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N,N',N',3-Tetramethyl-3-azapentane-1,5-diamine is an organic compound with the chemical formula C9H22N2. It is a colorless liquid with a molecular weight of 158.29 g/mol. N,N',N',3-Tetramethyl-3-azapentane-1,5-diamine is characterized by its four methyl groups attached to the nitrogen atoms and the azapentane bridge connecting the two amine groups. It is soluble in water and has a low vapor pressure.

61877-80-3

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61877-80-3 Usage

Uses

Used in Chemical Synthesis:
N,N',N',3-Tetramethyl-3-azapentane-1,5-diamine is used as a building block in the synthesis of various organic compounds, including pharmaceuticals, agrochemicals, and specialty chemicals. Its unique structure and reactivity make it a valuable intermediate in the development of new molecules with specific properties and applications.
Used in Analytical Chemistry:
N,N',N',3-Tetramethyl-3-azapentane-1,5-diamine is used as a regulated fluorescent sensor for transition metal ions. It can form polyazapodands, which are complex structures that can selectively bind and detect specific metal ions. This property makes it useful in environmental monitoring, industrial processes, and research applications where the detection and quantification of metal ions are crucial.
Used in Material Science:
N,N',N',3-Tetramethyl-3-azapentane-1,5-diamine can be used in the development of new materials with unique properties, such as conductive polymers, sensors, and catalysts. Its ability to form stable complexes with metal ions can be exploited to create materials with enhanced performance in various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 61877-80-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,8,7 and 7 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 61877-80:
(7*6)+(6*1)+(5*8)+(4*7)+(3*7)+(2*8)+(1*0)=153
153 % 10 = 3
So 61877-80-3 is a valid CAS Registry Number.

61877-80-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name N'-[2-(dimethylamino)ethyl]-N,N'-dimethylethane-1,2-diamine

1.2 Other means of identification

Product number -
Other names N-(2-dimethylaminoethyl)-N-(2-methylaminoethyl)-methylamine

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:61877-80-3 SDS

61877-80-3Downstream Products

61877-80-3Relevant academic research and scientific papers

Basic proline-amide derivatives of GE 2270 and GE 2270-like antibiotics

-

, (2008/06/13)

PCT No. PCT/EP96/00407 Sec. 371 Date Jul. 31, 1997 Sec. 102(e) Date Jul. 31, 1997 PCT Filed Feb. 1, 1996 PCT Pub. No. WO96/24607 PCT Pub. Date Aug. 15, 1996The present invention refers to basic amides derivatives of GE 2270 and GE 2270-like antibiotics of general formula (1), wherein the group GE represents the antibiotic core molecule. The amide derivatives of antibiotic GE 2270 of formula (I) are antimicrobial agents mainly active against gram positive bacteria.

Basic oxazoline-amide derivatives of GE2270 and GE2270-like antibiotics

-

, (2008/06/13)

The present invention refers to basic oxazoline-amide derivatives of GE 2270 and GE 2270-like antibiotics of general formula (I), wherein the group GE represents the antibiotic core molecule. The amide derivatives of antibiotic GE 2270 of formula (I) are antimicrobial agents mainly active against gram positive bacteria. STR1

Reactions of the butyllithiums with tertiary oligoethylenepolyamines

Luitjes, Hendrikus,Schakel, Marius,Aarnts, Maxim P.,Schmitz, Robert F.,De Kanter, Franciscus J.J.,Klumpp, Gerhard W.

, p. 9977 - 9988 (2007/10/03)

Complexes of t-BuLi monomer with 1,4,7-trimethyl-1,4,7-triazacyclononane (TMTAN, 3-CH3) and tris(N,N-dimethyl-2-aminoethyl)amine (4-CH3) were identified by 13C-NMR. Rapid elimination of LiN(CH2CH2NMe2)2 takes place from the free CH2CH2NMe2 group of t-BuLi·4-CH3. BuLi complexes of hexamethyltriethylenetetramine (5-CH3) and octamethylpenthaethylenehexamine (6) behave similarly, as does 4-CH2Li. Complexes of BuLi oligomers are lithiated at free N-CH3.

N-lithio-N,N',N'',N''-tetramethyldiethylenetriamine and N'-lithio- N,N,N'',N''-tetramethyldiethylenetriamine; oxidative coupling of aminomethyllithium derivatives

Luitjes,Schakel,Klumpp

, p. 2257 - 2261 (2007/10/02)

N-lithio-N,N',N'',N''-tetramethyldiethylenetriamine (I-Li) is formed from 2,5,8,11-tetramethyl-2,5,8,11-tetraazadodecane (III) or from 2,5,8,11,14,17- hexamethyl-2,5,8,11,14,17-hexaazaoctadecane (IV) with n-BuLi or sec-BuLi, respectively, its isomer N'-lithio-N,N,N'',N'',-tetramethyldiethylene- triamine (II-Li) from tris(2-dimethylaminoethyl)amine (V) with n-BuLi. IV results from treatment of N-lithiomethyl-N,N',N'',N''- tetramethyldiethylenetriamine (PMDTA-Li) with 1,2-dibromoethane.

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