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1076-97-7

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1076-97-7 Usage

Chemical Properties

white fine crystalline powder

Uses

1,4-Cyclohexanedicarboxylic acid may be used in the synthesis of:polyesterspolyamidespoly(butylene adipate-co-butylene 1,4-cyclohexanedicarboxylate) copolyestervarious polyester polyols

General Description

1,4-Cyclohexanedicarboxylic acid (1,4-CHDA) has cyclohexane based structure. CHDA has better weatherability, higher impact strength, and faster stress relaxation. CHDA exhibits three isomeric forms:axial, axial (a,a) trans-isomerequatorial, equatorial (e,e) trans-isomer a,e cis-isomer

Flammability and Explosibility

Nonflammable

Check Digit Verification of cas no

The CAS Registry Mumber 1076-97-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,7 and 6 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1076-97:
(6*1)+(5*0)+(4*7)+(3*6)+(2*9)+(1*7)=77
77 % 10 = 7
So 1076-97-7 is a valid CAS Registry Number.
InChI:InChI=1/C10H16O2/c1-7(11)9-3-5-10(6-4-9)8(2)12/h9-10H,3-6H2,1-2H3

1076-97-7 Well-known Company Product Price

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  • Alfa Aesar

  • (B23125)  1,4-Cyclohexanedicarboxylic acid, cis + trans, 98%   

  • 1076-97-7

  • 100g

  • 254.0CNY

  • Detail
  • Alfa Aesar

  • (B23125)  1,4-Cyclohexanedicarboxylic acid, cis + trans, 98%   

  • 1076-97-7

  • 500g

  • 741.0CNY

  • Detail

1076-97-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,4-Cyclohexanedicarboxylic acid

1.2 Other means of identification

Product number -
Other names 1,4-trans-cyclohexyldicarboxylic acid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Intermediates,Paint additives and coating additives not described by other categories
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:1076-97-7 SDS

1076-97-7Related news

Isomer transformation and photoluminescence in novel coordination polymers constructed from 1,4-Cyclohexanedicarboxylic acid (cas 1076-97-7) and imidazole08/06/2019

Three novel coordination polymers [M(chdc)(imi)]n (chdc=1,4-cyclohexanedicarboxylic dianion, imi=imidazole, M=Ni 1, Co 2 and Zn 3) have been synthesized by solvothermal technique and characterized by elemental analysis, IR and single-crystal X-ray diffraction. The trans-chdc have been partially ...detailed

The assembly of two isomorphous coordination compounds based on 1,4-Cyclohexanedicarboxylic acid (cas 1076-97-7) and 2,4-diamino-6-phenyl-1,3,5-triazine08/02/2019

The compounds [Co(e,a-cis-1,4-chdc)(phdat)]n (1) and [Cd(e,a-cis-1,4-chdc)(phdat)]n (2) have been synthesized under hydrothermal method by using 1,4-cyclohexanedicarboxylic acid (1,4-H2chdc), 2,4-diamino-6-phenyl-1,3,5-triazine (phdat) as well as CoCl2·6H2O, CdCl2·2.5H2O respectively and chara...detailed

1076-97-7Relevant articles and documents

Synthesis of phthalate-free plasticizers by hydrogenation in water using RhNi bimetallic catalyst on aluminated SBA-15

Phan-Vu, Duc-Ha,Tan, Chung-Sung

, p. 18178 - 18188 (2017)

In this study, rhodium-nickel bimetallic nanoparticles loaded on aluminated silica (RhNi/Al-SBA-15) were used as catalysts for the hydrogenation of phthalate in water to produce environmentally acceptable non-phthalate plasticizers. Chemical fluid deposition (CFD) was used to dope metals onto the aluminated silica support, which helped to create a uniform structure of RhNi on Al-SBA-15. The introduction of Ni helped to reduce the use of expensive Rh and increase the number of metal active sites by reducing the bimetallic nanoparticle size. Aluminated SBA-15 not only acted as the support for the RhNi bimetallic catalyst but also enhanced the reaction efficiency by introducing Br?nsted and Lewis acid sites and the absorption of phthalates on the catalyst in water. The physicochemical properties of prepared catalysts were characterized by N2 adsorption-desorption isotherm, X-ray diffraction (XRD), in situ diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS), Scanning electron microscopy (SEM), and Transmission electron microscopy (TEM). The catalytic performance of the synthesized catalysts was evaluated with the hydrogenation of dimethyl phthalate (DMP). Despite the low solubility of DMP in water, the hydrogenation using Rh0.5Ni1.5/Al-SBA-15 was carried out with an 84.4% reaction yield (cis-?:?trans- = 97.5?:?2.5) at 80 °C using 1000 psi of H2 after 2 h.

Catalyst for aqueous phase catalytic hydrogenation of phthalic acids and ester derivatives thereof and preparation method and application thereof

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Paragraph 0046-0051; 0055-0056, (2020/07/13)

The invention discloses a catalyst for aqueous phase catalytic hydrogenation of phthalic acids and ester derivatives thereof, a preparation method and application thereof. The catalyst adopts an acidic composite carrier of aluminum-doped ordered mesoporous silica, and combines specific Si/Al, ordered mesoporous size and active component loading capacity to realize catalytic hydrogenation of phthalic acids and ester derivatives thereof in the water phase to prepare corresponding cyclohexanedicarboxylic acids and derivatives thereof. The catalyst is low in raw material cost, simple in preparation process and lower in noble metal loading capacity, wherein the catalytic reaction temperature is 40-100 DEG C, the hydrogen pressure is 3-6MPa, the reaction time is 0.2-3h, the conditions are mild,the solvent is pollution-free and the catalytic efficiency is high.

METHOD FOR PRODUCING 1,4-DICYANOCYCLOHEXANE, 1,4-BIS(AMINOMETHYL)CYCLOHEXANE AND 1,4-CYCLOHEXANEDICARBOXYLIC ACID

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, (2019/08/02)

A method for producing 1,4-dicyanocyclohexane, having a step of obtaining 1,4-dicyanocyclohexane by subjecting a heated concentrate of an aqueous ammonia solution of 1,4-cyclohexanedicarboxylic acid to a cyanation reaction.

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