Skip to Content
Merck
CN

Key Documents

View All Documentation

39380

3-(Dimethylamino)-1-propylamine

purum, ≥98.0% (GC)

Synonym(s):

N,N-Dimethyl-1,3-diaminopropane, N,N-Dimethyl-1,3-propanediamine

Sign In to View Organizational & Contract Pricing.

Select a Size

Change View

About This Item

Linear Formula:
(CH3)2N(CH2)3NH2
CAS Number:
109-55-7
Molecular Weight:
102.18
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
329755864
EC Number:
203-680-9
Beilstein/REAXYS Number:
605293
MDL number:
MFCD00008216
Assay:
≥98.0% (GC)
Form:
liquid
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

vapor density

3.6 (vs air)

Quality Level

200

vapor pressure

5 mmHg ( 20 °C)

grade

purum

assay

≥98.0% (GC)

form

liquid

impurities

≤2% water

refractive index

n20/D 1.435 (lit.), n20/D 1.436

bp

133 °C (lit.)

density

0.812 g/mL at 25 °C (lit.)

functional group

amine

SMILES string

CN(C)CCCN

InChI

1S/C5H14N2/c1-7(2)5-3-4-6/h3-6H2,1-2H3

InChI key

IUNMPGNGSSIWFP-UHFFFAOYSA-N

General description

3-(Dimethylamino)-1-propylamine (DMAPA, N,N-dimethyl-1,3-propanediamine) is a dialkylamino alkyl amine. It has been prepared from dimethylamine and acrylonitrile and confirmed by 1H NMR. It participates in the synthesis of bio-based zwitterionic surfactants from waste cooking oil (WCO).

Application

3-(Dimethylamino)-1-propylamine (DMAPA) is suitable reagent used in the following studies:
  • As a cationic moiety to form the ionic liquid, 3-(dimethylamino)-1-propylaminium formate ([DMAPA]FA) which is a potential reagent to extract protein from yeast cells.
  • As an aminating agent in the palladium-catalyzed amination of aryl amines.
  • In the derivatization of pullulan to form cationic pullulan.
  • In the partial modification of poly(styrene-alt-maleic anhydride) to form N-substituted maleimide.
  • As a test compound in the parallel synthesis of alkylamine lipidoids.
  • To cleave the polyamides synthesized by solid phase methods on Boc-β-Ala-PAM resin.
It may be used in the following studies:
  • Synthesis of (N,N-dialkylamino)alkyl-2-amino benzamide by reacting with isatoic anhydride.
  • As a reagent for the anomeric deacetylation of protected sugars.
  • Preparation of bioreducible copolymers used in gene delivery.

Other Notes

Industrial applications

Still not finding the right product?

Explore all of our products under 3-(Dimethylamino)-1-propylamine

signalword

Danger

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Oral - Eye Dam. 1 - Flam. Liq. 3 - Skin Corr. 1B - Skin Sens. 1 - STOT SE 3

target_organs

Respiratory system

Storage Class

3 - Flammable liquids

wgk

WGK 1

flash_point_f

89.6 °F - closed cup

flash_point_c

32 °C - closed cup

ppe

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

Regulatory Information

危险化学品

This item has

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
BCCC9373
BCCC4812
BCCB7136
BCCB4396
BCCB3188

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Exploring the potential of xanthene derivatives as trypanothione reductase inhibitors and chloroquine potentiating agents.
Chibale K, et al
Tetrahedron, 59(13), 2289-2296 (2003)
New antihistaminic agents: Synthesis and evaluation of h 1-antihistaminic actions of 3-[(N,N-dialkylamino) alkyl)-1, 2, 3, 4-tetrahydro-(1H)-thioquinazolin-4 (3H)-ones and their oxo analogues.
Raju MB, et al
Indian Journal of Pharmaceutical Sciences, 69(6), 853-853 (2007)
The Rebirth of Waste Cooking Oil to Novel Bio-based Surfactants.
Zhang QQ, et al.
Scientific Reports, 5 (2015)
View All Related Papers

Global Trade Item Number

SKUGTIN
39380-250ML04061831982091
39380-1L04061831982084