOIC-13,13,14,14,14-D5 ACID;Tetradecanoic Acid-13,13,14,14,14-D5;Myristic acid-13,13,14,14,14-d5;Tetradecanoic-d5 Acid
    3. CAS NO:327077-03-2
    4. Molecular Formula: C14H23D5O2
    5. Molecular Weight: 233.4
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 327077-03-2.mol
  • Chemical Properties

    1. Melting Point: 52-54 °C(lit.)
    2. Boiling Point: 250 °C/100 mmHg(lit.)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: TETRADECANOIC-13,13,14,14,14-D5 ACID(CAS DataBase Reference)
    10. NIST Chemistry Reference: TETRADECANOIC-13,13,14,14,14-D5 ACID(327077-03-2)
    11. EPA Substance Registry System: TETRADECANOIC-13,13,14,14,14-D5 ACID(327077-03-2)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany: 3
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 327077-03-2(Hazardous Substances Data)

327077-03-2 Usage

Uses

Used in Research and Development:
TETRADECANOIC-13,13,14,14,14-D5 ACID is used as a research compound for the study of various biological and chemical processes. Its isotopic labeling enables researchers to trace and analyze specific pathways and interactions within complex biological systems.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, TETRADECANOIC-13,13,14,14,14-D5 ACID is used as a tool for drug discovery and development. Its isotopic labeling allows for the identification and characterization of potential drug targets, as well as the evaluation of drug efficacy and safety.
Used in Diagnostic Applications:
TETRADECANOIC-13,13,14,14,14-D5 ACID is employed in the development of diagnostic tools and tests, particularly in the field of medical imaging. Its isotopic labeling can help in the detection and monitoring of specific diseases or conditions, contributing to the advancement of personalized medicine.
Used in Environmental Studies:
TETRADECANOIC-13,13,14,14,14-D5 ACID can be utilized in environmental research to study the behavior and impact of various compounds in ecosystems. Its isotopic labeling allows for the tracking of pollutants and other substances, aiding in the understanding of their effects on the environment and the development of mitigation strategies.
Used in Forensic Science:
In forensic science, TETRADECANOIC-13,13,14,14,14-D5 ACID can be employed as a tracer compound to analyze and identify specific substances in criminal investigations. Its isotopic labeling can help in the detection and characterization of evidence, contributing to the resolution of cases and the administration of justice.

Check Digit Verification of cas no

The CAS Registry Mumber 327077-03-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,2,7,0,7 and 7 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 327077-03:
(8*3)+(7*2)+(6*7)+(5*0)+(4*7)+(3*7)+(2*0)+(1*3)=132
132 % 10 = 2
So 327077-03-2 is a valid CAS Registry Number.

327077-03-2Downstream Products

327077-03-2Relevant articles and documents

Penta-deuterated acid precursors in the pheromone biosynthesis of the Egyptian armyworm, Spodoptera littoralis

Munoz, Lourdes,Rosell, Gloria,Guerrero, Angel

experimental part, p. 493 - 498 (2010/08/06)

Synthesis of penta-deuterated intermediate precursors d5(E)-11-14:Acid (7), d5(Z)-11-14:Acid (10) and d514:Acid (12) of the pheromone of the Egyptian armyworm Spodoptera littoralis has been accomplished by a very convenient route starting from the commerc

Total synthesis of perdeuterated phospholipids

Bersch, B.,Starck, J. P.,Milon, A.,Nakatani, Y.,Ourisson, G.

, p. 575 - 583 (2007/10/02)

A general method for the total synthesis of various perdeuterated phospholipids (DMPA, DMPG, DMPE, DMPC) is described.Starting from simple and easily obtainable deuterated precursors, perdeuterated phosphatidic acid (DMPA-d59) was synthesized.DMPA-d59 was coupled to various perdeuterated alcohols in the presence of alkylsulfonyl chlorides as condensing agents.The preparation of the perdeuterated alcohols is also presented.The major advantage of this method lies in the independent synthesis of DMPA and the alcohol moieties, allowing the transformation to the desired phospholipid class in the final reaction step.The reaction scheme presented here can also be used for the synthesis of selectively deuterated phospholipids.Keywords - perdeuterated phospholipids / phosphatidic acid-d59 / phosphatidylglycerol-d64 / phosphatidylcholine-d72 / phopshatidylethanolamine-d63 / total synthesis

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