Tetralin-1-amine | Solubility of Things

Identification

Molecular formula

C₁₀H₁₃N

CAS number

5299-64-9

IUPAC name

tetralin-1-amine

State

Liquid at room temperature.

Melting point (Celsius)

-2.00

Melting point (Kelvin)

271.15

Boiling point (Celsius)

244.00

Boiling point (Kelvin)

517.15

General information

Molecular weight

135.21g/mol

Molar mass

135.2060g/mol

Density

0.9890g/cm³

Appearence

Clear to pale yellow liquid.

Comment on solubility

Solubility of Tetralin-1-amine

Tetralin-1-amine, also known as 1-amino-tetralin, is an organic compound that exhibits interesting solubility characteristics in various solvents. Understanding its solubility is essential for applications in fields such as organic synthesis and pharmaceuticals.

Solubility Characteristics

Tetralin-1-amine demonstrates the following solubility traits:

Polar solvents: It is generally soluble in polar solvents such as water and alcohols, given its amino functional group that can engage in hydrogen bonding.
Non-polar solvents: It shows limited solubility in non-polar solvents due to the presence of the amine group, which thrives in a more polar environment.
pH sensitivity: The solubility can also be affected by pH. At higher pH levels, the amine group can become protonated, which can significantly enhance solubility in aqueous solutions.

As a result, tetralin-1-amine may find better solubility profiles in the following scenarios:

When mixed with polar protic solvents.
In acidic conditions that facilitate protonation.
In mixtures where its hydrophobic tetralin ring structure can interact favorably with other aromatic compounds.

As a final note, the solubility of tetralin-1-amine is a crucial factor to consider when working with this compound, as it can impact reactivity and stability in various chemical processes. The interplay of its functional groups reveals significant insights into its potential applications.

Interesting facts

Interesting Facts About Tetralin-1-amine

Tetralin-1-amine, also known as (1-amino-1,2,3,4-tetrahydronaphthalene), is an intriguing compound that falls within the category of amines. As a scientist or student of chemistry, here are some engaging aspects to consider:

Structural Significance: Tetralin-1-amine features a unique bicyclic structure that combines the naphthalene framework with an amine functional group. This structural complexity is fascinating, as it provides a distinctive set of properties and reactivity that chemists find useful.
Versatile Applications: Due to its structural properties, tetralin-1-amine can be utilized in different fields, including organic synthesis, pharmaceuticals, and materials science. It acts as a building block for more complex molecules, contributing to the development of various chemical entities.
Bioactivity: Similar compounds have shown biological activity, prompting research into the potential pharmacological applications of tetralin-1-amine itself. The study of its derivatives could lead to the discovery of new therapeutic agents.
Reaction Pathways: Chemists can explore various reaction pathways involving tetralin-1-amine. Its amine group makes it nucleophilic, allowing it to undergo substitution and addition reactions, which could be harnessed for synthetic purposes.
Educational Value: In academic settings, tetralin-1-amine serves as an excellent example for illustrating concepts such as chirality, amine reactivity, and molecular geometry. Students can learn about the significance of functional groups and their impact on chemical behavior.

In conclusion, tetralin-1-amine is more than just a chemical compound; it is a gateway into understanding numerous aspects of organic chemistry, showcasing how structural features influence reactivity and application in various scientific domains.

Synonyms

Aminotetralin

Aminotetralin [Czech]

Tetrahydro-beta-naphthylamine

EINECS 220-973-7

beta-1,2,3,4-Tetrahydronaphthylamine

BRN 1102357

2-Amino-1,2,3,4-tetrahydronaftalen [Czech]

2-NAPHTHYLAMINE, 1,2,3,4-TETRAHYDRO-

2-Amino-1,2,3,4-tetrahydronaftalen

4-12-00-02943 (Beilstein Handbook Reference)

3-aminotetralin

3-aminotetraline

2-aminotetrahydronaphthalene

3-aminotetrahydronaphthalene

DTXCID90973239

220-973-7

dtxsid10903058

1,2,3,4-Tetrahydro-1-naphthylamine

2217-40-5

1,2,3,4-tetrahydronaphthalen-1-amine

1-Aminotetralin

(+/-)-1-aminotetralin

1-Amino-1,2,3,4-tetrahydro-naphthalene

MFCD00001740

O7A3GV2PNX

1-Amino-1,2,3,4-tetrahydronaphthalene

NSC-30349

1,2,3,4-tetrahydronaphthalen-1-ylamine

(+/-)-1,2,3,4-TETRAHYDRO-1-NAPHTHYLAMINE

1,2,3,4-Tetrahydro-naphthalen-1-ylamine

Naphthalenamine, 1,2,3,4-tetrahydro-

MFCD00671629

1-aminotetraline

1,2,3,4-tetrahydronaphthylamine

NSC30349

EINECS 218-712-7

NSC 30349

1-Naphthalenamine, 1,2,3,4-tetrahydro-

UNII-O7A3GV2PNX

tetrahydro-1-naphthylamine

UNII-LGX8T83G7X

EC 218-712-7

1,2,3,4-TETRAHYDRONAPHTHALENE-1-AMINE

SCHEMBL40422

(RS)-1-AMINOTETRALIN

SCHEMBL4667951

SCHEMBL14543304

DTXSID70903059

HMS1735D12

ALBB-020892

BCP26855

1,2,3,4-tetrahydro naphthyl amine

1,2,3,4-tetrahydro-1-naphtylamine

STK397313

1-AMINOTETRALIN, (+/-)-

AKOS000113660

AKOS016039381

AB00150

AB06758

AC-5739

CS-W007739

FT00882

SB13761

1,2,3,4-tetrahydro-1-naphthalenylamine

AS-81177

BP-10652

PD179126

rac-1,2,3,4-tetrahydro-1-naphthylamine

SY001972

SY004141

SY045443

1,2,3,4-Tetrahydro-1-naphthalenamine #

DB-045832

1,2,3,4-Tetrahydro-1-naphthylamine, 97%

naphthalene, 1-amino-1,2,3,4-tetrahydro-

NS00002320

racemic 1,2,3,4-tetrahydro-1-naphthylamine

racemic 1,2,3,4-tetrahydro-1-naphtylamine

racemic 1,2,3,4-tetrahydro-l-naphthylamine

S)-1-Amino-1,2,3,4-tetrahydronaphthalene

T1992

T2501

EN300-18939

rac-1,2,3,4-tetrahydro-naphthalen-1-ylamine

(R)-1, 2, 3, 4-tetrahydro-1-naphthylamine

(RS)-1,2,3,4-TETRAHYDRO-1-NAPHTHYLAMINE

Q27285437

F0001-0783

(+/-)-1,2,3,4-TETRAHYDRO-.ALPHA.-NAPHTHYLAMINE

1-NAPHTHALENAMINE, 1,2,3,4-TETRAHYDRO-, (+/-)-