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TRICOSENE (7Z), also known as triclocarban, is a chlorinated aromatic compound that serves as an effective antimicrobial agent. It is widely used in personal care and consumer products, such as soaps, lotions, and toothpaste, to provide long-lasting protection against bacteria and fungi. However, its potential environmental and health impacts, including contributing to antibiotic resistance and hormone disruption, have led to regulatory scrutiny and restrictions in some countries.

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  • 52078-42-9 Structure
  • Basic information

    1. Product Name: TRICOSENE (7Z)
    2. Synonyms: 7Z-TRICOSENE;TRICOSENE (7Z);7(Z)-Tricosene Exclusive;(Z)-tricos-7-ene
    3. CAS NO:52078-42-9
    4. Molecular Formula: C23H46
    5. Molecular Weight: 322.61134
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 52078-42-9.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: TRICOSENE (7Z)(CAS DataBase Reference)
    10. NIST Chemistry Reference: TRICOSENE (7Z)(52078-42-9)
    11. EPA Substance Registry System: TRICOSENE (7Z)(52078-42-9)
  • 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: 52078-42-9(Hazardous Substances Data)

52078-42-9 Usage

Uses

Used in Personal Care Industry:
TRICOSENE (7Z) is used as an antimicrobial agent in personal care products for its ability to kill bacteria and fungi, ensuring long-lasting protection against germs and maintaining hygiene.
Used in Consumer Products Industry:
TRICOSENE (7Z) is used as an antimicrobial agent in consumer products such as toothpaste to prevent the growth of harmful microorganisms, promoting oral health and reducing the risk of dental infections.
However, due to concerns regarding its potential impact on the environment and human health, some countries have implemented restrictions on the use of TRICOSENE (7Z) in certain products. This has led to the exploration of alternative antimicrobial agents that are safer and more environmentally friendly.

Check Digit Verification of cas no

The CAS Registry Mumber 52078-42-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,0,7 and 8 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 52078-42:
(7*5)+(6*2)+(5*0)+(4*7)+(3*8)+(2*4)+(1*2)=109
109 % 10 = 9
So 52078-42-9 is a valid CAS Registry Number.

52078-42-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 7(Z)-Tricosene

1.2 Other means of identification

Product number -
Other names -

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:52078-42-9 SDS

52078-42-9Downstream Products

52078-42-9Relevant articles and documents

PROCESS FOR PREPARING (7Z)-7-TRICOSENE

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Paragraph 0085; 0092-0100, (2020/12/05)

The present invention provides a process for preparing (7Z)-7-tricosene of the following formula (3): the process comprising a step of subjecting a nucleophilic reagent, (8Z)-8-pentadecenyl compound of the following general formula (1), wherein M1 represents Li, MgZ1, CuZ1 or CuLiZ1, wherein Z1 represents a halogen atom or an (8Z)-8-pentadecenyl group, to a coupling reaction with a 1-halooctane compound of the following general formula (2), wherein X1 represents a halogen atom, to produce (7Z)-7-tricosene (3).

Synthesis of (Z)-7-heneicosene and (Z)-7-tricosene via organoboranes - Part V

Battu, Raminderjit S.,Dhillon, Ranjit S.,Singh, Jasvinder

, p. 1104 - 1105 (2007/10/03)

(Z)-7-Heneicosene 4a and (Z)-7-tricosene 4b, the main components of the female sex pheromones of staphylinid beetle, Aleochara cartula have been synthesized by hydroboration of 1-octyne with BHBr2.SMe2 followed by esterification with a diol and subsequent treatment with Grignard reagent, I2/MeOH and NaOH.

One-pot syntheses of (Z)-7-heneicosene and (Z)-7-tricosene

Singh,Sharma,Vig,Sabharwal

, p. 486 - 486 (2007/10/02)

A new and highly sterospecific synthesis of (Z)-7-heneicosene (I) and (Z)-7-tricosene (II) through hydroboration-hydridation (LAH)-hydroboration with dibromoborane-dimethyl sulphide complex followed by iodine-induced rearrangement is described.

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