Cyclobutanecarboxylic acid
Cyclobutanecarboxylic acid
  • CAS No.:3721-95-7
Other grades of this product :
Cyclobutanecarboxylic acid Basic information
Product Name:Cyclobutanecarboxylic acid
Synonyms:RARECHEM AL BO 0291;CYCLO-BUTYL FORMIC ACID;Cyclobutylcarboxylic acid;cyclobutylcarboxylicacid;Cyclobutanecarbonyl acid;cyclobutane carboyxlic acid;CYCLOBUTANOIC ACID 98% (GC);CYCLOBUTANECARBOXYLIC AICD
CAS:3721-95-7
MF:C5H8O2
MW:100.12
EINECS:223-072-7
Product Categories:Aromatic Carboxylic Acids, Amides, Anilides, Anhydrides & Salts;Acids and Derivatives;Cyclobutanes & Cyclobutenes;Simple 4-Membered Ring Compounds;Cycloalkanes;C1 to C5;Carbonyl Compounds;Carboxylic Acids;bc0001
Mol File:3721-95-7.mol
Cyclobutanecarboxylic acid Chemical Properties
Melting point −7.5 °C(lit.)
Boiling point 195 °C(lit.)
density 1.047 g/mL at 25 °C(lit.)
refractive index n20/D 1.444(lit.)
Fp 183 °F
storage temp. Sealed in dry,Room Temperature
form Liquid
pkapK1:4.785 (25°C)
Specific Gravity1.047
color Clear colorless to yellow
Water Solubility Slightly soluble in water.
BRN 1816777
CAS DataBase Reference3721-95-7(CAS DataBase Reference)
NIST Chemistry ReferenceCyclobutane carboxylic acid(3721-95-7)
EPA Substance Registry SystemCyclobutanecarboxylic acid (3721-95-7)
Safety Information
Hazard Codes Xi,C
Risk Statements 36/37/38-34-20/21/22
Safety Statements 23-24/25-36-26-45-36/37/39
RIDADR 3265
WGK Germany 3
RTECS GU1335000
13
TSCA T
HazardClass 8
PackingGroup III
HS Code 29162000
MSDS Information
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Cyclobutanecarboxylic acid Usage And Synthesis
Chemical PropertiesCLEAR COLOURLESS TO SLIGHTLY AMBER LIQUID
UsesCyclobutanecarboxylic 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.
PreparationCyclobutanecarboxylic acid synthesis: Put 1,1-Cyclobutanedicarboxylic acid into a distillation device for heating, decarboxylate at about 160°C to release carbon dioxide, then heat for distillation, collect 189-195°C fractions as crude product, and re-distill to obtain the finished product cyclobutanecarboxylic acid. Yield 86%-91%.
Synthesis Reference(s)The Journal of Organic Chemistry, 22, p. 1680, 1957 DOI: 10.1021/jo01363a041
Purification MethodsDissolve the acid in aqueous HCO 3 then acidify with HCl and extract it into Et2O, wash with H2O, dry (Na2SO4), concentrate to a small volume, then distil it through a glass helices packed column. The S-benzylisothiuronium salt has m 176o (from EtOH), the anilide has m 112.5-113o, and the p-toluide has m 123o. [Payne & Smith J Org Chem 22 1680 1957, Kantaro & Gunning J Am Chem Soc 73 480 1951, Stodola & Heisig Org Synth Coll Vol III 213 1955, Beilstein 9 H 5.]

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