Cyclobutanecarboxylic acid, 97%
Cyclobutanecarboxylic acid, 97%
Cyclobutanecarboxylic acid, 97%
Thermo Scientific Chemicals

Cyclobutanecarboxylic acid, 97%

CAS: 3721-95-7 | C5H8O2 | 100.12 g/mol
数量:
5 g
25 g
100 g
製品番号(カタログ番号) A14480.14
または、製品番号A14480-14
価格(JPY)
-
数量:
25 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
CAS3721-95-7
IUPAC Namecyclobutanecarboxylic acid
Molecular FormulaC5H8O2
InChI KeyTXWOGHSRPAYOML-UHFFFAOYSA-N
SMILESOC(=O)C1CCC1
さらに表示
Appearance (Color)Clear colorless to pale yellow
Refractive Index1.4415-1.4455 @ 20?C
Assay (Aqueous acid-base Titration)≥98.0 to ≤102.0%
FormLiquid
Assay (Silylated GC)≥98.0%
Cyclobutanecarboxylic acid is used in water treatment, row materials for sodium fluosilicate potassium fluosilicateammonium fluosilicatecopper fluosilicatebarium fluosilicate and other fluosilicates and silicic tetrafluoride. It is also used in refining lead of electrolysis, as mordant and in the treatment of metal surface.

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
Cyclobutanecarboxylic acid is used in water treatment ,row materials for sodium fluosilicate potassium fluosilicateammonium fluosilicatecopper fluosilicatebarium fluosilicate and other fluosilicates and silicic tetrafluoride. It is also used in metal platingtimber antisepsisdisinfectant(1-2% of solution) of beer and brewing industry, refining lead of electrolysis, as mordant and in the treatment of metal surface.

Solubility
Slightly soluble in water.

Notes
Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Containers which are opened must be carefully resealed and kept upright to prevent leakage.
RUO – Research Use Only

General References:

  1. JAMES CASON.; CHARLES F. ALLEN. THE PREPARATION OF CYCLOBUTANECARBOXYLIC ACID. J. Org. Chem. 1949, 14 (6), 1036-1038.
  2. WILLIAM A. NEVILL.; DOROTHY SWENSON FRANK.; ROBERT D. TREPKA. Free Radical Chlorination of Cyclobutanecarboxylic Acids. J. Org. Chem. 1962, 27 (2), 422-428.
  3. ɑ-Alkyation of the dilithio-derivative is the first step in a route to 1,2-disubstituted cyclopentenes, and hence, by ozonolysis, 1,5-diketones: Synthesis, 603 (1984):