Description References
ChemicalBook > CAS DataBase List > Cyclobutanone

Cyclobutanone

Description References
Product Name
Cyclobutanone
CAS No.
1191-95-3
Chemical Name
Cyclobutanone
Synonyms
CBON;obutanone;CYCLOBUTANONE;Oxocyclobutane;1-Oxocyclobutane;Cyclobutanone 98%;Cyclobutanone, 98+%;OS-7558Cyclobutanone;cyclobutanone(SALTDATA: FREE);Cyclobutanone, 98%, stabilized
CBNumber
CB7231982
Molecular Formula
C4H6O
Formula Weight
70.09
MOL File
1191-95-3.mol
More
Less

Cyclobutanone Property

Melting point:
-50.9 °C
Boiling point:
99 °C (lit.)
Density 
0.938 g/mL at 25 °C (lit.)
refractive index 
n20/D 1.421(lit.)
Flash point:
50 °F
storage temp. 
2-8°C
solubility 
soluble in Dichloromethane
form 
Liquid
Specific Gravity
0.938
color 
Clear colorless to slightly yellow
Water Solubility 
INSOLUBLE
BRN 
1560289
Stability:
Volatile
InChIKey
SHQSVMDWKBRBGB-UHFFFAOYSA-N
CAS DataBase Reference
1191-95-3(CAS DataBase Reference)
EPA Substance Registry System
Cyclobutanone (1191-95-3)
More
Less

Safety

Hazard Codes 
F,F+
Risk Statements 
10-11
Safety Statements 
23-24/25-9-33-29-16-7/9
RIDADR 
UN 1224 3/PG 3
WGK Germany 
3
TSCA 
Yes
HazardClass 
3
PackingGroup 
II
HS Code 
29142900
More
Less

Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Danger
Hazard statements

H225Highly Flammable liquid and vapour

Precautionary statements

P210Keep away from heat/sparks/open flames/hot surfaces. — No smoking.

P233Keep container tightly closed.

P240Ground/bond container and receiving equipment.

P241Use explosion-proof electrical/ventilating/lighting/…/equipment.

P242Use only non-sparking tools.

P243Take precautionary measures against static discharge.

More
Less

N-Bromosuccinimide Price

Sigma-Aldrich
Product number
C96001
Product name
Cyclobutanone
Purity
99%
Packaging
1g
Price
$33.4
Updated
2024/03/01
Sigma-Aldrich
Product number
C96001
Product name
Cyclobutanone
Purity
99%
Packaging
5g
Price
$159
Updated
2024/03/01
TCI Chemical
Product number
C1913
Product name
Cyclobutanone (stabilized with Na2CO3)
Purity
>97.0%(GC)
Packaging
1g
Price
$55
Updated
2024/03/01
TCI Chemical
Product number
C1913
Product name
Cyclobutanone (stabilized with Na2CO3)
Purity
>97.0%(GC)
Packaging
5g
Price
$180
Updated
2024/03/01
Alfa Aesar
Product number
A13068
Product name
Cyclobutanone, 98%, stab. with ca 0.01% BHT
Packaging
1g
Price
$74.65
Updated
2024/03/01
More
Less

Cyclobutanone Chemical Properties,Usage,Production

Description

Cyclobutanone is an organic compound with a four-membered cyclic ketone. It is used in preparation of cyclobutane derivatives, as a starting material for aminocyclobutanecarboxylic acid through sulfonyloxiranes, to prepare dihydro-furan-2-one in presence of polystyrene-bound phenylselenic acid as catalyst. It is also involved in the photochemical synthesis of nucleoside analogues such as bicyclic nucleosides and isonucleosides. Furthermore, it is used to synthesis fatty acid, 2-oxo-cyclobutane undecanoic acid, which is used in the development of an enzyme-linked immunosorbent assy for the detection of irradiated foods.

References

[1] https://en.wikipedia.org/wiki/Cyclobutanone
[2] https://www.alfa.com/de/catalog/A13068/
[3] https://www.scbt.com/scbt/de/product/2-oxo-cyclobutane-undecanoic-acid-169263-77-8/;jsessionid=Ay2KMCxORq9y-EC6YoYnGGtCnymUGxQi5Lpd-YuCZoW22Re8Xf4w!-2072765631

Chemical Properties

Clear colourless to slightly yellow liquid

Uses

Cyclobutanone is used in preparation of cyclobutane derivatives. It is used as a starting material for aminocyclobutanecarboxylic acid through sulfonyloxiranes. It is also used to prepare dihydro-furan-2-one in presence of polystyrene-bound phenylselenic acid as catalyst. Further, it is involved in the photochemical synthesis of nucleoside analogues such as bicyclic nucleosides and isonucleosides.

Preparation

The Russian chemist Nikolai Kischner first prepared cyclobutanone in 1905. He synthesized cyclobutanone in a low yield from cyclobutanecarboxylic acid in several reaction steps.
Another synthesis of cyclobutanone involves lithium-catalyzed rearrangement of oxaspiropentane, which is formed by epoxidation of the easily accessible methylenecyclopropane.

Purification Methods

Treat cyclobutanone with dilute aqueous KMnO4, dry it with molecular sieves and fractionally distil it. Purify it via the semicarbazone, then regenerate the ketone, dry it (CaSO4), and distil it in a stainless steel spinning-band (or Vigreux, p 11) column. Alternatively, purify it by preparative gas chromatography using a Carbowax 20-M column at 80o. (This treatment also removes acetone). The oxime has m 84-85o (from pet ether) and the semicarbazone has m 212-212-5o (220-221o from MeOH or H2O, Buchanan et al. J Am Chem Soc 64 2701 1942). [Salaun Org Synth 57 36 1977, Fitzer & Quabeck Synthesis 299 1987, Beilstein 7 IV 3.]

Cyclobutanone Preparation Products And Raw materials

Raw materials

Preparation Products

More
Less

Cyclobutanone Suppliers

Pure Chemistry Scientific Inc.
Tel
001-857-928-2050 or 1-888-588-9418
Fax
001-617-206-9595
Email
sales@chemreagents.com
Country
United States
ProdList
10186
Advantage
62
HBCChem, Inc.
Tel
+1-510-219-6317
Fax
+1-650-486-1361
Email
sales@hbcchem.com
Country
United States
ProdList
10648
Advantage
60
Accela ChemBio Inc.
Tel
+1-858-6993322
Fax
(+1)-858-876-1948
Email
info@accelachem.com
Country
United States
ProdList
17982
Advantage
58
Aladdin Scientific
Tel
+1-+1(833)-552-7181
Email
sales@aladdinsci.com
Country
United States
ProdList
57505
Advantage
58
Aceschem Inc.
Tel
+1-817863-6948 +1-(817)863-6948
Email
sales@aceschem.com
Country
United States
ProdList
19632
Advantage
58
Fluorochem Ltd.
Tel
--
Fax
--
Email
enquiries@fluorochem.co.uk
Country
United States
ProdList
4583
Advantage
58
Combi-Blocks, Inc.
Tel
--
Fax
--
Email
les@combi-blocks.com
Country
United States
ProdList
2555
Advantage
58
Alichem Inc.
Tel
--
Fax
--
Email
sales@alichem.com
Country
United States
ProdList
6167
Advantage
58
MilliporeSigma (Sigma-Aldrich Corp.)
Tel
--
Fax
--
Email
@sial.com
Country
United States
ProdList
5414
Advantage
58
Oakwood Products, Inc.
Tel
--
Fax
--
Email
sales@oakwoodchemical.com
Country
United States
ProdList
6193
Advantage
74
OChem Incorporation
Tel
--
Fax
--
Email
sales@ocheminc.com
Country
United States
ProdList
6501
Advantage
60
VWR International, LLC.
Tel
--
Fax
--
Email
@sargentwelch.com
Country
United States
ProdList
6262
Advantage
58
HBCChem Inc.
Tel
--
Fax
--
Email
sales@hbcchem-inc.com
Country
United States
ProdList
4569
Advantage
30
United States Biological
Tel
--
Fax
--
Email
chemicals@usbio.net
Country
United States
ProdList
6214
Advantage
80
SynQuest Laboratories, Inc.
Tel
--
Fax
--
Email
info@synquestlabs.com
Country
United States
ProdList
6871
Advantage
62
Riedel-de Haen AG
Tel
--
Fax
--
Country
United States
ProdList
6773
Advantage
87
TCI America
Tel
--
Fax
--
Email
sales@tciamerica.com
Country
United States
ProdList
6909
Advantage
75
Frontier Scientific, Inc.
Tel
--
Fax
--
Email
sales@frontiersci.com
Country
United States
ProdList
6222
Advantage
86
Matrix Scientific
Tel
--
Fax
--
Email
sales@matrixscientific.com
Country
United States
ProdList
6632
Advantage
80
Anvia Chemicals, LLC
Tel
--
Fax
--
Email
sales@anviachem.com
Country
United States
ProdList
3933
Advantage
0
Wilshire Chemical Company Inc.
Tel
--
Fax
--
Email
WilshrChem@AOL.COM
Country
United States
ProdList
3498
Advantage
58
Waterstone Technology, LLC
Tel
--
Fax
--
Email
sales@waterstonetech.com
Country
United States
ProdList
6786
Advantage
30
AlliChem, LLC
Tel
--
Fax
--
Email
sales@allichemllc.com
Country
United States
ProdList
6516
Advantage
60
Combi-Blocks Inc.
Tel
--
Fax
--
Email
sales@combi-blocks.com
Country
United States
ProdList
6618
Advantage
69
Anthem Pharmaceutical Research LLC
Tel
--
Fax
--
Email
sales@anthempharma.com
Country
United States
ProdList
3040
Advantage
30
AstaTech, Inc
Tel
--
Fax
--
Email
sales@astatechinc.com
Country
United States
ProdList
6371
Advantage
58
ChemSampCo, Inc.
Tel
--
Fax
--
Email
sales@chemsampco.com
Country
United States
ProdList
3585
Advantage
60
AK Scientific, Inc.
Tel
--
Fax
--
Email
sales@aksci.com
Country
United States
ProdList
6347
Advantage
65
Alfa Aesar
Tel
--
Fax
--
Email
tech@alfa.com
Country
United States
ProdList
6814
Advantage
81
HONEST JOY HOLDINGS LIMITED
Tel
--
Fax
--
Email
sales@honestjoy.cn
Country
United States
ProdList
6675
Advantage
54
APAC Pharmaceutical, LLC
Tel
--
Fax
--
Email
sales@apacpharma.com
Country
United States
ProdList
6322
Advantage
38
ChemPacific Corporation
Tel
--
Fax
--
Email
sales@chempacific.com
Country
United States
ProdList
6891
Advantage
51
More
Less

View Lastest Price from Cyclobutanone manufacturers

Hebei Chuanghai Biotechnology Co,.LTD
Product
Cyclobutanone 1191-95-3
Price
US $5.00-2.00/KG
Min. Order
1KG
Purity
99%
Supply Ability
10000kg
Release date
2024-08-19
Hangzhou ICH Biofarm Co., Ltd
Product
Cyclobutanone 1191-95-3
Price
US $0.00-0.00/kg
Min. Order
0.10000000149011612kg
Purity
99.0%min
Supply Ability
200kg
Release date
2023-07-03
Zhuozhou Wenxi import and Export Co., Ltd
Product
Cyclobutanone 1191-95-3
Price
US $15.00-10.00/KG
Min. Order
1KG
Purity
99%+ HPLC
Supply Ability
Monthly supply of 1 ton
Release date
2021-07-10

1191-95-3, CyclobutanoneRelated Search:


  • CBON
  • CYCLOBUTANONE
  • Cyclobutanone, 98+%
  • Cyclobutanone 98%
  • Cyclobutanone, 98%, stab. with ca 0.01% BHT
  • Oxocyclobutane
  • Cyclobutanone (stabilized with Na2CO3)
  • Cyclobutanone, 98%, stabilized
  • OS-7558Cyclobutanone
  • Cyclobutanone, Stab. With ca 0.01% Bht
  • cyclobutanone(SALTDATA: FREE)
  • 1-Oxocyclobutane
  • CYCLOBUTANONE FOR SYNTHESIS 1 ML
  • CYCLOBUTANONE FOR SYNTHESIS 5 ML
  • Cyclobutanone, stabilized with &ap:0.01% BHT
  • obutanone
  • Cyclobutanone - stabilise 0.01 % BHT
  • Cyclobutanone (stabilized with Na2CO3)&gt
  • Cyclobutanone(For export only)
  • Cyclobutanone, stab. with 0.1% BHT
  • Cyclobutanone (6CI, 8CI, 9CI, ACI)
  • 1191-95-3
  • C4H60
  • Ketones
  • Organic Building Blocks
  • C3 to C6
  • Carbonyl Compounds
  • Building Blocks
  • Cyclobutanes & Cyclobutenes
  • Simple 4-Membered Ring Compounds
  • C3 to C6
  • Carbonyl Compounds
  • Ketones
  • ketone
  • Carbonyl Compounds
  • Pharmaceutical Intermediates
  • cyclic compounds
  • bc0001
  • 1191-95-3