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5,7-Dodecadiynedioic acid, also known as 5,7-dodecadiynedioic acid or DDDA, is a chemical compound with the molecular formula C12H14O4. It is a diacetylenic acid with alkyne functional groups, which give it unique properties and make it suitable for a variety of applications.

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  • 28393-04-6 Structure
  • Basic information

    1. Product Name: 5,7-DODECADIYNEDIOIC ACID
    2. Synonyms: 5,7-DODECADIYNEDIOIC ACID;5,7-DODECADIYNDIOIC ACID;TIMTEC-BB SBB008729;5,7-DODECADIYNEDIOIC ACID 98%
    3. CAS NO:28393-04-6
    4. Molecular Formula: C12H14O4
    5. Molecular Weight: 222.24
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 28393-04-6.mol
  • Chemical Properties

    1. Melting Point: 142 °C
    2. Boiling Point: 494.6 °C at 760 mmHg
    3. Flash Point: 267 °C
    4. Appearance: /
    5. Density: 1.217 g/cm3
    6. Vapor Pressure: 3.94E-11mmHg at 25°C
    7. Refractive Index: 1.534
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 5,7-DODECADIYNEDIOIC ACID(CAS DataBase Reference)
    11. NIST Chemistry Reference: 5,7-DODECADIYNEDIOIC ACID(28393-04-6)
    12. EPA Substance Registry System: 5,7-DODECADIYNEDIOIC ACID(28393-04-6)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: 22-24/25
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 28393-04-6(Hazardous Substances Data)

28393-04-6 Usage

Uses

Used in Polymer and Resin Production:
5,7-Dodecadiynedioic acid is used as a monomer for the production of high-performance polymers and resins. Its ability to undergo polymerization reactions allows for the creation of materials with high thermal stability, mechanical strength, and resistance to harsh environments.
Used in Specialty Chemical Synthesis:
5,7-Dodecadiynedioic acid is used as a starting material in the synthesis of specialty chemicals. Its unique chemical structure and properties make it a valuable component in the development of new chemical compounds.
Used in Electronics Industry:
5,7-Dodecadiynedioic acid has potential applications in the electronics industry due to its unique chemical structure and properties. It can be used in the development of advanced materials for electronic devices and components.
Used in Aerospace Industry:
5,7-Dodecadiynedioic acid can be used in the aerospace industry for the production of materials with high thermal stability and mechanical strength, making it suitable for use in aircraft and spacecraft components.
Used in Biomedicine:
5,7-Dodecadiynedioic acid has potential applications in the field of biomedicine due to its unique chemical structure and properties. It can be used in the development of new medical materials and devices, as well as in the synthesis of pharmaceutical compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 28393-04-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,3,9 and 3 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 28393-04:
(7*2)+(6*8)+(5*3)+(4*9)+(3*3)+(2*0)+(1*4)=126
126 % 10 = 6
So 28393-04-6 is a valid CAS Registry Number.
InChI:InChI=1/C12H14O4/c13-11(14)9-7-5-3-1-2-4-6-8-10-12(15)16/h5-10H2,(H,13,14)(H,15,16)

28393-04-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name dodeca-5,7-diynedioic acid

1.2 Other means of identification

Product number -
Other names Dodeca-5,7-diindisaeure

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:28393-04-6 SDS

28393-04-6Relevant articles and documents

Use of Imidazo[1,5-a]pyridin-3-ylidene as a Platform for Metal-Imidazole Cooperative Catalysis: Silver-Catalyzed Cyclization of Alkyne-Tethered Carboxylic Acids

Rawat, Vishal Kumar,Higashida, Kosuke,Sawamura, Masaya

supporting information, p. 1631 - 1637 (2021/02/03)

Silver complexes with 5-(4-(tert-butyl)-1H-imidazol-1-yl)-imidazo[1,5-a]pyridin-3-ylidene ligands were synthesized as metal-imidazole acid-base cooperative catalysts. Single crystal XRD analysis revealed that the silver atom was located in the vicinity of

Self-assembly and solid-state polymerization of butadiyne derivatives with amide and trialkoxyphenyl groups

Kikuchi, Kohei,Tatewaki, Yoko,Okada, Shuji

, p. 298 - 305 (2017/05/10)

Three butadiyne derivatives with amide and tri(dodecyloxy)-phenyl (TDP) groups were synthesized, and four solidification methods were applied to obtain their self-assembling states in various conditions. The solids obtained were characterized by the solid-state polymerization behaviors, stretching vibration wavenumbers of N-H bonds of amide groups, powder X-ray diffraction, the thermal behaviors, and scanning electron microscope (SEM) observations. We found that all compounds had at least two polymorphs. Property differences between two polymorphs depended on the compounds. Two compounds showed clear differences in UV-vis spectra of the photo-polymerized solids, i.e., the polydiacetylene (PDA) structure, and irregularly polymerized form, or two PDA structures. The remaining compound showed the same PDA absorption but the monomer melting points were different. All compounds gave the gels in various organic solvents because of the molecular design with amide and TDP groups. SEM observation clarified the relationship between gel appearance and the nanostructures.

Polydiacetylene paper-based colorimetric sensor array for vapor phase detection and identification of volatile organic compounds

Eaidkong, Thichamporn,Mungkarndee, Radeemada,Phollookin, Chaiwat,Tumcharern, Gamonwarn,Sukwattanasinitt, Mongkol,Wacharasindhu, Sumrit

experimental part, p. 5970 - 5977 (2012/06/18)

Detection and identification of VOCs in their vapor phase is essential for safety and quality assessment. In this work, a novel platform of a paper-based polydiacetylene (PDA) colorimetric sensor array is prepared from eight diacetylene monomers, six of which are amphiphilic and the other two are bolaamphiphilic. To fabricate the sensors, monomers are coated onto a filter paper surface using the drop-casting technique and converted to PDAs by UV irradiation. The PDA sensors show solvent induced irreversible color transition upon exposure to VOC vapors. When combined into a sensing array, the color change pattern as measured by RGB values and statistically analyzed by principal component analysis (PCA) is capable of distinguishing 18 distinct VOCs in the vapor phase. The PCA score and loading plots also allow the reduction of the sensing elements in the array from eight to three PDAs that are capable of classifying 18 VOCs. Utilizing an array containing only two PDAs, various types of automotive fuels including gasoline, gasohol and diesel are successfully classified. The Royal Society of Chemistry 2012.

Cyclization of alkynoic acids with gold catalysts: a surprising dichotomy between AuI and AuIII

Harkat, Hassina,Dembelé, Albert Yénimégué,Weibel, Jean-Marc,Blanc, Aurélien,Pale, Patrick

experimental part, p. 1871 - 1879 (2009/06/28)

ω-Acetylenic acids, substituted or not at their acetylenic end, could be efficiently cyclized to γ- or δ-alkylidene lactones in the presence of AuCl and K2CO3. In contrast AuCl3 led to lactone dimers, probably through cycl

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