4-Hydroxyamphetamine hydrobromide | Solubility of Things

Identification

Molecular formula

C₉H₁₄BrNO

CAS number

3414-55-9

IUPAC name

4-(2-aminopropyl)phenol;hydrobromide

State

At room temperature, 4-Hydroxyamphetamine hydrobromide is in a solid state. It is stable under normal conditions but should be stored in a dry environment to prevent moisture absorption.

Melting point (Celsius)

181.00

Melting point (Kelvin)

454.15

Boiling point (Celsius)

225.00

Boiling point (Kelvin)

498.15

General information

Molecular weight

216.12g/mol

Molar mass

216.1110g/mol

Density

1.2340g/cm³

Appearence

The compound appears as a white crystalline powder. It is typically odorless and hygroscopic in nature. The powder is fine and uniform, possessing a texture akin to flour.

Comment on solubility

Solubility of 4-(2-aminopropyl)phenol; hydrobromide

The solubility of 4-(2-aminopropyl)phenol; hydrobromide is influenced by various factors. This hydrobromide salt is typically characterized by:

Water Solubility: Generally, hydrobromides tend to be more soluble in water compared to their parent amines. This is due to the ability of the hydrobromide group to ionize in aqueous solutions, enhancing solubility.
Polarity: The presence of the amino group contributes to the polarity of the molecule, which can facilitate interactions with water molecules, thus improving solubility.
Temperature Dependence: Like many salts, the solubility may increase with temperature, allowing for more significant dissolution in heated water.

In terms of practical application, the solubility characteristics mean that 4-(2-aminopropyl)phenol; hydrobromide can be effectively utilized in pharmaceutical preparations where aqueous solutions are necessary. However, it's essential to consider:

The pH of the environment, as extreme acidity or alkalinity may impact solubility.
The presence of other solutes, which can either enhance or inhibit solubilization.

Therefore, understanding the solubility of this compound is critical for its effective use in scientific and industrial applications.

Interesting facts

Interesting Facts about 4-(2-Aminopropyl)phenol Hydrobromide

4-(2-Aminopropyl)phenol hydrobromide is a notable compound within the realm of pharmaceutical chemistry, primarily due to its affiliation with psychoactive substances. Here are some intriguing aspects:

Chemical Significance: This compound is often explored for its potential as a central nervous system stimulant, drawing comparisons with other similar compounds. It is essential for researchers to understand such relationships to develop safer and more effective medications.
Research Applications: Studies involving 4-(2-aminopropyl)phenol hydrobromide may focus on its effects on neurotransmitter systems. This is crucial for unveiling mechanisms underlying various neurological disorders.
Historical Context: Often associated with the development of compounds for enhancing mental alertness and mood, this compound reflects the ongoing quest in pharmacology to find effective tools to combat conditions such as depression and attention disorders.
Synthesis and Derivatives: The methods used to synthesize this compound can lead to a variety of derivatives, which can have diverse and unexpected properties. This versatility is a key area of interest in chemical research.

Overall, the study of 4-(2-aminopropyl)phenol hydrobromide invites both excitement and caution. As with many compounds that affect the brain, understanding dosage, mechanisms of action, and potential side effects is crucial for safe usage in both research and therapeutic contexts.

"Knowledge is a treasure, but practice is the key to it." - Thomas Lackington

Synonyms

HYDROXYAMPHETAMINE HYDROBROMIDE

306-21-8

Predrolon

4-(2-Aminopropyl)phenol hydrobromide

p-Hydroxyamphetamine hydrobromide

Paredrine hydrobromide

Hydroxyamfetamin hydrobromid

Hydroxyamfetamine hbr

hydroxyamfetamine hydrobromide

Hydroxyamphetamine hbr

Phenol,4-(2-aminopropyl)-, hydrobromide (1:1)

Phenol, 4-(2-aminopropyl)-, hydrobromide

EINECS 206-181-4

UNII-59IG47SZ0E

NSC 61065

NSC-61065

2-Amino-1-(4-hydroxyphenyl)propane hydrobromide

3-(p-Hydroxyphenyl)-2-aminopropane hydrobromide

59IG47SZ0E

DTXSID0045961

(+-)-p-(2-Aminopropyl)phenol hydrobromide

Phenol, 4-(2-aminopropyl)-, hbr

beta-(p-Hydroxyphenyl)isopropylamine hydrobromide

Phenol, p-(2-aminopropyl)-, hydrobromide

DTXCID8025961

4-(2-aminopropyl)phenol;hydrobromide

NSC61065

Hydroxyamphetamine hydrobromide (USP)

Hydroxyamphetamine hydrobromide [USP]

140-36-3

NCGC00095233-01

Mycadrine

(+/-)-P-(2-AMINOPROPYL)PHENOL HBR

(+/-)-P-(2-AMINOPROPYL)PHENOL HYDROBROMIDE

PAREMYD COMPONENT HYDROXYAMPHETAMINE HYDROBROMIDE

(+-)-Paredrine hydrobromide

HYDROXYAMFETAMINE HYDROBROMIDE (MART.)

HYDROXYAMFETAMINE HYDROBROMIDE [MART.]

HYDROXYAMPHETAMINE HYDROBROMIDE (USP-RS)

HYDROXYAMPHETAMINE HYDROBROMIDE [USP-RS]

HYDROXYAMPHETAMINE HYDROBROMIDE (USP MONOGRAPH)

HYDROXYAMPHETAMINE HYDROBROMIDE [USP MONOGRAPH]

dl-p-(2-Aminopropyl)phenol hydrobromide

1-p-Hydroxyphenyl-2-aminopropane hydrobromide

Paredrine (TN)

Phenol, p-(2-aminopropyl)-, hydrobromide, (+-)-

Phenol, hydrobromide

component of Paredrine

cid_9377

Hyroxyamfetamine hydrobromide

SPECTRUM211425

MLS002320672

MLS002320674

SCHEMBL221647

Hydrobromide, Hydroxyamphetamine

CHEMBL1200705

OXAMPHETAMINE HYDROBROMIDE

WLN: ZY1&1R DQ &EH

HMS1923C15

Pharmakon1600-00211425

AAA30621

Tox21_111487

NSC760066

p-(2-Aminopropyl)phenol hydrobromide

p-(2-Aminopropyl)phenyl hydrobromide

(+)-4-Hydroxyamphetamine hydrobromide

AKOS040758032

CCG-213716

NSC-760066

(+/-)-4-Hydroxyamphetamine hydrobromide

NCGC00095233-02

CAS-306-21-8

SMR001338818

SMR001338820

HYDROXYAMPHETAMINE HYDROBROMIDE [MI]

NS00079429

HYDROXYAMPHETAMINE HYDROBROMIDE [VANDF]

D04473

HYDROXYAMFETAMINE HYDROBROMIDE [WHO-DD]

EN300-7866760

.beta.-(p-Hydroxyphenyl)isopropylamine hydrobromide

HYDROXYAMPHETAMINE HYDROBROMIDE [ORANGE BOOK]

Q27261708

rac. 4-hydroxy-alpha-methylphenethylamine hydrobromide

HYDROXYAMPHETAMINE HYDROBROMIDE COMPONENT OF PAREMYD

206-181-4