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N''-Dodecyl-N,N,N',N'-tetramethylguanidine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

25661-96-5

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25661-96-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 25661-96-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,6,6 and 1 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 25661-96:
(7*2)+(6*5)+(5*6)+(4*6)+(3*1)+(2*9)+(1*6)=125
125 % 10 = 5
So 25661-96-5 is a valid CAS Registry Number.
InChI:InChI=1/C17H37N3/c1-6-7-8-9-10-11-12-13-14-15-16-18-17(19(2)3)20(4)5/h6-16H2,1-5H3

25661-96-5SDS

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 2-Dodecyl-1,1,3,3-tetramethylguanidin

1.2 Other means of identification

Product number -
Other names 2-DODECYL-1,1,3,3-TETRAMETHYLGUANIDINE

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:25661-96-5 SDS

25661-96-5Downstream Products

25661-96-5Relevant academic research and scientific papers

Orthoamides and Iminium salts, CIII. Synthesis of N,N′,N′′-persubstituted guanidinium salt-based ionic liquids by anion metathesis

Kantlehner, Willi,Mezger, Jochen,Tiritiris, Ioannis,Kre?, Ralf,Frey, Wolfgang

, (2021/02/26)

N,N′,N′′-peralkylated guanidinium chlorides and N,N′,N′′-peralkylated guanidines were prepared from N,N′-peralkylated chloroformamidinium chlorides. The alkylation of the guanidines affords N,N′,N′′-persubstituted guanidinium chlorides bromides, iodides,

Superbase catalysis of oxazolidin-2-one ring formation from carbon dioxide and prop-2-yn-1-amines under homogeneous or heterogenous conditions

Costa, Mirco,Chiusoli, Gian Paolo,Taffurelli, Davide,Dalmonego, Giulio

, p. 1541 - 1546 (2007/10/03)

N-alkyl-substituted prop-2-yn-1-amines and N-tri-, tetra- and penta-alkyl-substituted guanidines or other strong organic bases assemble under the action of carbon dioxide to afford carbamates, from which methyleneoxazolidinones 2 are formed by ring closure. If alkyl or cycloalkyl chains of appropriate length are present in the guanidines the reaction readily occurs under heterogenous conditions without solvent.

Orthoamides, XL. - Preparation of 1,1,2,3,3-Pentasubstituted and 1,1,2,2,3,3-Hexasubstituted Guanidinium Salts and 1,1,2,3,3-Pentaalkylguanidines

Kantlehner, Willi,Haug, Erwin,Mergen, Walter W.,Speh, Peter,Maier, Thomas,et al.

, p. 108 - 126 (2007/10/02)

N,N,N',N'-(Tetramethyl)thiourea (1) reacts with N,N-dimethylcarbamoyl chloride (2) to give the guanidinium salt 3a.The carbenium salt 4, obtained from 1 and dimethyl sulfate, affords on treatment with dimethylamine the guanidinium salt 3b.Reaction of phosgene with N,N,N',N'-tetraalkylureas yields the chloroformamidinium chlorides 5 which are transformed by mixtures of primary or secondary amines and tertiary amines into mixtures of guanidinium salts and ammonium salts.From these mixtures, by means of sodium hydroxide, have been isolated the guanidinium salts 3a, 6, and 11, respectively.Some of the salts 3a and 6 are converted into the corresponding tetraphenylborates 7.The fluoroborates 8a and 8b are obtained from guanidinium chlorides 3a and 6h, respectively.By anion exchange in 8a, b the salts 9, 10 have been prepared.Alkylation of the guanidines 12 affords the guanidinium salts 13.

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