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  • 143-10-2 Structure
  • Basic information

    1. Product Name: 1-Decanethiol
    2. Synonyms: Decyl mercaptan, Mercaptan C10;1-Decanethiol,98%;Decane-1-thiol 96%;Decyl mercaptan, 1-Mercaptodecane;N-decatyl mercaptan;decane-1-thiol;decanethiol;Decanethiol-(1)
    3. CAS NO:143-10-2
    4. Molecular Formula: C10H22S
    5. Molecular Weight: 174.35
    6. EINECS: 205-584-2
    7. Product Categories: Building Blocks;Chemical Synthesis;Organic Building Blocks;Sulfur Compounds;Thiols/Mercaptans
    8. Mol File: 143-10-2.mol
    9. Article Data: 24
  • Chemical Properties

    1. Melting Point: −26 °C(lit.)
    2. Boiling Point: 114 °C13 mm Hg(lit.)
    3. Flash Point: 209 °F
    4. Appearance: /
    5. Density: 0.841 g/mL at 25 °C(lit.)
    6. Refractive Index: n20/D 1.458(lit.)
    7. Storage Temp.: 2-8°C
    8. Solubility: N/A
    9. PKA: 10.50±0.10(Predicted)
    10. Water Solubility: Insoluble in water.
    11. Sensitive: Air Sensitive/Stench
    12. BRN: 1735223
    13. CAS DataBase Reference: 1-Decanethiol(CAS DataBase Reference)
    14. NIST Chemistry Reference: 1-Decanethiol(143-10-2)
    15. EPA Substance Registry System: 1-Decanethiol(143-10-2)
  • Safety Data

    1. Hazard Codes: Xi
    2. Statements: 36/37/38
    3. Safety Statements: 26-36
    4. RIDADR: UN 3334
    5. WGK Germany: 3
    6. RTECS:
    7. F: 13
    8. TSCA: Yes
    9. HazardClass: N/A
    10. PackingGroup: N/A
    11. Hazardous Substances Data: 143-10-2(Hazardous Substances Data)

143-10-2 Usage

Description

1-Decanethiol is an alkanethiol that forms a self-assembled monolayer (SAM) and is characterized by its liquid chemical properties. It can be coated as a protective coating on a variety of substrates, making it a versatile compound with applications in various industries.

Uses

Used in Electronics Industry:
1-Decanethiol is used as a charge injection enhancer for improving the performance of field-effect transistors (FETs). It is applied by creating a monolayer on gold source-drain electrode surfaces, which aids in the efficient transfer of charge between the device and the electrodes.
Used in Nanotechnology and Surface Science:
1-Decanethiol is used as a component in the study of self-assembled monolayers (SAMs). These monolayers are crucial in nanotechnology and surface science for their ability to create well-ordered structures on surfaces, which can be utilized in various applications such as sensors, catalysts, and molecular electronics.
Used in Surface Protection and Coating Industry:
1-Decanethiol is used as a protective coating on a variety of substrates due to its ability to form a self-assembled monolayer. This application is beneficial in industries where surface protection and resistance to environmental factors are essential, such as aerospace, automotive, and industrial manufacturing.

Reactivity Profile

1-Decanethiol is incompatible with oxidizing agents, strong acids and bases, alkali metals, and nitric acid. May react with water, steam or acids to produce toxic and flammable vapors. Reacts violently with strong oxidizing agents such as calcium hypochlorite(Ca(OCl)2) forming toxic fumes of SOx. Will react with hydrides to form flammable H2 gas. May react with halogenated hydrocarbons to yield hydrogen halides. Reacts exothermically with aldehydes. May mit highly toxic fumes of SO when heated to decomposition.

Check Digit Verification of cas no

The CAS Registry Mumber 143-10-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,4 and 3 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 143-10:
(5*1)+(4*4)+(3*3)+(2*1)+(1*0)=32
32 % 10 = 2
So 143-10-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H22S/c1-2-3-4-5-6-7-8-9-10-11/h11H,2-10H2,1H3

143-10-2 Well-known Company Product Price

  • Brand
  • (Code)Product description
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  • Alfa Aesar

  • (A15913)  1-Decanethiol, 96%   

  • 143-10-2

  • 25ml

  • 200.0CNY

  • Detail
  • Alfa Aesar

  • (A15913)  1-Decanethiol, 96%   

  • 143-10-2

  • 100ml

  • 648.0CNY

  • Detail
  • Alfa Aesar

  • (A15913)  1-Decanethiol, 96%   

  • 143-10-2

  • 500ml

  • 2992.0CNY

  • Detail
  • Aldrich

  • (D1602)  1-Decanethiol  96%

  • 143-10-2

  • D1602-50ML

  • 678.60CNY

  • Detail
  • Aldrich

  • (705233)  1-Decanethiol  99%

  • 143-10-2

  • 705233-1G

  • 2,095.47CNY

  • Detail

143-10-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-Decanethiol

1.2 Other means of identification

Product number -
Other names n-decyl mercaptan

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:143-10-2 SDS

143-10-2Related news

In situ STM imaging of individual molecules in two-component self-assembled monolayers of 3-mercaptopropionic acid and 1-Decanethiol (cas 143-10-2) on Au(111)09/30/2019

Two-component self-assembled monolayers composed of 3-mercaptopropionic acid (MPA) and 1-decanethiol (CH 3 (HC 2 ) 9 SH:C 1 0 SH) on Au(111) were investigated with in situ scanning tunneling microscopy (STM) and cyclic voltammetry, where the monolayers I and I...detailed

A study of 1-Decanethiol (cas 143-10-2) self-assembly on gold electrodes by computer simulation09/29/2019

This work is a preliminary study towards the understanding of the adsorption and self-assembly mechanisms of alkylthiols on gold electrodes. Canonical Monte Carlo simulations were performed at 298 K. The simulated model consisted of diluted solutions of 1-decanethiol in ethanol inside two gold e...detailed

143-10-2Relevant articles and documents

ACTIVATION OF NITROSO GROUP WITH THIOLS. A NEW TRANSFORMATION OF PRIMARY AMINES TO ORGANIC SULFIDES OR THIOLS

Ueno, Yoshio,Tanaka, Chie,Okawara, Makoto

, p. 2675 - 2678 (1984)

Aliphatic primary amines reacted with 2-mercaptobenzothiazole in the presence of t-butylnitrite at room temperature to give condensation products, 2-(alkylthio)benzothiazole.

Amphiphilic dendrimer, synthesis method thereof, and application of amphiphilic dendrimer as drug delivery system

-

Paragraph 0096-0097; 0108-0110, (2021/08/07)

The invention relates to a microenvironment response type amphiphilic dendrimer, a synthesis method thereof, and application of the microenvironment response type amphiphilic dendrimer as a drug delivery system. The microenvironment response type amphiphilic dendrimer is a compound with a structure as shown in a formula (I), a formula (II) or a formula (III) or pharmaceutically acceptable salt of the compound. The compound disclosed by the invention can be used as the nano delivery system based on tumor microenvironment specific response, has good solubility in an aqueous solution, can be self-assembled with a drug in the aqueous solution to form a relatively stable nano compound, can effectively deliver the loaded drug to a tumor site; and can responsively disassembl the nano-drug delivery carrier under corresponding stimulation to achieve the purpose of accurate drug release, so that the drug can be released to the focus part to the greatest extent, and the compound is a novel nano-delivery carrier.

Two-step three-component process for one-pot synthesis of 8-alkylmercaptocaffeine derivatives

Rad, M. N. Soltani,Maghsoudi

, p. 70335 - 70342 (2016/08/06)

A highly efficient, odourless and two-step three-component process for one-pot synthesis of some 8-alkylmercaptocaffeine derivatives has been described. The catalyst-free three-component reaction of alkyl bromides, thiourea, and 8-bromocaffeine gave 8-alkylmercaptocaffeine products in excellent to quantitative yields. In addition, the impact of parameters on sample reaction is discussed.

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