ethylenediamine, n-benzyl-

Modify Date: 2024-01-02 09:20:20

ethylenediamine, n-benzyl- Structure
ethylenediamine, n-benzyl- structure
Common Name ethylenediamine, n-benzyl-
CAS Number 4152-09-4 Molecular Weight 150.221
Density 1.0±0.1 g/cm3 Boiling Point 259.5±15.0 °C at 760 mmHg
Molecular Formula C9H14N2 Melting Point N/A
MSDS Chinese USA Flash Point 127.6±24.0 °C
Symbol GHS05
GHS05
Signal Word Danger

 Names

Name N-Benzylethylenediamine
Synonym More Synonyms

 Chemical & Physical Properties

Density 1.0±0.1 g/cm3
Boiling Point 259.5±15.0 °C at 760 mmHg
Molecular Formula C9H14N2
Molecular Weight 150.221
Flash Point 127.6±24.0 °C
Exact Mass 150.115692
PSA 38.05000
LogP 0.84
Vapour Pressure 0.0±0.5 mmHg at 25°C
Index of Refraction 1.542
Water Solubility negligible

 Safety Information

Symbol GHS05
GHS05
Signal Word Danger
Hazard Statements 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 R34
Safety Phrases S23-S26-S36/37/39-S45
RIDADR 2735
Packaging Group III
Hazard Class 8
HS Code 2921590090

 Synthetic Route

 Customs

HS Code 2921590090
Summary 2921590090. other aromatic polyamines and their derivatives; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

 Articles4

More Articles
An anionic nucleophilic catalyst system for the diastereoselective synthesis of trans-beta-lactams.

Org. Lett. 7(16) , 3461-3, (2005)

Trans-disubstituted beta-lactams show increasing utility and prominence in numerous pharmaceutical applications, making their asymmetric synthesis an attractive goal for chemists. We introduce an anio...

A new method for the synthesis of tri-tert-butyl diethylenetriaminepentaacetic acid and its derivatives. Achilefu S, et al.

J. Org. Chem. 65(5) , 1562-1565, (2000)

Application of a-chloroaldoxime O-methanesulfonates to one-pot synthesis of N, N', N?-substituted guanidines via Tiemann rearrangement. Yamamoto Y, et al.

Tetrahedron Lett. 50(42) , 5813-5815, (2009)

 Synonyms

N-benzylethane-1,2-diamine
ethylenediamine, n-benzyl-
N'-benzylethane-1,2-diamine
N-Benzyl-1,2-ethanediamine
1,2-Ethanediamine, N-(phenylmethyl)-
N1-Benzylethane-1,2-diamine
EINECS 223-984-5
MFCD00041896
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