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Merck
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348554

Sigma-Aldrich

3,3′-Iminobis(N,N-dimethylpropylamine)

97%

Sinónimos:

(3-[[3-(Dimethylamino)propyl]amino]propyl)dimethylamine, 1,1,9,9-Tetramethyl-1,5,9-triazanonane, 2,10-Dimethyl-2,6,10-triazaundecane, Bis[3-(dimethylamino)propyl]amine, N,N,N′,N′-Tetramethyldipropylenetriamine, N,N,N′,N′-Tetramethyliminobispropylamine, N,N-Bis[3-(dimethylamino)propyl]amine, N-(3-Dimethylaminopropyl)-N′,N′-dimethylpropane-1,3-diamine, Tetramethyldipropylenetriamine

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About This Item

Fórmula lineal:
HN[(CH2)3N(CH3)2]2
Número de CAS:
6711-48-4
Peso molecular:
187.33
EC Number:
229-761-9
MDL number:
MFCD00014880
UNSPSC Code:
12352100
PubChem Substance ID:
24861585
NACRES:
NA.22

assay

97%

form

liquid

refractive index

n20/D 1.449 (lit.)

bp

128-131 °C/20 mmHg (lit.)

mp

−78 °C (lit.)

density

0.841 g/mL at 25 °C (lit.)

SMILES string

CN(C)CCCNCCCN(C)C

InChI

1S/C10H25N3/c1-12(2)9-5-7-11-8-6-10-13(3)4/h11H,5-10H2,1-4H3

InChI key

BXYVQNNEFZOBOZ-UHFFFAOYSA-N

Application

3,3′-Iminobis(N,N-dimethylpropylamine) may be used:
  • in the synthesis of dimeric quaternary alkylammonium conjugates of sterols
  • as nitrogen containing tridentate lignand in the preparation of [3,3′-iminobis(N,N-dimethylpropylamine)](4′-methoxyflavonolato)zinc(II) perchlorate complex
  • in the preparation of 2-[[[N,N-bis[3-(N,N-dimethylamino)propyl]amino]carbonyl]-1-methyl-4-nitropyrrole and 3-(9-anthracenyl)- N,N-bis[3-(N,N-dimethylamino)propyl]-5-methyl-4-isoxazole carboxamide

pictograms

Skull and crossbonesCorrosion
GHS06,GHS05

signalword

Danger

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 4 Oral - Skin Corr. 1B

Storage Class

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk_germany

WGK 2

flash_point_f

208.4 °F - closed cup

flash_point_c

98 °C - closed cup

ppe

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

Certificados de análisis (COA)

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Bogumił Brycki et al.
Molecules (Basel, Switzerland), 19(7), 9419-9434 (2014-07-06)
New dimeric quaternary alkylammonium conjugates of sterols were obtained by two step reactions of ergosterol, cholesterol and cholestanol with bromoacetic acid bromide, followed by bimolecular nucleophilic substitution with N,N,N',N'-tetramethyl-1,3-propanediamine, N,N,N',N'',N''-pentamethyldiethylenetriamine and 3,3'-iminobis- (N,N-dimethylpropylamine). The product structures were confirmed by spectral
Xiaochun Han et al.
Bioorganic & medicinal chemistry, 17(4), 1671-1680 (2009-01-27)
The synthesis and in vitro anti-tumor 60 cell lines screen of a novel series of anthracenyl isoxazole amides (AIMs) (While not a strict acronym, the designation AIM is in honor of the memory of Professor Albert I. Meyers.) (22-33) are
[3, 3'-Iminobis (N, N-dimethylpropylamine)](4'-methoxyflavonolato) zinc (II) perchlorate,[Zn (4'-MeOfla)(idpaH)] ClO4.
Balogh-Hergovich E, et al.
Acta Crystallographica Section C, Crystal Structure Communications, 55(4), 557-558 (1999)
Łukasz Łątka et al.
Materials (Basel, Switzerland), 14(4) (2021-02-11)
Polyamide-based nanocomposites containing graphene platelets decorated with poly(acrylamide) brushes were prepared and characterized. The brushes were grafted from the surface of graphene oxide (GO), a thermally conductive additive, using atom transfer radical polymerization, which led to the formation of the
[Toxicity of several aliphatic amines].
G I Sidorin et al.
Gigiena truda i professional'nye zabolevaniia, (11)(11), 50-53 (1984-11-01)

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