1,2,3,4-Butanetetracarboxylic acid, 98+%
1,2,3,4-Butanetetracarboxylic acid, 98+%
1,2,3,4-Butanetetracarboxylic acid, 98+%
Thermo Scientific Chemicals

1,2,3,4-Butanetetracarboxylic acid, 98+%

CAS: 1703-58-8 | C8H10O8 | 234.16 g/mol
製品番号(カタログ番号) A16612.36
または、製品番号A16612-36
価格(JPY)
-
数量:
500 g
一括またはカスタム形式をリクエストする
化学物質識別子
CAS1703-58-8
IUPAC Namebutane-1,2,3,4-tetracarboxylic acid
Molecular FormulaC8H10O8
InChI KeyGGAUUQHSCNMCAU-UHFFFAOYNA-N
SMILESOC(=O)CC(C(CC(O)=O)C(O)=O)C(O)=O
さらに表示
Assay (Silylated GC)≥98.0%
Appearance (Color)White
Assay (Aqueous acid-base Titration)≥98.0 to ≤102.0%
Identification (FTIR)Conforms
FormPowder
1,2,3,4-Butanetetracarboxylic acid is used as a cross linking agent to prepare cotton cellulose in order to improve anti-prilling and flame retardant properties. It is used as a spacer in the cross-linking of titania nanoparticles to cotton. Further, it is used as a nonformaldehyde durable press finishing agent.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
1,2,3,4-Butanetetracarboxylic acid is used as a cross linking agent to prepare cotton cellulose in order to improve anti-prilling and flame retardant properties. It is used as a spacer in the cross-linking of titania nanoparticles to cotton. Further, it is used as a nonformaldehyde durable press finishing agent.

Solubility
Soluble in water and ethanol.

Notes
Incompatible with strong oxidizing agents.
RUO – Research Use Only

General References:

  1. Ji, B.; Tang, P.; Yan, K.; Sun, G. Catalytic actions of alkaline salts in reactions between 1,2,3,4-butanetetracarboxylic acid and cellulose: II. Esterification. Carbohydr. Polym. 2015, 132, 228-236.
  2. Kawase, T.; Nomura, Y.; Oida, T. Synthesis and Properties of 1,2,3,4-Butanetetracarboxylic Acid Type Gemini Surfactants with Semifluoroalkyl Chain as Hydrophobic Group. Tenside Surfact. Det. 2014, 52 (5), 386-395.