4,4,4-Trifluoro-1-(2-thienyl)-1,3-butanedione TCI T0438

Chemical Identity

CAS No.: 326-91-0
PubChem: CID 5601·SID 87576390
Formula: C8H5F3O2S
Molecular weight: 222.19 g/mol
Purity: >98.0%(GC)
Reference databases: ChEBI·ChemSpider·ECHA·Wikipedia

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: 4,4,4-trifluoro-1-thiophen-2-ylbutane-1,3-dione
SMILES: C1=CSC(=C1)C(=O)CC(=O)C(F)(F)F
InChIKey: TXBBUSUXYMIVOS-UHFFFAOYSA-N

Rp 1.618.050,00

~~Rp 1.146.600,00~~ Rp 1.618.050,00

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Berat 25g 500g

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4,4,4-Trifluoro-1-(2-thienyl)-1,3-butanedione is a specialized chemical compound used as a building block in the synthesis of complex organic molecules. This compound plays a crucial role in laboratory settings where researchers aim to develop new materials, pharmaceuticals, or functional chemicals. Its unique molecular structure, featuring three fluorine atoms attached to a carbon backbone, makes it an essential tool for creating compounds with tailored reactivity and functional group compatibility. Due to its versatility, it is widely used in both academic and industrial research environments.

The compound’s fluorinated structure and presence of a thienyl group contribute to its high reactivity and ability to participate in various chemical reactions, such as nucleophilic and electrophilic substitutions. These properties make it particularly valuable for synthesizing heterocyclic compounds and organofluorine derivatives. Its stability under controlled conditions also enhances its usability in laboratory applications, allowing for reliable and reproducible results. This combination of reactivity and stability ensures that it remains a preferred choice for chemists working on advanced synthetic routes.

In Indonesian laboratories, this compound is commonly used in research focused on organic synthesis, drug development, and materials science. Its availability through suppliers like AMI Scientific ensures that local researchers have access to high-quality reagents for their experiments. The compound’s role in creating complex chemical structures makes it an indispensable resource for those working in advanced chemical research. Its consistent performance and reliability further support its widespread use in various scientific fields.

TCI brochures (PDF)

Metal Extractants for Lithium Ion Battery Recycling 2024-01-16 · p. 1
Thiophenes 2026-06-29 · p. 8
Ligands 2025-12-01 · p. 18

Related TCI products

Organic synthesis: This compound is widely used in the synthesis of complex organic molecules due to its reactivity and structural versatility.
Drug development: It serves as a key intermediate in the creation of pharmaceutical compounds, especially those requiring fluorinated functional groups.
Materials science: The compound is utilized in the development of advanced materials with specific chemical and physical properties.
Heterocyclic chemistry: Its thienyl group makes it ideal for synthesizing heterocyclic compounds with unique chemical behavior.
Fluorinated compound research: It is a preferred building block for studying the properties and applications of organofluorine compounds.

From the TCI brochure

Metal extractant for lithium ion battery recycling

Brand	TCI
CAS number	326-91-0
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Fluorinated Building Blocks
Pack sizes	Available in various quantities as per supplier specifications
Physical form	Solid or liquid, depending on supplier packaging
Storage	Store in a cool, dry place away from light and moisture

Data from the TCI brochure

Ukuran kemasan	25g / 500g

Source: TCI brochure FF164 (2024-01-16)

This compound should be stored in a cool, dry place, away from direct light and moisture to maintain its stability and prevent degradation. It is recommended to use suitable containers such as glass or high-density polyethylene to minimize chemical interactions. Due to its reactivity, it should be handled with care in a well-ventilated laboratory environment. Proper personal protective equipment, including gloves and safety goggles, should be worn during handling. The compound should not be exposed to incompatible substances, and all safety protocols should be followed to ensure safe laboratory practices.

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