N,N'-Dibenzylethane-1,2-diamine

Identification

Molecular formula

C₁₆H₂₀N₂

CAS number

140-29-4

IUPAC name

acetic acid;N,N'-dibenzylethane-1,2-diamine

State

At room temperature, N,N'-Dibenzylethane-1,2-diamine is a liquid. Due to its oily nature, it is often used in laboratory contexts and can be handled as such with appropriate precautions.

Melting point (Celsius)

13.00

Melting point (Kelvin)

286.15

Boiling point (Celsius)

315.00

Boiling point (Kelvin)

588.15

General information

Molecular weight

240.36g/mol

Molar mass

240.3550g/mol

Density

1.0100g/cm³

Appearence

N,N'-Dibenzylethane-1,2-diamine typically appears as a colorless to pale yellow liquid when in its pure form. It has an oily consistency and may develop a slightly yellowish tint over time due to oxidation or impurities. The compound might have a slight amine-like odor.

Comment on solubility

Solubility of Acetic Acid; N,N'-Dibenzylethane-1,2-diamine

Understanding the solubility of acetic acid; N,N'-dibenzylethane-1,2-diamine reveals fascinating insights into its behavior in various solvents. Here are some key points:

Acetic Acid: This compound is highly soluble in water due to its ability to form hydrogen bonds. Its molecular structure features a polar carboxyl group that interacts favorably with water molecules.
Dibenzylethane-1,2-diamine: This compound exhibits limited solubility in water, primarily due to its larger hydrophobic benzyl groups. However, it is generally more soluble in organic solvents such as ethanol and acetone. The presence of amine groups does enhance solubility to some extent.

When considering the overall solubility of the mixture:

In water, the mixture may display unique properties due to the interaction between the polar acetic acid and the less polar dibenzylethane-1,2-diamine.
In organic solvents, the mixture is likely to combine more homogeneously, improving overall solubility.

In conclusion, while acetic acid thrives in aqueous environments, the presence of N,N'-dibenzylethane-1,2-diamine can complicate its solubility profile. As stated, "Solubility is a dance between polar and non-polar interactions," making this compound an intriguing subject for further investigation.

Interesting facts

Acetic Acid and N,N'-Dibenzylethane-1,2-diamine: An Intriguing Duo

In the realm of organic chemistry, the combination of acetic acid and N,N'-dibenzylethane-1,2-diamine presents a fascinating study in reactivity and functional versatility. Here are some interesting facts about each compound:

Acetic Acid

Common Vinegar Component: Acetic acid is the primary component of vinegar, giving it its pungent smell and sour taste.
Carboxylic Acid: As a simple carboxylic acid, acetic acid is widely used in the chemical industry as a precursor to various synthetic compounds.
Biosynthesis: It plays a pivotal role in biological systems, particularly in cellular respiration where it is involved in the synthesis of acetyl-CoA.
Solvent and Reagent: Acetic acid is used as a solvent and is a key reagent in various organic synthesis reactions, including the production of esters.

Versatile Building Block: This compound serves as a versatile building block in organic synthesis and can be employed in the formation of various derivatives.
Complexation Agent: It exhibits properties that allow it to act as a complexing agent in coordination chemistry, often making it valuable in creating novel coordination compounds.
Pharmaceutical Applications: Compounds related to N,N'-dibenzylethane-1,2-diamine are being explored for their potential use in medicinal chemistry due to their biological activity.

The interaction between these two compounds can lead to interesting reactions, showcasing the importance of reactive functional groups in organic chemistry. Chemical reactions involving acetic acid often produce unique outcomes, and when paired with the structural complexity of N,N'-dibenzylethane-1,2-diamine, the potential for innovation in synthesis and application is significantly increased.

From a student's perspective, studying these compounds not only enhances understanding of organic reaction mechanisms but also highlights the importance of functional groups in determining the chemical behavior of molecules. The interplay between acidity and amine reactivity in different chemical environments makes them a particularly enriching topic.

Synonyms

122-75-8

N,N'-Dibenzylethylenediamine diacetate

Benzathine diacetate

1,2-Ethanediamine, N,N'-bis(phenylmethyl)-, diacetate

1,2-Ethanediamine, N1,N2-bis(phenylmethyl)-, acetate (1:2)

X18B8X2C22

DTXSID40883314

NSC-33274

RefChem:411930

DTXCID901022852

204-572-4

N1,N2-Dibenzylethane-1,2-diamine diacetate

N,N'-Dibenzyl ethylenediamine diacetate

DBED diacetate

MFCD00040588

C20H28N2O4

1,2-Di(benzylamino)ethane diacetate

N,N'-Dibenzylethylenediamine Diacetate Salt

acetic acid;N,N'-dibenzylethane-1,2-diamine

N,N'-Dibenzylethylenediammonium di(acetate)

EINECS 204-572-4

NSC 33274

UNII-X18B8X2C22

N,N-Dibenzyl ethylenediamine dicetic acid

17679-63-9

EC 204-572-4

SCHEMBL8769245

BENZATHINE DIACETATE [MI]

AKOS016004668

CS-W019565

FD36977

N,N\'-Dibenzyl ethylenediamine diacetate

AS-12384

SY036164

N,N'-dibenzylethane-1,2-diamine diacetate

N1,N2-Dibenzylethane-1,2-diaminediacetate

D0280

C90953

EN300-1660866

N pound notN'-Dibenzyl ethylenediamine diacetate

N1,N2-DIBENZYL ETHYLENEDIAMINE DIACETATE

F986631

bis(acetic acid); benzyl[2-(benzylamino)ethyl]amine

Q27293293

Z1741980863

N,N inverted exclamation mark -Dibenzylethylenediamine Diacetate