112720
N,N-Diethylethylenediamine
≥99%
Synonym(s):
2-Diethylaminoethylamine
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About This Item
Linear Formula:
(C2H5)2NCH2CH2NH2
CAS Number:
Molecular Weight:
116.20
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
202-844-7
Beilstein/REAXYS Number:
605299
MDL number:
Assay:
≥99%
Quality Level
assay
≥99%
refractive index
n20/D 1.436 (lit.)
bp
145-147 °C (lit.)
density
0.827 g/mL at 25 °C (lit.)
functional group
amine
SMILES string
CCN(CC)CCN
InChI
1S/C6H16N2/c1-3-8(4-2)6-5-7/h3-7H2,1-2H3
InChI key
UDGSVBYJWHOHNN-UHFFFAOYSA-N
Application
N,N-Diethylethylenediamine was used in the oxidative amidation of hydrogen phosphonate diesters in the synthesis of oligonucleotides.
N,N-diethylethylenediamine was used to develop melanin targeted PET and single-photon emission computed tomography (SPECT) imaging agents for melanoma.
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Danger
hcodes
Hazard Classifications
Acute Tox. 3 Dermal - Acute Tox. 4 Inhalation - Flam. Liq. 3 - Skin Corr. 1A
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
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Hongguang Liu et al.
Molecular pharmaceutics, 10(9), 3384-3391 (2013-08-10)
Radiofluorinated benzamide and nicotinamide analogues are promising molecular probes for the positron emission tomography (PET) imaging of melanoma. Compounds containing aromatic (benzene or pyridine) and N,N-diethylethylenediamine groups have been successfully used for development of melanin targeted PET and single-photon emission
J M Dagle et al.
Nucleic acids research, 28(10), 2153-2157 (2000-04-25)
We have designed a new class of modified antisense oligodeoxyribonucleotides (ODN) consisting of a central contiguous stretch of 6-8 unmodified nucleotides flanked by 3'- and 5'-regions containing several nucleotides joined by cationic internucleoside linkages. The positive charge results from modification
Diana Salakhieva et al.
International journal of pharmaceutics, 517(1-2), 234-246 (2016-12-10)
A series of 14 cationic derivatives of poly(aspartic acid) i.e. cationic polyaspartamides with different (dialkylamino)alkyl and alkyl or hydroxyalkyl side groups was synthesized by nucleophilic addition on polysuccinimide. The resulting polyaspartamides have moderate amphiphilic properties. Relationships between the structure and
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 112720-100G | 04061838700223 |
| 112720-5G | 04061838700230 |