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3-Hydroxy-2,2,4,4-tetramethylcyclobutanone is a synthetic organic compound with the molecular formula C9H16O2. It is a colorless to pale yellow liquid with a molecular weight of 156.22 g/mol. 3-hydroxy-2,2,4,4-tetramethylcyclobutanone is characterized by its cyclobutanone ring structure, which is a four-membered cyclic ketone, and the presence of four methyl groups (CH3) attached to the carbon atoms at positions 2, 2, 4, and 4. The hydroxyl group (-OH) is attached to the carbon atom at position 3. This chemical is primarily used as a fragrance ingredient in the perfumery industry, providing a musky odor profile. It is also known for its use in the synthesis of other compounds and as a chemical intermediate in various industrial processes. Due to its potential health and environmental impacts, it is important to handle 3-hydroxy-2,2,4,4-tetramethylcyclobutanone with care and in accordance with safety regulations.

4916-59-0

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4916-59-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4916-59-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,9,1 and 6 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 4916-59:
(6*4)+(5*9)+(4*1)+(3*6)+(2*5)+(1*9)=110
110 % 10 = 0
So 4916-59-0 is a valid CAS Registry Number.

4916-59-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-hydroxy-2,2,4,4-tetramethylcyclobutan-1-one

1.2 Other means of identification

Product number -
Other names 3-Hydroxy-2,2,4,4-tetramethylcyclobutanone

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:4916-59-0 SDS

4916-59-0Relevant academic research and scientific papers

CATALYST AND METHOD FOR HYDROGENATION OF 1,3-CYCLOBUTANEDIKETONE COMPOUND

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Paragraph 0024; 00025, (2017/12/27)

Catalyst for hydrogenation of 1,3-cyclobutanediketone compound is provided, which includes a support and VIIIB group transition metal loaded thereon. The support includes a first oxide powder with a surface wrapped by a second oxide. The first oxide includes silicon oxide, aluminum oxide, zirconium oxide, titanium oxide, zinc oxide, or a combination thereof. The second oxide has a composition of MxAl(1-x)O(3-x)/2, M is alkaline earth metal, and x is from 0.3 to 0.7.

PROCESS FOR THE PREPARATION OF TETRAALKYLCYCLOBUTANE-1,3-DIOL IN THE PRESENCE OF A COBALT-BASED CATALYST

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Page/Page column 9-11, (2008/12/05)

The present invention relates to the production of 2,2,4,4-tetramethylcyclobutane-1,3-diol. In one embodiment, the present invention relates to the production of 2,2,4,4-tetramethylcyclobutane-1,3-diol by hydrogenation of 2,2,4,4-tetramethylcyclobutane-1,3-dione in the presence of a cobalt-based catalyst.

PROCESS FOR THE PREPARATION OF A TETRAALKYCYCLOBUTANE-1,3-DIOL USING A PROMOTED-COPPER CATALYST

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Page/Page column 16-18, (2008/12/05)

The present disclosure relates to the production of 2,2,4,4-tetraalkylcyclobutane-1,3-diol. In one embodiment, the present invention relates to the production of 2,2,4,4-tetraalkylcyclobutane-1,3-diol by hydrogenation of 2,2,4,4-tetraalkylcyclobutane-1,3-dione in the presence of a promoted copper-based catalyst.

PROCESS FOR THE PREPARATION OF A TETRAALKYLCYCLOBUTANE-1,3-DIOL USING AN IRIDIUM-PROMOTED COBALT-BASED CATALYST

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Page/Page column 10-11, (2008/12/05)

The present disclosure relates to the production of a 2,2,4,4-tetraalkylcyclobutane-1,3-diol. In one embodiment, the present invention relates to the production of a 2,2,4,4-tetraalkylcyclobutane-1,3-diol by hydrogenation of a 2,2,4,4-tetraalkylcyclobutane-1,3-dione in the presence of an iridium-promoted cobalt-based catalyst.

PROCESS FOR THE PREPARATION OF A TETRAALKYLCYCLOBUTANE-1,3-DIOL USING A PROMOTED NICKEL-BASED CATALYST

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Page/Page column 10-11, (2008/12/05)

The present invention relates to the production of a 2,2,4,4-tetraalkylcyclobutane-1,3-diol. In one embodiment, the present invention relates to the production of a 2,2,4,4-tetraalkylcyclobutane-1,3-diol by hydrogenation of a 2,2,4,4-tetraalkylcyclobutane-1,3-dione in the presence of a promoted nickel-based catalyst.

PROCESS FOR THE PREPARATION OF A TETRAALKYLCYCLOBUTANE-1,3-DIOL USING AN RUTHENIUM-PROMOTED COBALT-BASED CATALYST

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Page/Page column 10-11, (2008/12/06)

The present disclosure relates to the production of a 2,2,4,4-tetraalkylcyclobutane-1,3-diol. In one embodiment, the present invention relates to the production of a 2,2,4,4-tetraalkylcyclobutane-1,3-diol by hydrogenation of a 2,2,4,4-tetraalkylcyclobutane-1,3-dione in the presence of a ruthenium-promoted cobalt-based catalyst.

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