Interesting facts
Interesting Facts About 2-Octylsulfanylethanol
2-Octylsulfanylethanol is a fascinating chemical compound that plays a significant role in various applications due to its unique properties. Here are some intriguing facts about this compound:
- Structure and Composition: This compound consists of a long-chain octyl group, which imparts hydrophobic characteristics, alongside a sulfanyl (thioether) and alcohol functional group that contribute to its reactivity and solubility in certain environments.
- Applications: 2-Octylsulfanylethanol is utilized in several industries, including:
- Cosmetics, as an emollient and skin conditioning agent.
- Pharmaceuticals, being explored for its potential antimicrobial properties.
- Research, where it serves as a model compound for studying interactions involving thiol groups.
- Biological Relevance: Compounds like 2-octylsulfanylethanol can act as surfactants, influencing biological membranes and affecting permeability and transport processes in cells.
- Environmental Impact: As a chemical with a long chain, it poses unique challenges regarding biodegradability and accumulation in various ecosystems. Scientists are investigating its environmental fate to ensure its safe use.
- Analogous Compounds: This compound is related to other sulfanyl alcohols, which are crucial in organic synthesis and materials science, showcasing the diverse applications of thiol compounds in innovation.
With its intriguing characteristics and potential applications, 2-octylsulfanylethanol is worthy of study, as it highlights the relationship between molecular structure and functionality in the realm of chemistry.
Synonyms
2-(Octylthio)ethanol
3547-33-9
ETHANOL, 2-(OCTYLTHIO)-
2-Hydroxyethyl octyl sulfide
MGK repellent 874
R-874 phillips
MGK repellent R-874
2-Hydroxyethyl n-octyl sulfide
2-(Oktylthio)ethanol
MGK 874
Caswell No. 489B
R-874
2-(Oktylthio)ethanol [Czech]
2-Hydroxyethyl-n-octyl sulfide
NSC 163967
MGK R-874
R 874
EINECS 222-598-4
2-Hydroxyethyl octyl sulphide
EPA Pesticide Chemical Code 046301
BRN 1698968
DTXSID6032516
UNII-3G5X52121W
AI3-24828
3G5X52121W
NSC-163967
DTXCID4012516
EC 222-598-4
4-01-00-02434 (Beilstein Handbook Reference)
.beta.-Hydroxyethyl n-octyl sulfide
HYDROXYETHYL OCTYL SULFIDE, 2-
HYDROXYETHYL OCTYL SULPHIDE, 2-
beta-Hydroxyethyl n-octyl sulfide
222-598-4
kxpxknbdcuoenf-uhfffaoysa-n
2-(octylsulfanyl)ethan-1-ol
2-hydroxyethyl n-octyl sulphide
2-octylsulfanylethanol
2-(Octylsulfanyl)ethanol
CHEBI:82020
2-Hydroxyethyl-n-octyl sulphide
2(n-Octylthio)ethanol
2-hydroxyethyloctylsulfide
2-(Octylsulfanyl)ethanol #
SCHEMBL39565
WLN: Q2S8
CHEMBL3183276
2-(Hydroxyethyl)n-octyl sulfide
DAA54733
Tox21_301965
2-(OCTYLSULFANYL)-1-ETHANOL
MFCD00014046
NSC163967
STK675268
AKOS005593634
NCGC00255272-01
AS-60429
CAS-3547-33-9
DB-048822
CS-0309383
NS00001693
A10652
C18863
EN300-180400
A822833
Q27155693
Z425753146
2-(Octylsulfanyl)ethan-1-ol, PESTANAL(R), analytical standard
Solubility of 2-octylsulfanylethanol
2-octylsulfanylethanol, with its unique structure, showcases interesting solubility properties. This compound is generally characterized by being:
It's important to note that the solubility of 2-octylsulfanylethanol can be influenced by a variety of factors such as:
In summary, while 2-octylsulfanylethanol exhibits some level of solubility in water, it thrives in organic solvents, emphasizing the classic rule of thumb in chemistry: “like dissolves like.”