27327-67-9 Usage
Uses
Used in Adhesives and Coatings Industry:
1,4-Cyclohexanedicarbohydrazide is used as a crosslinking agent for enhancing the durability and performance of adhesives and coatings.
Used in Polymer Production:
1,4-Cyclohexanedicarbohydrazide serves as a crosslinking agent in the production of polymers, improving their structural integrity and thermal resistance.
Used as a Curing Agent for Epoxy Resins:
In the composite materials industry, 1,4-Cyclohexanedicarbohydrazide is utilized as a curing agent for epoxy resins, contributing to the formation of strong and heat-resistant materials.
Used as a Blowing Agent for Foams:
1,4-Cyclohexanedicarbohydrazide is employed as a blowing agent in the manufacturing of foams, helping to create lightweight and insulating materials.
Used as an Antimicrobial Additive:
In consumer products such as textiles and plastics, 1,4-Cyclohexanedicarbohydrazide is used for its antimicrobial properties, providing protection against microbial growth and ensuring cleanliness.
However, it is important to handle 1,4-Cyclohexanedicarbohydrazide with care, as exposure may cause irritation to the skin, eyes, and respiratory tract.
Check Digit Verification of cas no
The CAS Registry Mumber 27327-67-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,3,2 and 7 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 27327-67:
(7*2)+(6*7)+(5*3)+(4*2)+(3*7)+(2*6)+(1*7)=119
119 % 10 = 9
So 27327-67-9 is a valid CAS Registry Number.
InChI:InChI=1/C8H16N4O2/c9-11-7(13)5-1-2-6(4-3-5)8(14)12-10/h5-6H,1-4,9-10H2,(H,11,13)(H,12,14)
27327-67-9Relevant academic research and scientific papers
Ultralow-Molecular-Weight Stimuli-Responsive and Multifunctional Supramolecular Gels Based on Monomers and Trimers of Hydrazides
Wu, Dehua,Song, Jintong,Qu, Lang,Zhou, Weilan,Wang, Lei,Zhou, Xiangge,Xiang, Haifeng
supporting information, p. 3370 - 3378 (2020/10/02)
The simpler, the better. A series of simple, neutral and ultralow-molecular-weight (MW: 140–200) hydrazide-derived supramolecular gelators have been designed and synthesized in two straightforward steps. For non-conjugated cyclohexane-derived hydrazides, their monomers can self-assemble to form gels through intermolecular hydrogen bonds and dipole-dipole interactions. Significantly, conjugated phthalhydrazide can self-aggregate into planar and circular trimers through intermolecular hydrogen bonds and then self-assemble to form gels through intermolecular π–π stacking interactions. It is interesting that these simple gelators exhibit unusual properties, such as self-healing, multi-response fluorescence, and visual and selective recognition of chiral (R)/(S)-1,1′-binaphthalene-2,2′-diamine and S2? through much different times of gel re-formation and blue-green color change, respectively. These results underline the importance of supramolecular gels and extend the scope of supramolecular gelators.
