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1-HEXYL-3-PHENYL-2-THIOUREA, also known as HTU, is an organosulfur compound with the molecular formula C13H20N2S. It is widely recognized for its role as a rubber accelerator and anti-scorching agent in the synthesis of rubber, as well as for its utility as an intermediate in the production of pharmaceuticals and agrochemicals. HTU's industrial applications are significant due to its ability to expedite the vulcanization process in rubber manufacturing. However, it is crucial to handle this chemical with care, given its potential hazards if not properly controlled and managed.

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  • 15153-13-6 Structure
  • Basic information

    1. Product Name: 1-HEXYL-3-PHENYL-2-THIOUREA
    2. Synonyms: 1-HEXYL-3-PHENYL-2-THIOUREA;1-Hexyl-3-phenylthiourea;N-Hexyl-N'-phenylthiourea
    3. CAS NO:15153-13-6
    4. Molecular Formula: C13H20N2S
    5. Molecular Weight: 236.38
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 15153-13-6.mol
  • Chemical Properties

    1. Melting Point: 104°C
    2. Boiling Point: 331.2 °C at 760 mmHg
    3. Flash Point: 154.1 °C
    4. Appearance: /
    5. Density: 1.066 g/cm3
    6. Vapor Pressure: 0.000158mmHg at 25°C
    7. Refractive Index: 1.587
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. PKA: 12.75±0.70(Predicted)
    11. CAS DataBase Reference: 1-HEXYL-3-PHENYL-2-THIOUREA(CAS DataBase Reference)
    12. NIST Chemistry Reference: 1-HEXYL-3-PHENYL-2-THIOUREA(15153-13-6)
    13. EPA Substance Registry System: 1-HEXYL-3-PHENYL-2-THIOUREA(15153-13-6)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: IRRITANT
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 15153-13-6(Hazardous Substances Data)

15153-13-6 Usage

Uses

Used in Rubber Industry:
1-HEXYL-3-PHENYL-2-THIOUREA is used as a rubber accelerator for its ability to speed up the vulcanization process, which is essential for the production of rubber goods. This function enhances the efficiency and quality of rubber manufacturing.
1-HEXYL-3-PHENYL-2-THIOUREA is also used as an anti-scorching agent to prevent premature vulcanization, which can damage rubber products and equipment during the manufacturing process.
Used in Pharmaceutical Industry:
HTU serves as an intermediate in the production of various pharmaceuticals, contributing to the synthesis of drugs that address a range of health conditions.
Used in Agrochemical Industry:
In the agrochemical sector, 1-HEXYL-3-PHENYL-2-THIOUREA is utilized as an intermediate in the synthesis of agrochemicals, playing a role in the development of products that protect and enhance crop yields and quality.

Check Digit Verification of cas no

The CAS Registry Mumber 15153-13-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,1,5 and 3 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 15153-13:
(7*1)+(6*5)+(5*1)+(4*5)+(3*3)+(2*1)+(1*3)=76
76 % 10 = 6
So 15153-13-6 is a valid CAS Registry Number.
InChI:InChI=1/C13H20N2S/c1-2-3-4-8-11-14-13(16)15-12-9-6-5-7-10-12/h5-7,9-10H,2-4,8,11H2,1H3,(H2,14,15,16)

15153-13-6SDS

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-Hexyl-3-phenyl-2-thiourea

1.2 Other means of identification

Product number -
Other names 1-hexyl-3-phenylthiourea

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:15153-13-6 SDS

15153-13-6Relevant articles and documents

N-Terminal guanidine derivatives of teicoplanin antibiotics strongly active against glycopeptide resistant Enterococcus faecium

Sz?cs, Zsolt,Bereczki, Ilona,R?th, Erzsébet,Milánkovits, Márton,Ostorházi, Eszter,Batta, Gyula,Nagy, Lajos,Dombrádi, Zsuzsanna,Borbás, Anikó,Herczegh, Pál

, p. 603 - 614 (2020/05/19)

Antibiotic resistance is one of the major challenges in healthcare of our time. To meet this challenge, we designed and prepared guanidine and lipophilic guanidine derivatives of the glycopeptide antibiotic teicoplanin to armed them with activity against

Convenient synthesis of unsymmetrical N,N′-disubstituted thioureas in water

Li, Zhengyi,Chen, Yuan,Yin, Yue,Wang, Zhiming,Sun, Xiaoqiang

, p. 670 - 673 (2016/11/18)

A simple and convenient two-step method has been developed and used to synthesise 25 (4 of which are novel) unsymmetrical N,N′-disubstituted thioureas in water. Alkylamines or variously substituted arylamines reacted smoothly with phenyl chlorothionoformate at room temperature to form thiocarbamates, which were then reacted with another alkyl- or arylamine in water at reflux to afford the unsymmetrical N,N′-disubstituted thioureas in good to excellent yields. Mild conditions, simple work-up, high yields as well as using water as solvent are the major advantages of the method.

METHODS OF PRODUCING METAL SUFLIDES, METAL SELENIDES, AND METAL SULFIDES/SELENIDES HAVING CONTROLLED ARCHITECTURES USING KINETIC CONTROL

-

Paragraph 0204; 0205; 0214, (2017/05/28)

The present invention is directed to methods of preparing metal sulfide, metal selenide, or metal sulfide/selenide nanoparticles and the products derived therefrom. In various embodiments, the nanoparticles are derived from the reaction between precursor metal salts and certain sulfur- and/or selenium-containing precursors each independently having a structure of Formula (I), (II), or (III), or an isomer, salt, or tautomer thereof, where Q1,Q2,Q3,R1,R2,R3,R5, and X are defined within the specification.

A Tunable library of substituted thiourea precursors to metal sulfide nanocrystals

Hendricks, Mark P.,Campos, Michael P.,Cleveland, Gregory T.,Plante, Ilan Jen-La,Owen, Jonathan S.

, p. 1226 - 1230 (2015/06/22)

Controlling the size of colloidal nanocrystals is essential to optimizing their performance in optoelectronic devices, catalysis, and imaging applications. Traditional synthetic methods control size by terminating the growth, an approach that limits the reaction yield and causes batch-to-batch variability. Herein we report a library of thioureas whose substitution pattern tunes their conversion reactivity over more than five orders of magnitude and demonstrate that faster thiourea conversion kinetics increases the extent of crystal nucleation. Tunable kinetics thereby allows the nanocrystal concentration to be adjusted and a desired crystal size to be prepared at full conversion. Controlled precursor reactivity and quantitative conversion improve the batch-tobatch consistency of the final nanocrystal size at industrially relevant reaction scales.

Thiourea isosteres as anion receptors and transmembrane transporters

Wenzel, Marco,Light, Mark E.,Davis, Anthony P.,Gale, Philip A.

supporting information; experimental part, p. 7641 - 7643 (2011/09/15)

Compounds containing cyanoguanidine and 3-amino-1,2,4-benzothiadiazine-1,1- dioxide have been studied as anion receptors and transporters. Significant affinity for oxo-anions was observed in organic solution and the receptors were found to function as tra

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