3-Isopropoxypropylamine

Names

[ Name ]:
3-Isopropoxypropylamine

[Synonym ]:
3-Aminopropyl Isopropyl Ether
EINECS 220-816-2
3-isopropoxypropan-1-amine
3-isopropyloxypropylamine
1-Amino-3-isopropoxy-propan
3-Isopropoxy-1-propylamine
MFCD00008220
Isopropoxypropylamine
3-Isopropoxy-n-propylamine
3-Isopropoxypropylamine

Chemical & Physical Properties

[ Density]:
0.845 g/mL at 25 °C(lit.)

[ Boiling Point ]:
78-79 °C85 mm Hg(lit.)

[ Melting Point ]:
-65 °C

[ Molecular Formula ]:
C₆H₁₅NO

[ Molecular Weight ]:
117.18900

[ Flash Point ]:
42 °C

[ Exact Mass ]:
117.11500

[ PSA ]:
35.25000

[ LogP ]:
1.46050

[ Vapour Pressure ]:
5.63mmHg at 25°C

[ Index of Refraction ]:
n20/D 1.4195(lit.)

[ Storage condition ]:
Flammables area

[ Water Solubility ]:
miscible

MSDS

Click to get detail MSDS

Safety Information

[ Symbol ]:

GHS02, GHS05

[ Signal Word ]:
Danger

[ Hazard Statements ]:
H226-H314

[ Precautionary Statements ]:
P280-P305 + P351 + P338-P310

[ Personal Protective Equipment ]:
Faceshields;full-face respirator (US);Gloves;Goggles;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter

[ Hazard Codes ]:
C:Corrosive;

[ Risk Phrases ]:
R10;R34

[ Safety Phrases ]:
S16-S23-S26-S27-S36/37/39-S45

[ RIDADR ]:
UN 2734 8/PG 1

[ WGK Germany ]:
1

[ Packaging Group ]:
III

[ Hazard Class ]:
3

[ HS Code ]:
2922199090

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

DownStream

Customs

[ HS Code ]: 2922199090

[ Summary ]:
2922199090. other amino-alcohols, other than those containing more than one kind of oxygen function, their ethers and esters; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

Articles

Synthesis and antibacterial activity of 1-alkoxyalkyl-5-aryl-4-acyl-3-hydroxy-3-pyrrolin-2-ones. Gein VL, et al.

Pharmaceut. Chem. J. 41(4) , 208-210, (2007)

Itaconic acid derivatives of sulfanilamide. Paytash PL, et al.

J. Am. Chem. Soc. 74(18) , 4549-4552, (1952)

Ethyl 1, 4-dihydro-4-oxo-3-quinolinecarboxylates by a tandem addition-elimination-SNAr reaction. Bunce RA, et al.

J. Heterocycl. Chem. 48(3) , 620-625, (2011)