Welcome to LookChem.com Sign In|Join Free

CAS

  • or

638-67-5

Post Buying Request

638-67-5 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

638-67-5 Usage

Chemical Properties

white flakes

Uses

Different sources of media describe the Uses of 638-67-5 differently. You can refer to the following data:
1. Organic synthesis.
2. n-Tricosane is used as a pharmaceutical intermediate.

Definition

ChEBI: A straight chain alkane containing 23 carbon atoms.

General Description

Leafs (ether-alcohol).

Air & Water Reactions

Insoluble in water.

Reactivity Profile

Saturated aliphatic hydrocarbons, such as N-TRICOSANE, may be incompatible with strong oxidizing agents like nitric acid. Charring of the hydrocarbon may occur followed by ignition of unreacted hydrocarbon and other nearby combustibles. In other settings, aliphatic saturated hydrocarbons are mostly unreactive. They are not affected by aqueous solutions of acids, alkalis, most oxidizing agents, and most reducing agents. When heated sufficiently or when ignited in the presence of air, oxygen or strong oxidizing agents, they burn exothermically to produce carbon dioxide and water.

Check Digit Verification of cas no

The CAS Registry Mumber 638-67-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,3 and 8 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 638-67:
(5*6)+(4*3)+(3*8)+(2*6)+(1*7)=85
85 % 10 = 5
So 638-67-5 is a valid CAS Registry Number.
InChI:InChI=1/C23H48/c1-3-5-7-9-11-13-15-17-19-21-23-22-20-18-16-14-12-10-8-6-4-2/h3-23H2,1-2H3

638-67-5 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • Alfa Aesar

  • (A14577)  n-Tricosane, 99%   

  • 638-67-5

  • 5g

  • 463.0CNY

  • Detail
  • Alfa Aesar

  • (A14577)  n-Tricosane, 99%   

  • 638-67-5

  • 25g

  • 1979.0CNY

  • Detail
  • Alfa Aesar

  • (A14577)  n-Tricosane, 99%   

  • 638-67-5

  • 100g

  • 7449.0CNY

  • Detail
  • Supelco

  • (442712-U)  Tricosane  analytical standard

  • 638-67-5

  • 442712-U

  • 669.24CNY

  • Detail
  • Aldrich

  • (263850)  Tricosane  99%

  • 638-67-5

  • 263850-1G

  • 296.01CNY

  • Detail
  • Aldrich

  • (263850)  Tricosane  99%

  • 638-67-5

  • 263850-5G

  • 569.79CNY

  • Detail

638-67-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name tricosane

1.2 Other means of identification

Product number -
Other names Succinimide,N-(trichloromethylthio)

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:638-67-5 SDS

638-67-5Downstream Products

638-67-5Relevant articles and documents

Identification and synthesis of the male-produced sex pheromone of the soldier beetle chauliognathus fallax (Coleoptera: Cantharidae)

Vidal, Diogo M.,Fávaro, Carla F.,Guimar?es, Matheus M.,Zarbin, Paulo H. G.

, p. 1506 - 1511 (2016/08/10)

Chauliognathus fallax Germar 1824 (Coleoptera: Cantharidae) occurs in North and South America and Australia. Gas chromatographic (GC) analyses of volatiles released by adults showed the presence of a male specific compound. GC coupled with electroantennographic detection (GC-EAD) showed that this compound is exclusively bioactive on female antennae, suggesting it to be a sex pheromone. GC coupled with mass spectrometry (GC-MS) and Fourier transform infrared spectroscopy (GC-FTIR), as well as dimethyl disulfide (DMDS) derivatization and hydrogenation, suggested the target compound to be (Z)-tricos-11-ene. Unambiguous structural proof was achieved by independent synthesis, whereas the biological significance of the compound as a sex pheromone was confirmed by field bioassays.

DEGRADATION OF POLYCYCLIC AROMATIC HYDROCARBONS TO RENDER THEM AVAILABLE FOR BIODEGRADATION

-

Page/Page column 5-8; 15-16, (2008/12/07)

A method for the degradation of polycyclic aromatic compounds is disclosed that involves dissolving ozone in a bipolar solvent comprising a non-polar solvent in which is of sufficiently non-polar character to solubilized the polycyclic aromatic compounds, and a polar-water-compatible solvent which is fully miscible with the non-polar solvent to form a single phase with the non-polar solvent. The bipolar solvent with dissolved ozone is contacted with the polycyclic aromatic compounds to solubilize the polycyclic aromatic compounds and react the dissolved polycyclic aromatic compounds with the ozone to degrade the dissolved polycyclic aromatic compounds to oxygenated intermediates. The bipolar solvent is then mixed with sufficient water to form separate non-polar and polar phases, the non-polar phase comprising the non-polar solvent and the polar phase comprising the non-polar solvent and the oxygenated intermediates. The polar phase is then diluted and incubated with bacteria to biodegrade the oxygenated intermediates.

Composition and process for augmenting, enhancing or imparting a leather aroma to consumable materials

-

, (2008/06/13)

Described is the process for augmenting, enhancing or imparting leather aromas to consumable materials including perfume compositions, colognes, perfumed polymers and perfumed articles including solid or liquid anionic, cationic, nonionic or zwitterionic detergents, fabric softener compositions, fabric softener articles, hair preparations, cosmetic powders and the like, by adding thereto a composition of matter consisting of the following ingredients: "A": At least one substance having the structure: STR1 in an amount of from about 1% up to about 5% wherein R9 represents C9 -C11 straight-chain alkyl and wherein R10 represents methyl and X is a moiety selected from the group consisting of: STR2 "B": At least one compound having the structure: STR3 in an amount of from about 3 up to about 7% wherein each of R12 -R15 represents hydrogen or C1 -C4 alkyl with the proviso that at least two of R12 -R15 represents hydrogen; "C": At least one compound having the structure: STR4 in an amount of from about 2% up to about 6% wherein R1, R2, R3, R4 and R5 each represents hydrogen or C1 -C4 alkyl with the proviso that one, two or three of R1, R2, R3, R4 and R5 represents C1 -C4 alkyl; "D": Optionally, at least one compound having the structure: STR5 in an amount of from 0% up to about 1.2% wherein R6 represents hydrogen or methyl and R11 represents hydrogen or methyl with the proviso that at least one of R6 or R11 is hydrogen; "E": At least one compound defined according to the structure: STR6 in an amount of from about 30% up to about 70% wherein R7 represents C11, C13, or C15 straight-chain alkyl and R8 represents C1 -C3 lower alkyl; "F": At least one compound having the structure: STR7 in an amount of from about 20% up to about 60% wherein n represents an integer of from 8 up to 28; "G": Optionally, the compound having the structure: STR8 in an amount of from 0 up to about 6%; and "H": Optionally, the compound having the structure: STR9 in an amount of from 0 up to about 6% with the requirement that: STR10 equal 100%.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 638-67-5