| Identification | More | [Name]
Cyclobutanecarboxylic acid | [CAS]
3721-95-7 | [Synonyms]
CYCLOBUTANECARBOXYLIC ACID
CYCLO-BUTYL FORMIC ACID
RARECHEM AL BO 0291
Cyclobutylcarboxylic acid
cyclobutylcarboxylicacid
Cyclobutanecarbonyl acid
cyclobutane carboyxlic acid
CYCLOBUTANOIC ACID 98% (GC)
CYCLOBUTANECARBOXYLIC AICD
CyclobutanecarboxylicAcid98%
cyclobutancecarboxylic acid
Cyclobutane-1-carboxylic acid | [EINECS(EC#)]
223-072-7 | [Molecular Formula]
C5H8O2 | [MDL Number]
MFCD00001323 | [Molecular Weight]
100.12 | [MOL File]
3721-95-7.mol |
| Safety Data | Back Directory | [Hazard Codes ]
Xi | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S23:Do not breathe gas/fumes/vapor/spray (appropriate wording to be specified by the manufacturer) .
S24/25:Avoid contact with skin and eyes .
S36:Wear suitable protective clothing .
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice . | [RIDADR ]
3265 | [WGK Germany ]
3
| [RTECS ]
GU1335000
| [F ]
13 | [TSCA ]
T | [HazardClass ]
8 | [PackingGroup ]
III | [HS Code ]
29162000 |
| Hazard Information | Back Directory | [Chemical Properties]
CLEAR COLOURLESS TO SLIGHTLY AMBER LIQUID | [Uses]
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. | [Preparation]
Cyclobutanecarboxylic 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 Methods]
Dissolve 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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