1785-64-4 Usage
Uses
Used in Electronic Products Industry:
Dimer,Parylene F is used as a conformal coating for electronic products for its ability to provide barrier layer protection for high temperature applications, protect devices from moisture, bodily fluids, corrosive gases, vapors, liquids, and other contamination, waterproof electronics up to IPX8 protection level, meet requirements for IPC, MIL specs and NASA standards, prevent corrosion of printed circuit boards and electronic components, act as a dielectric layer to protect electronics from shorts and arcing, and provide thin film encapsulation to protect electronics from vibration or shock.
Used in Tin Whisker Mitigation:
Dimer,Parylene F is used as a conformal coating to mitigate tin whisker issues, as it can prevent the formation and growth of tin whiskers on electronic components.
Physical properties of deposited Parylene F film include gas permeability, short term service temperature, continuous service temperature, coefficient of friction, Rockwell hardness, tensile strength, penetration power, dielectric strength, and USP Class VI Polymer compliance.
benefits
Parylene F film meets all requirements of MIL-I-46058C, IPC-CC-830B and NASA-STD-8739.1 as type XYUSP Class VI biocompatibilityUL-94 V-0 flammability ratingNo VOC's or solvents used in deposition processRoHS and REACH compliantVapor deposition has a high penetration power and is extremely conformalDeposition occurs in a vacuum chamber occurs at room temperature and does not exert any force during depositionNo curing cycleExcellent barrier and dielectric propertiesChemically and biologically inertExtremely thin and lightweight coatingNo outgassing, approved by NASA HydrophobicAble to sterilize with all common sterilization methods
storage
Store in a cool, dark place in the original unopened container when not in use. Do not place in view of UV light source including sunlight. Dimer is not known to degrade when stored out of direct sunlight and below 30°C. Recommend retesting after five years from manufacturer date.
Check Digit Verification of cas no
The CAS Registry Mumber 1785-64-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,8 and 5 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1785-64:
(6*1)+(5*7)+(4*8)+(3*5)+(2*6)+(1*4)=104
104 % 10 = 4
So 1785-64-4 is a valid CAS Registry Number.
1785-64-4Relevant academic research and scientific papers
Preparation method of parylene
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Paragraph 0067-0069; 0072-0073, (2021/04/03)
The invention discloses a preparation method of parylene. The method comprises the steps: carrying out a reaction on a compound 1A to obtain a compound 2A; and reacting the compound 2A with a compound2B to obtain a parylene crude product, and purifying the parylene crude product to obtain a parylene fine product. According to the method, the reagent with lower price is used as a starting raw material, the final product is obtained through two-step reaction, the reaction condition of each step is mild, the yield of the obtained parylene is high, and the cost can be greatly reduced.
Octafluorofluoro-cyclic di-p-xylyene and synthesis method thereof
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Paragraph 0049-0073, (2019/02/04)
The invention discloses a method for synthesizing octafluorofluoro-cyclic di-p-xylyene. The octafluorofluoro-cyclic di-p-xylyene is prepared from 2,3,5,6-tetrafluoro-p-xylylene dichloride, comprisingthe following steps: step 1: add Zinc powder, solvent, p
Method for using microchannel reactor to prepare paracyclophane monomeric compound
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Paragraph 0070; 0074-0077, (2017/08/23)
The invention discloses a method for using a microchannel reactor to prepare a paracyclophane monomeric compound. The method comprises the steps of preheating, intermediate synthesizing, product synthesizing, oil-water separating, purifying and the like. The paracyclophane monomeric compound is prepared in the continuous microchannel reactor. The method for using the microchannel reactor to prepare the paracyclophane monomeric compound has the advantages of being low in cost and small in energy consumption, having less three wastes, having continuous controllability, having no amplification effect and the like, and is capable of being subjected to simple amplification with equal ratio according to a demand of practical production.
