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Triapenthenol, also known as trimethylolpropane, is a versatile chemical compound belonging to the class of alcohols. It is characterized by its three hydroxyl groups, which make it highly reactive and a valuable intermediate in the production of polyester resins. Triapenthenol is used as a building block for creating coatings, adhesives, and sealants in various industrial applications, and also serves as a crosslinking agent in the production of polyurethane and epoxy resins, contributing to the manufacturing of high-performance materials. Its non-toxic nature and low acute toxicity make it a safe choice for use in a wide range of industrial and consumer products.

76608-88-3

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76608-88-3 Usage

Uses

Used in Coatings Industry:
Triapenthenol is used as a building block for creating coatings, providing enhanced properties such as adhesion, durability, and resistance to various environmental factors.
Used in Adhesives Industry:
In the adhesives industry, Triapenthenol is utilized as a component in the formulation of high-performance adhesives, offering improved bonding strength and resistance to different substrates.
Used in Sealants Industry:
Triapenthenol is employed as a key ingredient in the production of sealants, contributing to their flexibility, sealing capabilities, and resistance to various conditions.
Used in Polyester Resin Production:
As an important intermediate, Triapenthenol plays a crucial role in the synthesis of polyester resins, which are widely used in the manufacturing of composite materials, laminates, and other applications.
Used in Polyurethane and Epoxy Resin Production:
Triapenthenol serves as a crosslinking agent in the production of polyurethane and epoxy resins, enhancing the mechanical properties, chemical resistance, and thermal stability of the final products.
Used in High-Performance Material Manufacturing:
Due to its versatility and reactivity, Triapenthenol is an essential component in the development of high-performance materials, such as advanced composites, coatings, and adhesives, that exhibit superior properties for various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 76608-88-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,6,0 and 8 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 76608-88:
(7*7)+(6*6)+(5*6)+(4*0)+(3*8)+(2*8)+(1*8)=163
163 % 10 = 3
So 76608-88-3 is a valid CAS Registry Number.

76608-88-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name triapenthenol

1.2 Other means of identification

Product number -
Other names (E)-1-cyclohexyl-4,4-dimethyl-2-(1,2,4-triazol-1-yl)pent-1-en-3-ol

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:76608-88-3 SDS

76608-88-3Relevant articles and documents

Direct enantioseparation of nitrogen-heterocyclic pesticides on cellulose-based chiral column by high-performance liquid chromatography

Chai, Tingting,Yang, Wenwen,Qiu, Jing,Hou, Shicong

, p. 32 - 38 (2015/03/13)

The enantiomeric separation of eight pesticides including bitertanol (1), diclobutrazol (2), fenbuconazole (3), triticonazole (4), imazalil (5), triapenthenol (6), ancymidol (7), and carfentrazone-ethyl (8) was achieved, using normal-phase high-performanc

Process for producing optically active alcohol

-

, (2008/06/13)

The process for producing an optically active alcohol of the present invention comprises allowing (A) an optically active amino alcohol represented by the general formula (I) STR1 (R1 is an aryl group, R2 is a lower alkyl group, Rsu

Use of diphenyl ether derivatives for the desiccation and abscission of plant organs

-

, (2008/06/13)

The use of diphenyl ether derivatives of the general formula I STR1 where A is a radical STR2 where R1 is hydrogen, an alkali metal or alkaline earth metal ion, substituted or unsubstituted ammonium, alkyl of from 1 to 4 carbon atoms or alkoxycarbonylalkyl of a total of 1 to 6 carbon atoms and R2 is alkyl of from 1 to 4 carbon atoms, for the desiccation and abscission of plant organs.

Method for producing an optically active azolyl-α β-unsaturated alcohol

-

, (2008/06/13)

The present invention relates to a method for producing optically active alcohol derivatives, which are useful as fungicides, herbicides or plant growth regulators, represented by the formula, STR1 by carrying out the asymmetric reduction of a ketone compound represented by the formula, STR2 with a boron hydride-reducing agent modified with an optically active amino alcohol represented by the formula, STR3 and also relates to the boron hydride type compound obtained by reacting the above optically active amino alcohol with a boron hydride compound and its production method.

Process for the preparation of the (-)-antipode of (E)-1-cyclohexyl-4, 4-dimethyl-3-hydroxy-2-(1,2,4-triazol-1-yl)-pent-1-ene

-

, (2008/06/13)

A process for the preparation of the (-)-antipode of (E)-1-cyclohexyl-4,4-dimethyl-3-hydroxy-2-(1,2,4-triazol-1-yl)-pent-1-ene of the formula STR1 which comprises reacting the (E)-isomer of 1-cyclohexyl-4,4-dimethyl-2-(1,2,4-triazol-1-yl)-pent-1-en-3-one of the formula STR2 (a) with boron hydride in the presence of an optically active proline derivative of the formula STR3 in which, R1 is alkyl, phenyl or benzyl, or (b) with a complex borohydride in the presence of an acid addition salt of the optically active proline derivative, in the presence of a diluent at a temperature between about -70° C. and +60° C. The proline derivatives are also new and are produced from S-proline esters. The end product is a known plant growth regulant.

Asymmetrically modified boron hydride type compound, a production method thereof, and a method for producing an optically active alcohol derivative by the use thereof

-

, (2008/06/13)

The present invention relates to an asymmetrically modified borohydride type compound obtained by reacting an optically active amino alcohol represented by the formula, STR1 or its salt with an acid with a borohydride compound; its production method; and a method for producing an optically active alcohol derivative useful as fungicides, herbicides or plant growth regulators and represented by the formula, STR2 which comprises asymmetrically reducing a ketone compound represented by the formula, STR3 with the asymmetrically modified borohydride type compound.

(-)-Antipode of (E)-1-cyclohexyl-4,4-dimethyl-3-hydroxy-2-(1,2,4-triazol-1-yl)-pent-1-ene

-

, (2008/06/13)

(-)-Antipode of (E)-1-cyclohexyl-4,4-dimethyl-3-hydroxy-2-(1,2,4-triazol-1-yl)-pent-1-ene of the formula STR1 a plant growth regulant containing the same and a process for regulating the growth of plants are disclosed. Also disclosed is a method for making such antipode.

Synergistic compositions for inhibiting plant growth

-

, (2008/06/13)

A plant growth-inhibiting composition comprising STR1 wherein the various radicals are as defined.

1-Vinyltriazole compounds and plant growth and fungicidal compositions

-

, (2008/06/13)

1-Vinyltriazole compounds of the formula STR1 wherein R1 is alkyl, substituted alkyl, cycloalkyl, aryl or substituted aryl; R2 is alkyl; R3 is alkyl, cycloalkyl, cycloalkenyl, substituted cycloalkenyl, alkenyl, aryl or substituted aryl; or R2 and R3, together with the carbon to which they are bonded, represent cycloalkenyl, substituted cycloalkenyl, cycloalkyl or substituted cycloalkyl; X is the group STR2 or, alternatively, X may represent a keto group provided that when X is a keto group, R1 is alkyl, substituted alkyl, cycloalkyl, or substituted cycloalkyl; R4 is hydrogen, alkyl, aralkyl, substituted aralkyl, acyl, carbamoyl or substituted carbamoyl; R5 is hydrogen, alkyl, aralkyl or substituted aralkyl; and acid addition salts and metal salt complexes thereof; are outstandingly effective plant growth regulants and as fungicides.

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