p-Tolylmethanol | Solubility of Things

Identification

Molecular formula

C₈H₁₀O

CAS number

620-17-7

IUPAC name

p-tolylmethanol

State

At room temperature, p-Tolylmethanol is primarily a solid. However, depending on the purity and exact conditions, it may also exist as a viscous liquid.

Melting point (Celsius)

61.00

Melting point (Kelvin)

334.15

Boiling point (Celsius)

222.00

Boiling point (Kelvin)

495.15

General information

Molecular weight

122.17g/mol

Molar mass

122.1650g/mol

Density

1.0145g/cm³

Appearence

Appearance: p-Tolylmethanol is typically a white crystalline solid. It can also appear as a colorless, viscous liquid at higher temperatures.

Comment on solubility

Solubility of p-tolylmethanol

p-tolylmethanol, with the chemical formula C₈H₁₀O, exhibits interesting solubility characteristics that are pertinent for various applications in organic chemistry.

Solubility in Common Solvents:

Water: p-tolylmethanol is sparingly soluble in water due to its hydrophobic portions.
Organic solvents: It is more soluble in organic solvents such as ethanol, methanol, and acetone, making it versatile in laboratory settings.
Non-polar solvents: The compound shows good solubility in non-polar solvents like hexane and toluene.

Factors Influencing Solubility:

Polarity: Due to its molecular structure, p-tolylmethanol's solubility is largely influenced by the polarity of the solvent used.
Temperature: As with many organic compounds, an increase in temperature generally leads to an increase in solubility.
Presence of Other Solutes: The solubility can be further affected by the presence of salts or other solutes in the solvent.

To summarize, the solubility of p-tolylmethanol is relatively limited in polar solvents like water but significantly enhances in organic and non-polar solvents, thus allowing for a wide range of practical applications in the field of organic synthesis and formulation.

Interesting facts

Interesting Facts About p-Tolylmethanol

p-Tolylmethanol, also known as 4-Tolylmethanol, is an organic compound that has caught the attention of chemists and researchers due to its unique properties and applications. Here are some fascinating insights into this compound:

Structure & Functionality: The molecule features a phenolic structure due to the presence of a tolyl group, giving it interesting reactivity. The hydroxyl group facilitates hydrogen bonding, making it useful in various chemical reactions.
Applications in Organic Synthesis: p-Tolylmethanol serves as an important intermediate in organic synthesis. It is used extensively in the preparation of pharmaceuticals, agrochemicals, and other industrial chemicals.
Chiral Center: The compound contains a chiral center, allowing the potential for enantiomer separation. This characteristic is significant in the field of asymmetric synthesis where the production of specific enantiomers is desired for drug development.
Functional Group Manipulation: The hydroxyl group in p-tolylmethanol can undergo various transformations, opening avenues for creating more complex molecules. For instance, it can be converted into p-tolylmethyl chloride, extending its utility in synthetic chemistry.
Biological Relevance: Some studies suggest that components related to p-tolylmethanol may have biological activity. Understanding these properties could lead to the development of new therapies or agricultural products.
Environmental Considerations: As with many organic compounds, p-tolylmethanol’s effects on the environment are an area of study. Its degradation products and potential toxicity are essential aspects to consider in its application.

In conclusion, p-tolylmethanol is not just an ordinary organic compound; its unique structural properties and versatility in applications make it a subject of interest in both academic and industrial research. As the scientific community continues to explore the depths of organic chemistry, compounds like p-tolylmethanol pave the way for innovations that can have far-reaching impacts.

Synonyms

4-Methylbenzyl alcohol

p-Tolylmethanol

589-18-4

(4-Methylphenyl)methanol

Benzenemethanol, 4-methyl-

alpha-Hydroxy-p-xylene

p-Methyl benzyl alcohol

p-Methylbenzylalcohol

4-Methyl-benzenemethanol

p-Methylbenzylalkohol

p-Methylbenzylalkohol [German]

NSC 3992

CCRIS 5112

EINECS 209-639-1

a-Hydroxy-p-xylene

UNII-EXZ915A627

BRN 1856550

CHEBI:1895

DTXSID5025574

AI3-09610

HSDB 7615

EXZ915A627

NSC-3992

(4-TOLYL)METHANOL

4-Methylbenzenemethanol, 9CI

DTXCID205574

1-hydroxymethyl-4-methylbenzene

4-Methyl-1-hydroxymethylbenzene

FEMA NO. 4624

4-Methyl-benzenemethanol (9CI)

METHYL BENZYL ALCOHOL, P-

4-06-00-03171 (Beilstein Handbook Reference)

4-METHYLBENZYL ALCOHOL [HSDB]

pTolualcohol

pTolylcarbinol

pToluic alcohol

pToluyl alcohol

4Tolylcarbinol

pMethylbenzylalcohol

pMethylbenzylalkohol

4methylbenzylalcohol

pMethylbenzyl alcohol

p-methylbenzylalkoohol

4Methylbenzenemethanol

Methylbenzylalcohol, p

pMethyl benzyl alcohol

4Methyl benzenemethanol

(4Methylphenyl)methanol

4(Hydroxymethyl)toluene

Benzyl alcohol, pmethyl

Benzenemethanol, 4methyl

Para-methylbenzyl alcohol

4Methylbenzenemethanol (9CI)

p-methylbenzylalkoohol (German)

209-639-1

inchi=1/c8h10o/c1-7-2-4-8(6-9)5-3-7/h2-5,9h,6h2,1h

kmtdmtzbnygunx-uhfffaoysa-n

p-tolyl alcohol

ptolyl alcohol

p-Tolylcarbinol

P-METHYLBENZYL ALCOHOL

4-Tolylcarbinol

4-(Hydroxymethyl)toluene

4-methylbenzylalcohol

Benzyl alcohol, p-methyl-

p-Toluyl alcohol

4-methylbenzenemethanol

4-methyl-benzyl alcohol

4-Methyl benzenemethanol

31831-37-5

Xylene-alpha-ol

ar-Methylbenzenemethanol

p-tolyl-methanol

4-(Hydroxymethyl)toluene; 4-Methylbenzyl alcohol; p-Methylbenzyl alcohol; p-Tolylcarbinol

4-Tolyl carbinol

MFCD00004664

P-TOLUALCOHOL

4-methyl-benzylalcohol

P-TOLUIC ALCOHOL

(4-methylphenyl)-methanol

bmse000520

SCHEMBL3337

(4-Methylphenyl)methanol #

CHEMBL90100

4-Methylbenzyl alcohol, 98%

NSC3992

Tox21_200089

AKOS000249530

CS-W016577

FM50065

NCGC00091215-01

NCGC00091215-02

NCGC00257643-01

AC-13074

CAS-589-18-4

DB-306080

M0162

NS00012124

EN300-49120

C06757

D77794

Q27067434

VTG