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Octadecyl carbamimidothioate is a chemical compound with the molecular formula C19H38N2S. It is an organic compound that belongs to the class of carbamimidothioates, which are derivatives of carbamic acid. octadecyl carbamimidothioate is characterized by a long aliphatic chain (octadecyl) attached to a carbamimidothioate group, which consists of a nitrogen atom double-bonded to a sulfur atom and a carbonyl group. Octadecyl carbamimidothioate is used in various applications, such as in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals. It is also known for its potential use as a fungicide, indicating its biocidal properties. The compound's long-chain structure contributes to its surfactant-like properties, which can affect its solubility and interaction with other molecules in different environments.

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  • 5397-08-0 Structure
  • Basic information

    1. Product Name: octadecyl carbamimidothioate
    2. Synonyms: carbamimidothioic acid, octadecyl ester
    3. CAS NO:5397-08-0
    4. Molecular Formula: BrH*C19H40N2S
    5. Molecular Weight: 328.5993
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 5397-08-0.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 430.7°C at 760 mmHg
    3. Flash Point: 214.3°C
    4. Appearance: N/A
    5. Density: 0.95g/cm3
    6. Vapor Pressure: 1.27E-07mmHg at 25°C
    7. Refractive Index: 1.499
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: octadecyl carbamimidothioate(CAS DataBase Reference)
    11. NIST Chemistry Reference: octadecyl carbamimidothioate(5397-08-0)
    12. EPA Substance Registry System: octadecyl carbamimidothioate(5397-08-0)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 5397-08-0(Hazardous Substances Data)

5397-08-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5397-08-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,9 and 7 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 5397-08:
(6*5)+(5*3)+(4*9)+(3*7)+(2*0)+(1*8)=110
110 % 10 = 0
So 5397-08-0 is a valid CAS Registry Number.

5397-08-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name octadecyl carbamimidothioate,hydrobromide

1.2 Other means of identification

Product number -
Other names S-Octadecyl-isothioharnstoff,Hydrobromid

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:5397-08-0 SDS

5397-08-0Relevant articles and documents

Introduction of isothiuronium surfactant series: Synthesis, structure-dependent aggregation overview and biological activity

Valeeva,Karimova,Pavlov,Bakhtiyarov,Sapunova,Ivshin,Kataeva,Gaynanova,Syakaev,Voloshina,Galkina,Latypov, Sh.K.,Zakharova, L.Ya.

, (2020/11/20)

For a homologous series of isothiuronium surfactants (S-alkylisothiuronium bromides, CnSU, where n = 10, 12, 14, 16, 18), a synthesis procedure is described and aggregation properties are comprehensively characterized by a variety of techniques. Krafft temperature and critical micelle concentration (cmc) are obtained by methods of conductometry, tensiometry, spectrophotometry, fluorimetry. Using dynamic light scattering and NMR diffusometry, aggregate sizes in aqueous solutions were determined. The aggregation numbers of CnSU systems were estimated by alternative methods. An increase in the length of the alkyl tail from 10 to 16 carbon atoms leads to a decrease in cmc from 16 to 0.5 mM with a decrease in aggregation numbers. S-alkylisothiuronium bromides exhibit solubilization capacity toward a hydrophobic dye Orange OT which is 2–3 times higher than that of alkyltrimethylammonium analogues. Improved solubilization characteristics along with antimicrobial properties manifested at the concentrations of low hemolytic activity allow us to recommend these amphiphiles for the fabrication of soft nanocontainers for hydrophobic guests showing their own biological functionality.

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