4-(Trans-4-N-Pentylcyclohexyl)Phenol,5PcoC17H26O

4-(Trans-4-N-Pentylcyclohexyl)Phenol,5PcoC17H26O - Names and Identifiers

Name	4-(trans-4-Pentylcyclohexyl)phenol
Synonyms	5PCO 4-PENTYL-CYCLOHEXYL PHENOL 4-(4''-N-PENTYLCYCLOHEXYL)PHENOL P-(TRANS-4-PENTYLCYCLOHEXYL)PHENOL 4-(trans-4-Pentylcyclohexyl)phenol 4-(TRANS-4-N-PENTYLCYCLOHEXYL)PHENOL TRANS-4-(4-PENTYLCYCLOHEXYL)-1-HYDROXYBENZENE 4-(Trans-4-N-Pentylcyclohexyl)Phenol,5PcoC17H26O
CAS	82575-69-7
EINECS	617-360-5
InChI	InChI=1/C17H26O/c1-2-3-4-5-14-6-8-15(9-7-14)16-10-12-17(18)13-11-16/h10-15,18H,2-9H2,1H3/t14-,15-

4-(Trans-4-N-Pentylcyclohexyl)Phenol,5PcoC17H26O - Physico-chemical Properties

Molecular Formula	C17H26O
Molar Mass	246.39
Density	0.961±0.06 g/cm3(Predicted)
Melting Point	138.0 to 142.0 °C
Boling Point	369.5±21.0 °C(Predicted)
Flash Point	195.2°C
Vapor Presure	5.56E-06mmHg at 25°C
Appearance	powder to crystal
Color	White to Almost white
pKa	10.21±0.30(Predicted)
Storage Condition	Inert atmosphere,Room Temperature
Refractive Index	1.514

4-(Trans-4-N-Pentylcyclohexyl)Phenol,5PcoC17H26O - Introduction

4-(trans-4-Pentylcyclohexyl)phenol is an organic compound with the following properties:

1. Appearance: A colorless or light yellow solid.
2. Solubility: Soluble in organic solvents such as ethanol, methanol and chloroform.
3. Melting point: about 50-55°C.
4. chemical properties: belongs to phenolic compounds, so it has some typical characteristics of phenols, such as reacting with alkali to form salt, reacting with aldehyde to generate 1,3,5-three phenol, etc.

4-(trans-4-Pentylcyclohexyl)phenol is mainly used for the following:

1. Flavor: Due to its aromatic properties, it can be used as an ingredient in perfumes, soaps and other fragrances.
2. Surfactant: As a kind of surfactant, it can be used in detergent, shampoo, soap, etc.
3. medicine: has antibacterial and anti-inflammatory effects, can be used in the field of medicine preparations.
4. Other applications: The compound can also be used as additives for dyes, rubber and plastics.

There are two main methods for preparing 4-(trans-4-Pentylcyclohexyl)phenol: synthesis and extraction:

1. synthesis: synthesis by tandem reaction, first of all, the phenol and ethyl bromide action to generate para-substituted, and then with chlorinated valeryl chloride and pentanol reaction to generate substituted cyclohexyl chloride, and finally the above two steps of the product condensation reaction to obtain the target product.
2. Extraction: The compound can be obtained from extracts of certain plants, animals and plants.

In terms of safety information, the toxicity and risk associated with 4-(trans-4-Pentylcyclohexyl)phenol require further evaluation and study. When using the compound should be careful to avoid contact with eyes, skin and inhalation of its dust, such as accidental contact, should immediately rinse with water. At the same time, the principles of rational use and storage of chemicals should be followed to ensure that they are stored in dry, closed containers, away from fire and heat sources. A professional or agency should be consulted for any health and safety concerns regarding the compound.

Last Update：2024-04-09 21:11:58