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3010-96-6

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3010-96-6 Usage

Chemical Properties

white crystalline powder

Uses

Different sources of media describe the Uses of 3010-96-6 differently. You can refer to the following data:
1. Chemical intermediate, lubricants.
2. 2,2,4,4-Tetramethyl-1,3-cyclobutanediol was used in the preparation of Eastman Tritan? copolyester.

Flammability and Explosibility

Nonflammable

Check Digit Verification of cas no

The CAS Registry Mumber 3010-96-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,0,1 and 0 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 3010-96:
(6*3)+(5*0)+(4*1)+(3*0)+(2*9)+(1*6)=46
46 % 10 = 6
So 3010-96-6 is a valid CAS Registry Number.
InChI:InChI=1/C8H16O2/c1-7(2)5(9)8(3,4)6(7)10/h5-6,9-10H,1-4H3

3010-96-6 Well-known Company Product Price

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  • (Code)Product description
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  • Aldrich

  • (131946)  2,2,4,4-Tetramethyl-1,3-cyclobutanediol,mixtureofisomers  99%

  • 3010-96-6

  • 131946-10G

  • 1,519.83CNY

  • Detail

3010-96-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2,4,4-TETRAMETHYL-1,3-CYCLOBUTANEDIOL

1.2 Other means of identification

Product number -
Other names 2,2,4,4-tetramethylcyclobutane-1,3-diol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Intermediates
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:3010-96-6 SDS

3010-96-6Relevant articles and documents

Preparation method of 2, 2, 4, 4-tetramethyl-1, 3-cyclobutanediol

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Paragraph 0014; 0027; 00289-0030; 0032-0033; 0035-0036; 0038, (2021/03/11)

The invention discloses a preparation method of 2, 2, 4, 4-tetramethyl-1, 3-cyclobutanediol, which comprises the following steps: dissolving isobutyryl chloride in a first organic solvent, adding triethylamine and zinc powder while stirring, heating to reflux, reacting, cooling, filtering, washing, and carrying out reduced pressure distillation to obtain a distillation substrate; and dissolving the distillation substrate in a second organic solvent, cooling, filtering, introducing hydrogen under the action of a catalyst, and carrying out a reaction to obtain the product. According to the method, on the basis of the process of the BASF company, after triethylamine hydrochloride is formed by triethylamine serving as an acid-binding agent, triethylamine is released from the triethylamine hydrochloride by using proper metal, so that the triethylamine serving as the acid-binding agent can be recycled, and the triethylamine only plays a role of a bridge in a system; through continuous exchange and circulation of a small amount of triethylamine, the reaction is carried out until the reaction is complete.

PROCESS FOR PREPARING 2,2,4,4-TETRAMETHYL-1,3-CYCLOBUTANEDIOL

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Paragraph 0160-0173, (2019/10/08)

Disclosed is a method for preparing 2,2,4,4-tetramethyl-1,3-cyclobutanediol, which prepares (E) 2,2,4,4-tetramethyl-1,3-cyclobutanediol (CBDO) which is a final material by sequentially going through (A) methacrylic acid (MAA) as a raw material, and (B) isobutyric acid (IBA), (C) isobutyric anhydride (IBAN), and (D) 2,2,4,4-tetramethyl-1,3-cyclobutanedione (CBDK) as an intermediate. According to the present invention, the method for preparing 2,2,4,4-tetramethyl-1,3-cyclobutanediol which is economical and eco-friendly by optimizing preparation steps and maximizing the efficiency is provided.COPYRIGHT KIPO 2019

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

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Paragraph 0032, (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.

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