10220-20-9 Usage
Description
1 1'-DITHIOBISPIPERIDINE 99, also known as DTBP, is a chemical compound that is widely recognized for its high reactivity and effectiveness in promoting crosslinking reactions. It is commonly used as a crosslinking agent in polymers and as a vulcanizing agent in rubber products, making it a valuable ingredient in various industrial applications. Due to its potential to cause irritation and toxicity if mishandled, it is important to handle and store this chemical with care.
Uses
Used in Polymer Industry:
1 1'-DITHIOBISPIPERIDINE 99 is used as a crosslinking agent for enhancing the mechanical properties, thermal stability, and durability of polymers. Its high reactivity ensures efficient crosslinking reactions, leading to improved performance of the final polymer products.
Used in Rubber Industry:
In the rubber industry, 1 1'-DITHIOBISPIPERIDINE 99 is used as a vulcanizing agent to improve the elasticity, strength, and resistance to wear and tear of rubber products. The vulcanization process facilitated by DTBP results in rubber products with enhanced durability and performance.
Used in Pharmaceutical Industry:
1 1'-DITHIOBISPIPERIDINE 99 is utilized in the production of pharmaceutical compounds, where its crosslinking properties contribute to the development of various drugs and medications. Its reactivity and effectiveness in promoting crosslinking reactions make it a valuable component in the synthesis of pharmaceutical products.
Used in Oilfield Chemicals:
As a stabilizer in oilfield chemicals, 1 1'-DITHIOBISPIPERIDINE 99 plays a crucial role in enhancing the stability and performance of drilling fluids and other oilfield applications. Its ability to promote crosslinking reactions contributes to the improved rheological properties and overall effectiveness of these chemicals in the oil and gas industry.
Check Digit Verification of cas no
The CAS Registry Mumber 10220-20-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,2,2 and 0 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 10220-20:
(7*1)+(6*0)+(5*2)+(4*2)+(3*0)+(2*2)+(1*0)=29
29 % 10 = 9
So 10220-20-9 is a valid CAS Registry Number.
10220-20-9Relevant articles and documents
Design, synthesis, and insecticidal activities of new N-benzoyl-N'-phenyl- N'-sulfenylureas
Sun, Ranfeng,Zhang, Yonglin,Chen, Li,Li, Yongqiang,Li, Qingshan,Song, Haibin,Huang, Runqiu,Bi, Fuchun,Wang, Qingmin
experimental part, p. 3661 - 3668 (2010/06/19)
Aseries of new N'-alkylaminothio,N'-arylaminothio (or dithio), and N',N'-thio (or dithio) derivatives ofN'-benzoyl-N'-phenylureas were designed and synthesized as insect-growth regulators with sulfur dichloride or disulfur dichloride as the original reactant. The new compounds were identified by 1H nuclear magnetic resonancee (NMR) spectroscopy, elemental analysis [or high-resolution mass spectrometry (HRMS)], and single-crystal X-ray diffraction analysis. The X-ray results demonstrated that there exist N-S-N or N-S-S-N bonds in these new compounds. In comparison to the parent N-benzoyl-N'-phenylureas, these derivatives displayed better solubility. The insecticidal activities of the target compounds were evaluated. The results of bioassays showed that compounds 1-24 retained the larvicidal activities of the corresponding benzoylphenylureas (BPUs) and some compounds exhibited better larvicidal activities against oriental armyworm and mosquitoes than the parent BPUs. The larvicidal activities of the selected target compounds 1 and 24 against diamondback moth were better than that of the corresponding parent compounds E and triflumuron.
Method of treating a disease condition caused or exacerbated by an HPV
-
Page/Page column 17-18, (2008/06/13)
The invention provides agents and compounds (see (I) and (II)) for use in the treatment or prophylaxis of disease conditions caused or exacerbated by mammalian papillomaviruses, such as human papillomaviruses, as well as methods for the treatment or prevention thereof. In said formulae, R1–R4 and n are as defined herein.
A new method for the synthesis of N,N′-thiobisamines
Dudin
, p. 1796 - 1797 (2007/10/03)
Reaction of secondary amines (morpholine and piperidine) with sulfur and iodine afforded N,N′-thiobisamines in good yields.
