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DIMETHYL UREA (DİMETİL ÜRE)

DI METHYL UREA (DİMETİL ÜRE )

SYNONYMS;

1,1-Dimethylharnstoff; dımethyl urea; dimetil üre; dimethyl ürea; dımethyl ure; dimtil ürea; DIMETHYL UREA; dimetily ürea; dimetil üre; DIMETİL ÜRE; DIMETHYL UREA; DIMETYL URE; DIMETHYL REA; dimethyl üre; dimetyl ürea; dimethyl üre; dımethyl urea; (CH3NH)2CO;AKOS B029718;1.3-DiMethyl u;SYM-DIMETHYLUREA;1,3-dimethyl-ure;1,3-DIMETHYLUREA;N,N'-DIMETHYLUREA;n,n'-dimethyl-ure;Dimethylcarbamide; Dimethylurea (DMU; Uses; 1,3-Dimethylurea; DIMETHYL UREA; DIMETYLURE; dimethylürea; dımethyl urea; dimetil üre; dimethyl ürea; dımethyl ure; dimtil ürea; DIMETHYL UREA; dimetily ürea; dimetil üre; DIMETİL ÜRE; DIMETHYL UREA; DIMETYL URE; DIMETHYL REA; dimethyl üre; dimetyl ürea; dimethyl üre; dımethyl urea; (CH3NH)2CO;AKOS B029718;1.3-DiMethyl u;SYM-DIMETHYLUREA;1,3-dimethyl-ure;1,3-DIMETHYLUREA;N,N'-DIMETHYLUREA;n,n'-dimethyl-ure;Dimethylcarbamide; Dimethylurea (DMU; Uses; 1,3-Dimethylurea; DIMETHYL UREA; DIMETYLURE; dimethylürea; dımethyl urea; dimetil üre; dimethyl ürea; dımethyl ure; dimtil ürea; DIMETHYL UREA; dimetily ürea; dimetil üre; DIMETİL ÜRE; DIMETHYL UREA; 1,1-Dimethylurea; DIMETYL URE; DIMETHYL REA; 1,3-Dimethylharnstoff; dimethyl üre; dimetyl ürea; dimethyl üre; dımethyl urea; (CH3NH)2CO;AKOS B029718;1.3-DiMethyl u;SYM-DIMETHYLUREA;1,3-dimethyl-ure;1,3-DIMETHYLUREA;N,N'-DIMETHYLUREA;n,n'-dimethyl-ure;Dimethylcarbamide; Dimethylurea (DMU; Uses; 1,3-Dimethylurea; DIMETHYL UREA; DIMETYLURE; dimethylürea; dımethyl urea; dimetil üre; dimethyl ürea; dımethyl ure; dimtil ürea; DIMETHYL UREA; dimetily ürea; dimetil üre; DIMETİL ÜRE; DIMETHYL UREA; DIMETYL URE; DIMETHYL REA; dimethyl üre; dimetyl ürea; dimethyl üre; dımethyl urea; (CH3NH)2CO;AKOS B029718;1.3-DiMethyl u;SYM-DIMETHYLUREA;1,3-dimethyl-ure;1,3-DIMETHYLUREA;N,N'-DIMETHYLUREA;n,n'-dimethyl-ure;Dimethylcarbamide; Dimethylurea (DMU; Uses; 1,3-Dimethylurea; DIMETHYL UREA; DIMETYLURE; dimethylürea; dımethyl urea; dimetil üre; dimethyl ürea; dımethyl ure; dimtil ürea; DIMETHYL UREA; dimetily ürea; dimetil üre; DIMETİL ÜRE; DIMETHYL UREA; DIMETYL URE; DIMETHYL REA; dimethyl üre; dimetyl ürea; dimethyl üre; dımethyl urea; (CH3NH)2CO;AKOS B029718;1.3-DiMethyl u;SYM-DIMETHYLUREA;1,3-dimethyl-ure;1,3-DIMETHYLUREA;N,N'-DIMETHYLUREA;n,n'-dimethyl-ure;Dimethylcarbamide; Dimethylurea (DMU; Uses; 1,3-Dimethylurea; DIMETHYL UREA; DIMETYLURE; dimethylürea; dımethyl urea; dimetil üre; dimethyl ürea; dımethyl ure; dimtil ürea; DIMETHYL UREA; dimetily ürea; dimetil üre; DIMETİL ÜRE; DIMETHYL UREA; DIMETYL URE; DIMETHYL REA; dimethyl üre; dimetyl ürea; dimethyl üre; dımethyl urea; (CH3NH)2CO;AKOS B029718;1.3-DiMethyl u;SYM-DIMETHYLUREA;1,3-dimethyl-ure;1,3-DIMETHYLUREA;N,N'-DIMETHYLUREA;n,n'-dimethyl-ure;Dimethylcarbamide; Dimethylurea (DMU; Uses; 1,3-Dimethylurea; DIMETHYL UREA; DIMETYLURE; dimethylürea; dımethyl urea; dimetil üre; dimethyl ürea; dımethyl ure; dimtil ürea; DIMETHYL UREA; dimetily ürea; dimetil üre; DIMETİL ÜRE; DIMETHYL UREA; DIMETYL URE; DIMETHYL REA; dimethyl üre; dimetyl ürea; dimethyl üre; dımethyl urea; (CH3NH)2CO;AKOS B029718;1.3-DiMethyl u;SYM-DIMETHYLUREA;1,3-dimethyl-ure;1,3-DIMETHYLUREA;N,N'-DIMETHYLUREA;n,n'-dimethyl-ure;Dimethylcarbamide; Dimethylurea (DMU; Uses; 1,3-Dimethylurea; DIMETHYL UREA; DIMETYLURE; dimethylürea; dımethyl urea; dimetil üre; dimethyl ürea; dımethyl ure; dimtil ürea; DIMETHYL UREA; dimetily ürea; dimetil üre; DIMETİL ÜRE; DIMETHYL UREA; DIMETYL URE; DIMETHYL REA; dimethyl üre; dimetyl ürea; dimethyl üre; dımethyl urea; (CH3NH)2CO;AKOS B029718;1.3-DiMethyl u;SYM-DIMETHYLUREA;1,3-dimethyl-ure;1,3-DIMETHYLUREA;N,N'-DIMETHYLUREA;n,n'-dimethyl-ure;Dimethylcarbamide; Dimethylurea (DMU; Uses; 1,3-Dimethylurea; DIMETHYL UREA; DIMETYLURE; dimethylürea; dımethyl urea; dimetil üre; dimethyl ürea; dımethyl ure; dimtil ürea; DIMETHYL UREA; dimetily ürea; dimetil üre; DIMETİL ÜRE; DIMETHYL UREA; DIMETYL URE; DIMETHYL REA; dimethyl üre; dimetyl ürea; dimethyl üre; dımethyl urea; (CH3NH)2CO;AKOS B029718;1.3-DiMethyl u;SYM-DIMETHYLUREA;1,3-dimethyl-ure;1,3-DIMETHYLUREA;N,N'-DIMETHYLUREA;n,n'-dimethyl-ure;Dimethylcarbamide; Dimethylurea (DMU; Uses; 1,3-Dimethylurea; DIMETHYL UREA; DIMETYLURE; dimethylürea; dımethyl urea; dimetil üre; dimethyl ürea; dımethyl ure; dimtil ürea; DIMETHYL UREA; dimetily ürea; dimetil üre; DIMETİL ÜRE; DIMETHYL UREA; DIMETYL URE; DIMETHYL REA; dimethyl üre; dimetyl ürea; dimethyl üre; dımethyl urea; (CH3NH)2CO;AKOS B029718;1.3-DiMethyl u;SYM-DIMETHYLUREA;1,3-dimethyl-ure;1,3-DIMETHYLUREA;N,N'-DIMETHYLUREA;n,n'-dimethyl-ure;Dimethylcarbamide; Dimethylurea (DMU; Uses; 1,3-Dimethylurea; DIMETHYL UREA; DIMETYLURE; dimethylürea; dımethyl urea; dimetil üre; dimethyl ürea; dımethyl ure; dimtil ürea; DIMETHYL UREA; dimetily ürea; dimetil üre; DIMETİL ÜRE; DIMETHYL UREA; DIMETYL URE; DIMETHYL REA; dimethyl üre; dimetyl ürea; dimethyl üre; dımethyl urea; (CH3NH)2CO;AKOS B029718;1.3-DiMethyl u;SYM-DIMETHYLUREA;1,3-dimethyl-ure;1,3-DIMETHYLUREA;N,N'-DIMETHYLUREA;n,n'-dimethyl-ure;Dimethylcarbamide; Dimethylurea (DMU; Uses; 1,3-Dimethylurea; DIMETHYL UREA; DIMETYLURE; dimethylürea; dımethyl urea; dimetil üre; dimethyl ürea; dımethyl ure; dimtil ürea; DIMETHYL UREA; dimetily ürea; dimetil üre; 1,1-Diméthylurée; DIMETİL ÜRE; DIMETHYL UREA; Urea, N,N-dimethyl; DIMETYL URE; DIMETHYL REA; dimethyl üre; dimetyl ürea; dimethyl üre; dımethyl urea; (CH3NH)2CO;AKOS B029718;1.3-DiMethyl u;SYM-DIMETHYLUREA;1,3-dimethyl-ure;1,3-DIMETHYLUREA;N,N'-DIMETHYLUREA;n,n'-dimethyl-ure;Dimethylcarbamide; Dimethylurea (DMU; Uses; 1,3-Dimethylurea; DIMETHYL UREA; DIMETYLURE; dimethylürea; dımethyl urea; dimetil üre; dimethyl ürea; dımethyl ure; dimtil ürea; DIMETHYL UREA; dimetily ürea; dimetil üre; DIMETİL ÜRE; DIMETHYL UREA; DIMETYL URE; DIMETHYL REA; dimethyl üre; dimetyl ürea; dimethyl üre; dımethyl urea; (CH3NH)2CO;AKOS B029718;1.3-DiMethyl u;SYM-DIMETHYLUREA;1,3-dimethyl-ure;1,3-DIMETHYLUREA;N,N'-DIMETHYLUREA;n,n'-dimethyl-ure;Dimethylcarbamide; Dimethylurea (DMU; Uses; 1,3-Dimethylurea; DIMETHYL UREA; DIMETYLURE; dimethylürea; dımethyl urea; dimetil üre; dimethyl ürea; dımethyl ure; dimtil ürea; DIMETHYL UREA; dimetily ürea; dimetil üre; DIMETİL ÜRE; DIMETHYL UREA; DIMETYL URE; DIMETHYL REA; dimethyl üre; dimetyl ürea; dimethyl üre; dımethyl urea; (CH3NH)2CO;AKOS B029718;1.3-DiMethyl u;SYM-DIMETHYLUREA;1,3-dimethyl-ure;1,3-DIMETHYLUREA;N,N'-DIMETHYLUREA;n,n'-dimethyl-ure;Dimethylcarbamide; Dimethylurea (DMU; Uses; 1,3-Dimethylurea; DIMETHYL UREA; DIMETYLURE; dimethylürea; dımethyl urea; dimetil üre; dimethyl ürea; dımethyl ure; dimtil ürea; DIMETHYL UREA; dimetily ürea; dimetil üre; DIMETİL ÜRE; DIMETHYL UREA; DIMETYL URE; DIMETHYL REA; dimethyl üre; dimetyl ürea; dimethyl üre; dımethyl urea; (CH3NH)2CO;AKOS B029718;1.3-DiMethyl u;SYM-DIMETHYLUREA;1,3-dimethyl-ure;1,3-DIMETHYLUREA;N,N'-DIMETHYLUREA;n,n'-dimethyl-ure;Dimethylcarbamide; Dimethylurea (DMU; Uses; 1,3-Dimethylurea; DIMETHYL UREA; DIMETYLURE; dimethylürea; dımethyl urea; dimetil üre; dimethyl ürea; dımethyl ure; dimtil ürea; DIMETHYL UREA; dimetily ürea; dimetil üre; DIMETİL ÜRE; DIMETHYL UREA; DIMETYL URE; DIMETHYL REA; dimethyl üre; dimetyl ürea; dimethyl üre; dımethyl urea; (CH3NH)2CO;AKOS B029718;1.3-DiMethyl u;SYM-DIMETHYLUREA;1,3-dimethyl-ure;1,3-DIMETHYLUREA;N,N'-DIMETHYLUREA;n,n'-dimethyl-ure;Dimethylcarbamide; Dimethylurea (DMU; Uses; 1,3-Dimethylurea; DIMETHYL UREA; DIMETYLURE; dimethylürea; dımethyl urea; dimetil üre; dimethyl ürea; dımethyl ure; dimtil ürea; DIMETHYL UREA; dimetily ürea; dimetil üre; DIMETİL ÜRE; DIMETHYL UREA; DIMETYL URE; DIMETHYL REA; dimethyl üre; dimetyl ürea; dimethyl üre; dımethyl urea; (CH3NH)2CO;AKOS B029718;1.3-DiMethyl u;SYM-DIMETHYLUREA;1,3-dimethyl-ure;1,3-DIMETHYLUREA;N,N'-DIMETHYLUREA;n,n'-dimethyl-ure;Dimethylcarbamide; Dimethylurea (DMU; Uses; 1,3-Dimethylurea; DIMETHYL UREA; DIMETYLURE; dimethylürea; dımethyl urea; dimetil üre; dimethyl ürea; dımethyl ure; dimtil ürea; DIMETHYL UREA; dimetily ürea; dimetil üre; DIMETİL ÜRE; DIMETHYL UREA; DIMETYL URE; DIMETHYL REA; dimethyl üre; dimetyl ürea; dimethyl üre; dımethyl urea; (CH3NH)2CO;AKOS B029718;1.3-DiMethyl u;SYM-DIMETHYLUREA;1,3-dimethyl-ure;1,3-DIMETHYLUREA;N,N'-DIMETHYLUREA;n,n'-dimethyl-ure;Dimethylcarbamide; Dimethylurea (DMU; Uses; 1,3-Dimethylurea; DIMETHYL UREA; DIMETYLURE; dimethylürea;

CAS NUMBER:15827-60-8
EC NUMBER:206-896-8

Dimetilüre bir üre türevidir ve organik sentezde bir ara madde olarak kullanılır. Toksisitesi az olan renksiz bir kristal tozdur.Çay yaprağı ve kafeinin sentezi için bir ara madde olarak ve ayrıca elyaf işleme maddelerinin üretimi için kullanılır.
Formül: C3H8N2O
Kaynama noktası: 269,1 °C
Molar kütle: 88,108 g/mol
Yoğunluk: 1,14 g/cm³

Dimethylurea (DMU) (IUPAC systematic name: 1,3-Dimethylurea ) is a urea derivative and used as an intermediate in organic synthesis. It is a colorless crystalline powder with little toxicity. 1,3-Dimethylurea is used for synthesis of caffeine, theophylline, pharmachemicals, textile aids, herbicides and others.[2] In the textile processing industry 1,3-dimethylurea is used as intermediate for the production of formaldehyde-free easy-care finishing agents for textiles. The estimated world production of DMU is estimated to be less than 25,000 tons. N,N′-Dimethylurea (1,3-Dimethylurea), an alkyl urea derivative,[3] is a nonlinear organic material.[4] It forms needle-shaped crystals. It has been crystallized by using ethylacetate (solvent) and heptane (precipitant) by vapor diffusion technique. Its crystals has one molecule in each asymmetric unit. Molecules in crystal are linked by hydrogen bonds. Dimethylurea is the suitable reagent used to investigate the polar structure of its crystals.[1] It may be used in the Dowex-50W ion exchange resin-promoted solvent-free synthesis of N,N′-disubstituted-4-aryl-3,4-dihydropyrimidinones. Tandem Mass Spectrometry data independently generated by Scripps Center for Metabolomics is available to view or download in PDF. 40410.pdf Tested metabolites are featured on Scripps Center for Metabolomics METLIN Metabolite Database. To learn more, visit.-Dimethylurea (1,3-Dimethylurea), an alkyl urea derivative,[3] is a nonlinear organic material.[4] It forms needle-shaped crystals. It has been crystallized by using ethylacetate (solvent) and heptane (precipitant) by vapor diffusion technique. Its crystals has one molecule in each asymmetric unit. Molecules in crystal are linked by hydrogen bonds.


Dimetilüre bir üre türevidir ve organik sentezde bir ara madde olarak kullanılır. Toksisitesi az olan renksiz bir kristal tozdur.Çay yaprağı ve kafeinin sentezi için bir ara madde olarak ve ayrıca elyaf işleme maddelerinin üretimi için kullanılır.
Formül: C3H8N2O
Kaynama noktası: 269,1 °C
Molar kütle: 88,108 g/mol
Yoğunluk: 1,14 g/cm³

Dimethylurea (DMU) (IUPAC systematic name: 1,3-Dimethylurea ) is a urea derivative and used as an intermediate in organic synthesis. It is a colorless crystalline powder with little toxicity. 1,3-Dimethylurea is used for synthesis of caffeine, theophylline, pharmachemicals, textile aids, herbicides and others.[2] In the textile processing industry 1,3-dimethylurea is used as intermediate for the production of formaldehyde-free easy-care finishing agents for textiles. The estimated world production of DMU is estimated to be less than 25,000 tons. N,N′-Dimethylurea (1,3-Dimethylurea), an alkyl urea derivative,[3] is a nonlinear organic material.[4] It forms needle-shaped crystals. It has been crystallized by using ethylacetate (solvent) and heptane (precipitant) by vapor diffusion technique. Its crystals has one molecule in each asymmetric unit. Molecules in crystal are linked by hydrogen bonds. Dimethylurea is the suitable reagent used to investigate the polar structure of its crystals.[1] It may be used in the Dowex-50W ion exchange resin-promoted solvent-free synthesis of N,N′-disubstituted-4-aryl-3,4-dihydropyrimidinones. Tandem Mass Spectrometry data independently generated by Scripps Center for Metabolomics is available to view or download in PDF. 40410.pdf Tested metabolites are featured on Scripps Center for Metabolomics METLIN Metabolite Database. To learn more, visit.-Dimethylurea (1,3-Dimethylurea), an alkyl urea derivative,[3] is a nonlinear organic material.[4] It forms needle-shaped crystals. It has been crystallized by using ethylacetate (solvent) and heptane (precipitant) by vapor diffusion technique. Its crystals has one molecule in each asymmetric unit. Molecules in crystal are linked by hydrogen bonds.


Dimetilüre bir üre türevidir ve organik sentezde bir ara madde olarak kullanılır. Toksisitesi az olan renksiz bir kristal tozdur.Çay yaprağı ve kafeinin sentezi için bir ara madde olarak ve ayrıca elyaf işleme maddelerinin üretimi için kullanılır.
Formül: C3H8N2O
Kaynama noktası: 269,1 °C
Molar kütle: 88,108 g/mol
Yoğunluk: 1,14 g/cm³

Dimethylurea (DMU) (IUPAC systematic name: 1,3-Dimethylurea ) is a urea derivative and used as an intermediate in organic synthesis. It is a colorless crystalline powder with little toxicity. 1,3-Dimethylurea is used for synthesis of caffeine, theophylline, pharmachemicals, textile aids, herbicides and others.[2] In the textile processing industry 1,3-dimethylurea is used as intermediate for the production of formaldehyde-free easy-care finishing agents for textiles. The estimated world production of DMU is estimated to be less than 25,000 tons. N,N′-Dimethylurea (1,3-Dimethylurea), an alkyl urea derivative,[3] is a nonlinear organic material.[4] It forms needle-shaped crystals. It has been crystallized by using ethylacetate (solvent) and heptane (precipitant) by vapor diffusion technique. Its crystals has one molecule in each asymmetric unit. Molecules in crystal are linked by hydrogen bonds. Dimethylurea is the suitable reagent used to investigate the polar structure of its crystals.[1] It may be used in the Dowex-50W ion exchange resin-promoted solvent-free synthesis of N,N′-disubstituted-4-aryl-3,4-dihydropyrimidinones. Tandem Mass Spectrometry data independently generated by Scripps Center for Metabolomics is available to view or download in PDF. 40410.pdf Tested metabolites are featured on Scripps Center for Metabolomics METLIN Metabolite Database. To learn more, visit.-Dimethylurea (1,3-Dimethylurea), an alkyl urea derivative,[3] is a nonlinear organic material.[4] It forms needle-shaped crystals. It has been crystallized by using ethylacetate (solvent) and heptane (precipitant) by vapor diffusion technique. Its crystals has one molecule in each asymmetric unit. Molecules in crystal are linked by hydrogen bonds.

 




 


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