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N-Phenyl-N'-(3-phenylpropyl)thiourea, a thiourea derivative with the molecular formula C16H18N2S, is a white crystalline solid that is relatively stable under normal conditions. It is primarily used as a rubber accelerator in the production of tires and other rubber products, as well as a catalyst in the synthesis of organic compounds and a stabilizer in the production of plastics. However, due to its irritant and toxic properties, it should be handled with care and proper safety precautions should be followed to avoid any potential health hazards.

15093-43-3

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15093-43-3 Usage

Uses

Used in Rubber Industry:
N-Phenyl-N'-(3-phenylpropyl)thiourea is used as a rubber accelerator for enhancing the vulcanization process in the production of tires and other rubber products. It helps to improve the strength, elasticity, and durability of rubber products.
Used in Chemical Synthesis:
N-Phenyl-N'-(3-phenylpropyl)thiourea is used as a catalyst in the synthesis of various organic compounds. Its unique chemical properties enable it to facilitate specific reactions, leading to the formation of desired products.
Used in Plastics Industry:
N-Phenyl-N'-(3-phenylpropyl)thiourea is used as a stabilizer in the production of plastics. It helps to prevent the degradation of plastic materials, thereby improving their longevity and performance.

Check Digit Verification of cas no

The CAS Registry Mumber 15093-43-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,0,9 and 3 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 15093-43:
(7*1)+(6*5)+(5*0)+(4*9)+(3*3)+(2*4)+(1*3)=93
93 % 10 = 3
So 15093-43-3 is a valid CAS Registry Number.
InChI:InChI=1/C16H18N2S/c19-16(18-15-11-5-2-6-12-15)17-13-7-10-14-8-3-1-4-9-14/h1-6,8-9,11-12H,7,10,13H2,(H2,17,18,19)

15093-43-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-phenyl-3-(3-phenylpropyl)thiourea

1.2 Other means of identification

Product number -
Other names HMS2964M10

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
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:15093-43-3 SDS

15093-43-3Downstream Products

15093-43-3Relevant academic research and scientific papers

Structural requirement of phenylthiourea analogs for their inhibitory activity of melanogenesis and tyrosinase

Thanigaimalai, Pillaiyar,Lee, Ki-Cheul,Sharma, Vinay K.,Joo, Cheonik,Cho, Won-Jea,Roh, Eunmiri,Kim, Youngsoo,Jung, Sang-Hun

experimental part, p. 6824 - 6828 (2011/12/22)

Effect of a series of 1-phenylthioureas 1a-k and 1,3-disubstituted thioureas 2a-k were evaluated against melanin formation in melanoma B16 cell line and mushroom tyrosinase. Inhibitory activity of tyrosinase of 1-phenylthioureas 1a-k is parallel to their melanogenic inhibition. Thus, the melanogenic inhibition in melanoma B16 cells of 1-phenylthioureas could be the result of inhibition of tyrosinase. However, 1,3-diaryl or 1-phenyl-3- alkylthioureas, 2a-k, appears as melanogenic inhibitor without inhibition of tyrosinase. The molecular docking study of 1e and 2b to binding pocket of tyrosinase provided convincing explanation regarding the necessity of direct connection of planar phenyl to thiourea unit without N′-substitution of phenylthioureas 1 as tyrosinase inhibitor and 2 as non-tyrosinase inhibitor.

ULTRAMINE: A high-capacity polyethylene-imine-based polymer and its application as a scavenger resin

Roice, Michael,Christensen, Soren F.,Meldal, Morten

, p. 4407 - 4415 (2007/10/03)

The synthesis of a novel high-loading polyethylene-imine resin (ULTRAMINE) is described, and its application as a scavenger resin in various acylation reactions is demonstrated. The inverse suspension polymerization technique was used for the synthesis of well-defined spherical polymer beads. Polymer beads with different cross-linking densities were synthesized according to the degree of acryloylation of the polyethylene-imine polymer. The resin was characterized by various spectroscopic techniques. The size, shape, and morphological features of the resin were demonstrated by microscopy. The resin showed excellent swelling properties in both polar and nonpolar solvents. The chemical stability of the resin in various reagents and solvents was investigated and monitored by IR spectroscopy. The mechanical stability of the beads was determined by a single-bead compressive experiment. The ULTRAMINE beads can be used as an excellent scavenger for excess acylating reagent, as demonstrated for a variety of reactions. UL-TRAMINE-red resin was derived from ULTRAMINE through exhaustive reduction of the amide carbonyl groups to yield an all-amine resin.

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