88790-52-7 Usage
Common uses
Plasticizer in the production of polymers and resins
Flexible PVC products such as toys, vinyl flooring, and wire and cable insulation
Benefits
Improves flexibility of plastic materials
Enhances durability of plastic materials
Increases thermal stability of plastic materials
Health and environmental concerns
Linked to reproductive and developmental toxicity in animal studies
Proper handling and disposal are important to minimize potential negative effects
Chemical structure
Contains a propanediol backbone with a 2-hexyl group and two 4-methylbenzenesulfonate groups
Molecular weight
Approximately 414.59 g/mol
Physical state
Likely a liquid or viscous substance at room temperature
Solubility
Soluble in organic solvents, such as ethanol and acetone
Stability
Stable under normal temperature and pressure conditions, but may decompose upon exposure to heat, flame, or strong oxidizing agents
Regulatory status
May be subject to regulations and restrictions depending on the jurisdiction and intended use
Safety precautions
Use personal protective equipment (PPE) when handling
Store in a cool, dry, and well-ventilated area, away from incompatible substances
Dispose of according to local, national, and international regulations for hazardous materials
Check Digit Verification of cas no
The CAS Registry Mumber 88790-52-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,7,9 and 0 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 88790-52:
(7*8)+(6*8)+(5*7)+(4*9)+(3*0)+(2*5)+(1*2)=187
187 % 10 = 7
So 88790-52-7 is a valid CAS Registry Number.
88790-52-7Relevant articles and documents
Synthesis and Liquid Crystal Properties of Dimethylene Linked Compounds Incorporating the Cyclobutane or Spiroheptane Rings
Chan, L. K. M.,Gemmell, P. A.,Gray, G. W.,Lacey, D.,Toyne, K. J.
, p. 229 - 246 (2007/10/02)
The preparation of sixteen dimethylene linked compounds is described heptane ring>, and a comparison is made between the transition temperatures of these compounds and those of the corresponding esters.This comparison once again highlights the fact that the cyclobutane ring should be regarded, in terms of its ability to promote nematic thermal stability, as a "chain stiffener rather than as a ring system.A comparison is also made of the nematic thermal stabilities of the trans-cyclobutane and the spiroheptane systems and of the trans-cyclohexane and the spiroundecane systems.
LONG-ACTING CONTRACEPTIVE AGENTS: CYCLOPROPYL AND CYCLOBUTYL ESTERS OF NORETHISTERONE
Shafiee, A.,Vossoghi, M.,Savabi, F.,Vlahov, R.,Tarpanov, V.,et al.
, p. 291 - 308 (2007/10/02)
Several esters of norethisterone (17α-ethynyl-17β-hydroxyestr-4-en-3-one) with carboxylic acids containing a cyclopropyl or cyclobutyl ring have been synthesized and the stereochemistries of the side-chains determined.
