N-Boc-Ethylenediamine Chemical Properties

Boiling point:

72-80 °C0.1 mm Hg(lit.)

Density 

1.012 g/mL at 20 °C(lit.)

refractive index 

n20/D 1.458(lit.)

Flash point:

>230 °F

storage temp. 

Keep in dark place,Inert atmosphere,2-8°C

solubility 

Chloroform (Slightly), Methanol (Slightly)

form 

Oily Liquid

pka

12.40±0.46(Predicted)

Specific Gravity

1.012

color 

Clear colorless to very light yellow

Water Solubility 

Miscible with methanol and chloroform. Slightly miscible with water.

Sensitive 

Air Sensitive

BRN 

1932330

Exposure limits

ACGIH: TWA 100 ppm
OSHA: TWA 100 ppm(300 mg/m3)
NIOSH: IDLH 1600 ppm; TWA 100 ppm(300 mg/m3); STEL 150 ppm(450 mg/m3)

InChIKey

AOCSUUGBCMTKJH-UHFFFAOYSA-N

CAS DataBase Reference

57260-73-8(CAS DataBase Reference)

Safety Information

Hazard Codes 

C

Risk Statements 

34

Safety Statements 

26-36/37/39-45

RIDADR 

UN 2735 8/PG 3

WGK Germany 

3

F 

10-34

Hazard Note 

Corrosive/Air Sensitive

HazardClass 

8

PackingGroup 

III

HS Code 

29241990

MSDS

• Language:English Provider:SigmaAldrich
• Language:English Provider:ALFA

N-Boc-Ethylenediamine Usage And Synthesis

Chemical Properties

Clear colorless to very light yellow oily liquid

Uses

suzuki reaction

Uses

N-Boc-ethylenediamine is used in the synthesis of thyronamine derivatives. It is also used in the preparation of (2-isothiocyanato-ethyl)-carbamic acid tert-butyl ester by reacting with carbon disulfide. Further, it is used in both oligonucleotide and peptide synthesis.

Uses

N-Boc-ethylenediamine is used in the synthesis of Thyronamine derivatives and analogs.

N-Boc-Ethylenediamine(57260-73-8)Related Product Information

• tert-Butyl glycinate
• tert-Butanol
• tert-Butyl peroxybenzoate
• N-(1-Naphthyl)ethylenediamine dihydrochloride
• Butyl formate
• 2-(2-Aminoethylamino)ethanol
• tert-Butyl 4-aminobenzoate
• 4-Aminobenzoic acid
• N,N,N',N'-Tetramethylethylenediamine
• Methyl acrylate
• Urethane
• Buprofezin
• Dibutyl phthalate
• tert-Butyl carbazate
• tert-Butyl acetate
• Chlorpropham
• Cyhalofop-butyl
• Diisobutyl phthalate