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1,6-Hexanediol dimethacrylate is a clear liquid chemical compound that is commonly utilized in the production of various materials and products due to its unique properties.

6606-59-3

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6606-59-3 Usage

Uses

Used in Automotive Industry:
1,6-Hexanediol dimethacrylate is used as a raw material for the preparation of sheet-shaped molding compounds. It is particularly valuable in the automotive field, where it contributes to the creation of durable and high-quality components for vehicles. 1,6-Hexanediol dimethacrylate's properties make it suitable for use in this industry, enhancing the performance and longevity of automotive parts.

Check Digit Verification of cas no

The CAS Registry Mumber 6606-59-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,6,0 and 6 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 6606-59:
(6*6)+(5*6)+(4*0)+(3*6)+(2*5)+(1*9)=103
103 % 10 = 3
So 6606-59-3 is a valid CAS Registry Number.
InChI:InChI=1/C14H22O4/c1-11(2)13(15)17-9-7-5-6-8-10-18-14(16)12(3)4/h1,3,5-10H2,2,4H3

6606-59-3 Well-known Company Product Price

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  • Aldrich

  • (411736)  1,6-Hexanedioldimethacrylate  contains 100 ppm hydroquinone as inhibitor, ≥90%

  • 6606-59-3

  • 411736-100ML

  • 976.95CNY

  • Detail

6606-59-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,6-Bis(methacryloyloxy)hexane

1.2 Other means of identification

Product number -
Other names 2-Propenoic acid, 2-methyl-, 1,6-hexanediyl ester

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Photosensitive chemicals
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:6606-59-3 SDS

6606-59-3Downstream Products

6606-59-3Relevant academic research and scientific papers

Preparation method of dihydric alcohol unsaturated carboxylate

-

Paragraph 0023, (2018/02/04)

The invention discloses a preparation method of dihydric alcohol unsaturated carboxylate. The method comprises the following steps: 1, adding thionyl chloride to dihydric alcohol in a dropwise manner, carrying out a reaction after dropwise addition is completed, and washing a material obtained after the reaction with water to obtain dihydric alcohol chloride; and 2, adding unsaturated carboxylic acid to the dihydric alcohol chloride obtained in step 1, adding an alkaline substance, adding a polymerization inhibitor, uniformly stirring above materials, heating the obtained mixture to 80-120DEG C, reacting the heated mixture for 1-24h, and centrifuging the obtained reaction product to remove generated chloride and unsaturated carboxylate in order to obtain dihydric alcohol unsaturated carboxylate. The method has the advantages of simple technology, environmental protection, no generation of wastewater, no use of flammable, combustible or carcinogenic organic solvents, no generation of waste gases, and realization of reduction of corrosion to a reaction device and prolongation of the service life of the device due to no use of strong acidic substances in the reactions.

Dental fillers including a phosphorus-containing surface treatment, and compositions and methods thereof

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Page/Page column 18, (2016/05/09)

The present application provides dental fillers, and methods of making and using dental fillers that include a treated surface that includes phosphorus and a divalent cation. Dental compositions including such dental fillers can be useful for delivering ions to the oral environment.

Polymerizable mesogen compound having improved photoreactive efficiency and polymerizable liquid crystal compositions containing the same

-

Paragraph 0129-0131, (2016/12/26)

The present invention relates to a polymerizable mesogen compound having improved photo-reaction efficiency by introducing an alpha-thiomethyl acrylate group as a photo-reactive group, and to a polymerizable liquid crystal composition containing the same. The polymerizable mesogen compound of the present invention has improved photo-reaction efficiency at a relatively low energy state by introducing an alpha-thiomethyl acrylate group as a photo-reactive group, retains excellent solubility in a host liquid crystal due to an asymmetric structure thereof, and improves stability of the pretilt angle after photo-crosslinking, and thus can be useful as a polymerizable liquid crystal composition, particularly, a polymerizable liquid crystal composition for a polymer stabilization alignment type liquid crystal display.

Hydroxy functional acrylate and methacrylate monomers prepared via lipase-catalyzed transacylation reactions

Popescu, Dragos,Hoogenboom, Richard,Keul, Helmut,Moeller, Martin

experimental part, p. 80 - 89 (2010/08/20)

Candida antarctica lipase B (CAL-B, Novozyme 435) catalyzes the transacylation of methyl acrylate and methyl methacrylate with diols and triols in 2-methyl-2-butanol at 50 °C. Under the experimental conditions, up to 70 mol% of the acyl donor methyl acrylate was converted. Methyl methacrylate is the less efficient acyl donor (up to 60 mol%) due to the higher sterical hindrance in the enzymatic transacylation. Under the reaction conditions high yields of the mono-acylated products are obtained, which contain minor amounts of bis(meth)acrylates. In addition it was observed that Novozyme 435 catalyzes regioselectively the acylation of the primary hydroxyl groups. In comparison with the chemical catalyzed route no selectivity was observed for unsubstituted diols. For substituted diols more mono-acylated product was formed in the lipase-catalyzed reaction than in the chemical catalyzed reaction.

DENTAL COMPOSITIONS WITH SURFACE-TREATED FILLER FOR SHELF STABILITY

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Page/Page column 28, (2008/06/13)

The invention features dental compositions containing a basic filler that has been surface-treated with a strong acid to increase the shelf life of the composition.

DENTAL COMPOSITIONS WITH A WATER SCAVENGER

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Page/Page column 27-28, (2008/06/13)

The present invention relates to polymerizable dental compositions that contain a water scavenger, such as a molecular sieve, to increase the shelf life of the composition.

DENTAL COMPOSITIONS WITH CALCIUM PHOSPHORUS RELEASING GLASS

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Page/Page column 30-31, (2008/06/13)

The present application provides dental compositions, and methods of making and using dental compositions that include a calcium and phosphorus releasing glass. Such dental compositions can be useful for delivering ions to the oral environment.

DENTAL FILLERS AND COMPOSITIONS INCLUDING PHOSPHATE SALTS

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Page/Page column 28-29, (2008/06/13)

The present application provides dental fillers, and methods of making and using dental fillers that include a treated surface that includes a phosphate salt. Dental compositions including such dental fillers can be useful for delivering ions to the oral environment. Dental compositions, and methods of using dental compositions that include a phosphate salt and a hardenable resin or a water-dispersible, polymeric film former are also provided.

SELF-ADHESIVE COMPOSITIONS INCLUDING A PLURALITY OF ACIDIC COMPOUNDS

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Page/Page column 27, (2008/06/13)

The present invention provides self-adhesive compositions that include a plurality of acidic compounds. The self-adhesive compositions are useful for applications including, for example, restoring dental structures and adhering orthodontic appliances to teeth.

DENTAL METHODS, COMPOSITIONS, AND KITS INCLUDING ACID-SENSITIVE DYES

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Page/Page column 17-18, (2008/06/13)

Methods and compositions including an aqueous liquid that includes an acid-sensitive dye are disclosed for use in dental and orthodontic procedures. The aqueous liquid can be useful for providing a visible color change to indicate contact with acidic materials including, for example, etching compositions, self-etching adhesives, and self-adhesive compositions.

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