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Sigma-Aldrich

10,12-Tricosadiynoic acid

≥98.0% (GC)

Sinonimo/i:

Tricosa-10,12-diynoic acid

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About This Item

Formula empirica (notazione di Hill):
C23H38O2
Numero CAS:
Peso molecolare:
346.55
Beilstein:
1880414
Numero MDL:
Codice UNSPSC:
12352100
ID PubChem:
NACRES:
NA.22

Saggio

≥98.0% (GC)

Forma fisica

crystals

Condizioni di stoccaggio

protect from light

Punto di fusione

56-60 °C

Stringa SMILE

CCCCCCCCCCC#CC#CCCCCCCCCC(O)=O

InChI

1S/C23H38O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22-23(24)25/h2-10,15-22H2,1H3,(H,24,25)
DIEDVCMBPCRJFQ-UHFFFAOYSA-N

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Descrizione generale

10,12-Tricosadiynoic acid, also known as Tricosa-10,12-diynoic acid, is a monomeric amphiphilic diacetylene fatty acid characterized by long paraffinic chains on both sides of the diacetylene moiety. This compound is often used in the synthesis of polymerizable monolayers and Langmuir-Blodgett multilayers.

Applicazioni

  • Acid-responsive color transition in polymer assemblies: 10,12-Tricosadiynoic acid is employed in the development of acid-responsive polydiacetylene-Na(+) assemblies, showcasing a unique red-to-blue color transition. This property is significant for applications in smart sensors and visual indicators in various industrial processes (Saymung et al., 2024).
  • Colorimetric sensing capabilities: The synthesis of polydiacetylene vesicles incorporating 10,12-Tricosadiynoic acid demonstrates their utility as colorimetric sensors. This application is particularly valuable in the detection of microbial peptides, contributing to advancements in food safety and pharmaceutical analysis (Yadav and Tiwari, 2021).

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

Eyeshields, Gloves, type N95 (US)


Certificati d'analisi (COA)

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We have demonstrated colorimetric and fluorescence detection of a peptide, melittin, based on polydiacetylene (PDA) made of 1,2-bis(10,12-tricosadiynoyl)-sn-glycero-3-phosphocholine (DC(8,9)PC). The PDA used in this work has a phosphocholine headgroup, which mimics peptide-cell membrane interactions better than the conventional PDAs with
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