Welcome to LookChem.com Sign In|Join Free

CAS

  • or

996-35-0

Post Buying Request

996-35-0 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

996-35-0 Usage

Chemical Properties

colourless liquid

General Description

N,N-Dimethylisopropylamine may be used as an alkylating agent in the preparation of N-methylaniline via palladium catalyzed N-methylation of aniline under microwave condition. It may also be used to prepare a hypergolic ionic liquid by reacting with hydrazoic acid.

Flammability and Explosibility

Highlyflammable

Check Digit Verification of cas no

The CAS Registry Mumber 996-35-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,9 and 6 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 996-35:
(5*9)+(4*9)+(3*6)+(2*3)+(1*5)=110
110 % 10 = 0
So 996-35-0 is a valid CAS Registry Number.
InChI:InChI=1/C5H13N/c1-5(2)6(3)4/h5H,1-4H3

996-35-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name N,N-Dimethylisopropylamine

1.2 Other means of identification

Product number -
Other names N,N-dimethylpropan-2-amine

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Adhesives and sealant chemicals,Agricultural chemicals (non-pesticidal),Intermediates,Process regulators
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:996-35-0 SDS

996-35-0Synthetic route

dimethyl amine
124-40-3

dimethyl amine

acetone
67-64-1

acetone

N,N-dimethylisopropyl amine
996-35-0

N,N-dimethylisopropyl amine

Conditions
ConditionsYield
With hydrogen; ZrO2-containing catalyst at 80 - 170℃; under 150015 Torr;99%
With water; hydrogen; platinum at 25℃; under 2280 Torr; Ueberdruck;
methyl magnesium iodide
917-64-6

methyl magnesium iodide

α-(dimethylamino)-propionitrile
5350-67-4

α-(dimethylamino)-propionitrile

A

N,N-dimethylisopropyl amine
996-35-0

N,N-dimethylisopropyl amine

B

3-(dimethylamino)-2-butanone
10524-60-4

3-(dimethylamino)-2-butanone

Conditions
ConditionsYield
With diethyl ether
reagiert analog mit Aethylmagnesiumbromid; mit Propylmagnesiumbromid und mit Cyclohexylmagnesiumchlorid nur die entspr.Ketone erhalten werden;
formaldehyd
50-00-0

formaldehyd

isopropylamine hydrochloride
15572-56-2

isopropylamine hydrochloride

N,N-dimethylisopropyl amine
996-35-0

N,N-dimethylisopropyl amine

Conditions
ConditionsYield
at 135℃;
N,N,N-Trimethylisopropylammonium iodide
4995-18-0

N,N,N-Trimethylisopropylammonium iodide

ethanolamine
141-43-5

ethanolamine

A

N,N-dimethylisopropyl amine
996-35-0

N,N-dimethylisopropyl amine

B

trimethylamine
75-50-3

trimethylamine

Conditions
ConditionsYield
at 154℃; Rate constant;
formaldehyd
50-00-0

formaldehyd

isopropylamine
75-31-0

isopropylamine

N,N-dimethylisopropyl amine
996-35-0

N,N-dimethylisopropyl amine

Conditions
ConditionsYield
With formic acid; water
With formic acid
With formic acid
methyl magnesium iodide
917-64-6

methyl magnesium iodide

N1,N1-dimethyl-N2-phenylformamidine
1783-25-1

N1,N1-dimethyl-N2-phenylformamidine

N,N-dimethylisopropyl amine
996-35-0

N,N-dimethylisopropyl amine

Conditions
ConditionsYield
(i) AcCl, (ii) /BRN= 1209226/; Multistep reaction;
propene
187737-37-7

propene

N,N,N,N,-tetramethylethylenediamine
110-18-9

N,N,N,N,-tetramethylethylenediamine

N,N-dimethylisopropyl amine
996-35-0

N,N-dimethylisopropyl amine

Conditions
ConditionsYield
With ethyllithium at 150℃;
1,3,5-Triisopropyl-1,3,5-triazacyclohexane
10556-98-6

1,3,5-Triisopropyl-1,3,5-triazacyclohexane

mono-trimethylsilylphosphite
91076-68-5

mono-trimethylsilylphosphite

A

N,N-dimethylisopropyl amine
996-35-0

N,N-dimethylisopropyl amine

B

N-methylpropan-2-amine
4747-21-1

N-methylpropan-2-amine

2-(tert-Butylazo)-2(dimethylamino)propane
126191-35-3

2-(tert-Butylazo)-2(dimethylamino)propane

A

N,N-dimethylisopropyl amine
996-35-0

N,N-dimethylisopropyl amine

B

Isobutane
75-28-5

Isobutane

C

Acetone N,N-dimethylenamine
22499-75-8

Acetone N,N-dimethylenamine

D

2-Dimethylamino-4-methyl-pentadien-(1,3)
22752-64-3

2-Dimethylamino-4-methyl-pentadien-(1,3)

E

dimethyl amine
124-40-3

dimethyl amine

F

acetone
67-64-1

acetone

Conditions
ConditionsYield
In benzene-d6 Mechanism; Product distribution; Heating;
2-(tert-Butylazo)-2(dimethylamino)propane
126191-35-3

2-(tert-Butylazo)-2(dimethylamino)propane

A

N,N-dimethylisopropyl amine
996-35-0

N,N-dimethylisopropyl amine

B

Isobutane
75-28-5

Isobutane

C

acetone tert-butylhydrazone
33050-99-6

acetone tert-butylhydrazone

D

1,2-di-tert-butylhydrazine
13952-69-7

1,2-di-tert-butylhydrazine

E

dimethyl amine
124-40-3

dimethyl amine

F

acetone
67-64-1

acetone

Conditions
ConditionsYield
In [D3]acetonitrile Mechanism; Product distribution; Heating; solvent wet or dried;
2-(tert-Butylazo)-2(dimethylamino)propane
126191-35-3

2-(tert-Butylazo)-2(dimethylamino)propane

A

N,N-dimethylisopropyl amine
996-35-0

N,N-dimethylisopropyl amine

B

Isobutane
75-28-5

Isobutane

C

dimethyl-(1,1,2,2-tetramethyl-propyl)-amine
3733-36-6

dimethyl-(1,1,2,2-tetramethyl-propyl)-amine

D

dimethyl amine
124-40-3

dimethyl amine

E

acetone
67-64-1

acetone

F

isobutene
115-11-7

isobutene

Conditions
ConditionsYield
In benzene-d6 Mechanism; Product distribution; Irradiation; other solvent (wet CD3CN);
2-(tert-Butylazo)-2(dimethylamino)propane
126191-35-3

2-(tert-Butylazo)-2(dimethylamino)propane

A

N,N-dimethylisopropyl amine
996-35-0

N,N-dimethylisopropyl amine

B

Isobutane
75-28-5

Isobutane

C

dimethyl-(1,1,2,2-tetramethyl-propyl)-amine
3733-36-6

dimethyl-(1,1,2,2-tetramethyl-propyl)-amine

D

acetone tert-butylhydrazone
33050-99-6

acetone tert-butylhydrazone

E

dimethyl amine
124-40-3

dimethyl amine

F

isobutene
115-11-7

isobutene

Conditions
ConditionsYield
In sodium hydroxide; d(4)-methanol Mechanism; Product distribution; Heating; or CH3OD / NaOH;
2-(tert-Butylazo)-2(dimethylamino)propane
126191-35-3

2-(tert-Butylazo)-2(dimethylamino)propane

A

N,N-dimethylisopropyl amine
996-35-0

N,N-dimethylisopropyl amine

B

acetone tert-butylhydrazone
33050-99-6

acetone tert-butylhydrazone

C

1,2-di-tert-butylhydrazine
13952-69-7

1,2-di-tert-butylhydrazine

D

dimethyl amine
124-40-3

dimethyl amine

E

isobutene
115-11-7

isobutene

Conditions
ConditionsYield
In d(4)-methanol Mechanism; Product distribution; Irradiation; other solvents;
N'-Eth-(E)-ylidene-N-isopropyl-N,N-dimethyl-hydrazinium; iodide

N'-Eth-(E)-ylidene-N-isopropyl-N,N-dimethyl-hydrazinium; iodide

N,N-dimethylisopropyl amine
996-35-0

N,N-dimethylisopropyl amine

Conditions
ConditionsYield
With potassium hydroxide In methanol for 0.5h; Heating; Yield given;
dimethyl amine
124-40-3

dimethyl amine

acetone
67-64-1

acetone

platinum

platinum

N,N-dimethylisopropyl amine
996-35-0

N,N-dimethylisopropyl amine

Conditions
ConditionsYield
under 2280 Torr; Hydrogenation;
diethyl ether
60-29-7

diethyl ether

2-dimethylamino-2-methylpropionitrile
2273-40-7

2-dimethylamino-2-methylpropionitrile

sodium

sodium

N,N-dimethylisopropyl amine
996-35-0

N,N-dimethylisopropyl amine

FeC10H9CH2N(CH3)2CH(CH3)2(1+)*Br(1-)={FeC10H9CH2N(CH3)2CH(CH3)2}Br

FeC10H9CH2N(CH3)2CH(CH3)2(1+)*Br(1-)={FeC10H9CH2N(CH3)2CH(CH3)2}Br

A

(Fe(C5H5)(C5H4CH2))2N(CH3)2(1+)

(Fe(C5H5)(C5H4CH2))2N(CH3)2(1+)

B

N,N-dimethylisopropyl amine
996-35-0

N,N-dimethylisopropyl amine

Conditions
ConditionsYield
In not given
In not given
N,N-dimethylthioformamide
758-16-7

N,N-dimethylthioformamide

methylmagnesium bromide
75-16-1

methylmagnesium bromide

N,N-dimethylisopropyl amine
996-35-0

N,N-dimethylisopropyl amine

Conditions
ConditionsYield
In tetrahydrofuran; 1,2-dichloro-ethane at 20℃; Inert atmosphere; Reflux;
formaldehyd
50-00-0

formaldehyd

formic acid
64-18-6

formic acid

isopropylamine
75-31-0

isopropylamine

N,N-dimethylisopropyl amine
996-35-0

N,N-dimethylisopropyl amine

Conditions
ConditionsYield
Eschweiler-Clark Amine Methylation;
(E)-1,2-diphenyl-ethene
103-30-0

(E)-1,2-diphenyl-ethene

N,N-dimethylisopropyl amine
996-35-0

N,N-dimethylisopropyl amine

(2,3-Diphenyl-propyl)-isopropyl-methyl-amine
76233-40-4

(2,3-Diphenyl-propyl)-isopropyl-methyl-amine

Conditions
ConditionsYield
Irradiation;95%
1-fluoro-1,1-bis(phenylsulfonyl)methane
910650-82-7

1-fluoro-1,1-bis(phenylsulfonyl)methane

N,N-dimethylisopropyl amine
996-35-0

N,N-dimethylisopropyl amine

N-(2-fluoro-2,2-bis(phenylsulfonyl)ethyl)-N-methylpropan-2-amine
1438847-91-6

N-(2-fluoro-2,2-bis(phenylsulfonyl)ethyl)-N-methylpropan-2-amine

Conditions
ConditionsYield
Stage #1: N,N-dimethylisopropyl amine With di-isopropyl azodicarboxylate at 0 - 20℃; for 1h; Schlenk technique;
Stage #2: 1-fluoro-1,1-bis(phenylsulfonyl)methane In N,N-dimethyl-formamide at 50℃; for 3h; regioselective reaction;
95%
N,N-dimethylisopropyl amine
996-35-0

N,N-dimethylisopropyl amine

N,N-dimethylisopropylammonium azide
1218938-71-6

N,N-dimethylisopropylammonium azide

Conditions
ConditionsYield
With hydrogen azide In diethyl ether at 0 - 10℃; for 6h;92%
N,N-dimethylisopropyl amine
996-35-0

N,N-dimethylisopropyl amine

2-(benzenesulfonyl)-6-chlorobenzothiazole

2-(benzenesulfonyl)-6-chlorobenzothiazole

C12H15ClN2S

C12H15ClN2S

Conditions
ConditionsYield
With di-tert-butoxydiazene In methanol at 50℃; for 8h;91%
2-chloropyrimidine
1722-12-9

2-chloropyrimidine

N,N-dimethylisopropyl amine
996-35-0

N,N-dimethylisopropyl amine

A

2-(dimethylamino)pyrimidine
5621-02-3

2-(dimethylamino)pyrimidine

B

Isopropyl-methyl-pyrimidin-2-yl-amine
141193-17-1

Isopropyl-methyl-pyrimidin-2-yl-amine

Conditions
ConditionsYield
In tetrahydrofuran at 100℃; under 6000480 Torr; for 96h;A 6%
B 90%
N,N-dimethylisopropyl amine
996-35-0

N,N-dimethylisopropyl amine

2-(benzenesulfonyl)-5-phenyloxazole
1245771-19-0

2-(benzenesulfonyl)-5-phenyloxazole

C14H18N2O

C14H18N2O

Conditions
ConditionsYield
With di-tert-butoxydiazene In methanol at 50℃; for 8h;90%
1-(benzenesulfonyl)isoquinoline
27302-34-7

1-(benzenesulfonyl)isoquinoline

N,N-dimethylisopropyl amine
996-35-0

N,N-dimethylisopropyl amine

C14H18N2

C14H18N2

Conditions
ConditionsYield
With sodium dihydrogenphosphate; di-tert-butoxydiazene In methanol at 50℃; for 24h;90%
N,N-dimethylisopropyl amine
996-35-0

N,N-dimethylisopropyl amine

2-(benzenesulfonyl)-4-(ethoxycarbonyl)thiazole

2-(benzenesulfonyl)-4-(ethoxycarbonyl)thiazole

C11H18N2O2S

C11H18N2O2S

Conditions
ConditionsYield
With di-tert-butoxydiazene In ethanol at 50℃; for 8h;89%
N,N-dimethylisopropyl amine
996-35-0

N,N-dimethylisopropyl amine

4-(phenylsulfonyl)benzonitrile
28525-13-5

4-(phenylsulfonyl)benzonitrile

[(4-cyanophenyl)methyl](methyl)(isopropyl)amine
928649-05-2

[(4-cyanophenyl)methyl](methyl)(isopropyl)amine

Conditions
ConditionsYield
With sodium dihydrogenphosphate; di-tert-butoxydiazene In methanol at 50℃; for 24h; Reagent/catalyst;88%
2-phenylsulphonyl-1,3-thiazole
71274-57-2

2-phenylsulphonyl-1,3-thiazole

N,N-dimethylisopropyl amine
996-35-0

N,N-dimethylisopropyl amine

isopropyl(methyl)(2-thiazolylmethyl)amine

isopropyl(methyl)(2-thiazolylmethyl)amine

Conditions
ConditionsYield
With di-tert-butoxydiazene In methanol at 50℃; for 8h;87%
N,N-dimethylisopropyl amine
996-35-0

N,N-dimethylisopropyl amine

2-(benzenesulfonyl)-6-methoxybenzothiazole

2-(benzenesulfonyl)-6-methoxybenzothiazole

isopropyl[2-(6-methoxybenzothiazolyl)methyl](methyl)amine

isopropyl[2-(6-methoxybenzothiazolyl)methyl](methyl)amine

Conditions
ConditionsYield
With di-tert-butoxydiazene In methanol at 50℃; for 8h;87%
N,N-dimethylisopropyl amine
996-35-0

N,N-dimethylisopropyl amine

2-(benzenesulfonyl)-1-methylbenzimidazole

2-(benzenesulfonyl)-1-methylbenzimidazole

C13H19N3

C13H19N3

Conditions
ConditionsYield
With di-tert-butoxydiazene In methanol at 50℃; for 8h;85%
N,N-dimethylisopropyl amine
996-35-0

N,N-dimethylisopropyl amine

methyl 4-(benzenesulfonyl)benzoate
38337-00-7

methyl 4-(benzenesulfonyl)benzoate

isopropyl[4-(methoxycarbonyl)phenylmethyl](methyl)-amine

isopropyl[4-(methoxycarbonyl)phenylmethyl](methyl)-amine

Conditions
ConditionsYield
With sodium dihydrogenphosphate; di-tert-butoxydiazene In methanol at 50℃; for 24h;83%
3,6-dichlorpyridazine
141-30-0

3,6-dichlorpyridazine

N,N-dimethylisopropyl amine
996-35-0

N,N-dimethylisopropyl amine

A

6-chloro-N,N-dimethyl-pyridazin-3-amine
7145-60-0

6-chloro-N,N-dimethyl-pyridazin-3-amine

B

(6-Chloro-pyridazin-3-yl)-isopropyl-methyl-amine
141193-19-3

(6-Chloro-pyridazin-3-yl)-isopropyl-methyl-amine

Conditions
ConditionsYield
In tetrahydrofuran at 100℃; under 6000480 Torr; for 96h;A 6%
B 82%
N,N-dimethylisopropyl amine
996-35-0

N,N-dimethylisopropyl amine

N-Benzylidenebenzylamine N-oxide
3376-26-9

N-Benzylidenebenzylamine N-oxide

C19H26N2O

C19H26N2O

Conditions
ConditionsYield
With 4,4'-Dichlorobenzophenone In acetone at 20℃; for 1h; Solvent; Wavelength; Reagent/catalyst; UV-irradiation; Inert atmosphere; regioselective reaction;82%
1-iodo-butane
542-69-8

1-iodo-butane

N,N-dimethylisopropyl amine
996-35-0

N,N-dimethylisopropyl amine

butyldimethylisopropylammonium iodide

butyldimethylisopropylammonium iodide

Conditions
ConditionsYield
In butanone for 3h; Menshutkin reaction; Heating;81%
N,N-dimethylisopropyl amine
996-35-0

N,N-dimethylisopropyl amine

dichloromethane
75-09-2

dichloromethane

phosphonic acid diethyl ester
762-04-9

phosphonic acid diethyl ester

diethyl (N-isopropylmethylaminomethyl)phosphonate

diethyl (N-isopropylmethylaminomethyl)phosphonate

Conditions
ConditionsYield
In N,N-dimethyl-formamide at 100℃; for 12h; Schlenk technique; Inert atmosphere; Sealed tube;80%
2-chlorobenzo[d][1,3]thiazole
615-20-3

2-chlorobenzo[d][1,3]thiazole

N,N-dimethylisopropyl amine
996-35-0

N,N-dimethylisopropyl amine

A

2-dimethylaminobenzothiazole
4074-74-2

2-dimethylaminobenzothiazole

B

Benzothiazol-2-yl-isopropyl-methyl-amine
136540-11-9

Benzothiazol-2-yl-isopropyl-methyl-amine

Conditions
ConditionsYield
In tetrahydrofuran at 100℃; under 6000480 Torr; for 96h;A 20%
B 79%
N,N-dimethylisopropyl amine
996-35-0

N,N-dimethylisopropyl amine

p-Xylylene dichloride
623-25-6

p-Xylylene dichloride

4-(chloromethyl)-N-isopropyl-N,N-dimethylbenzenemethan-aminium chloride
419532-61-9

4-(chloromethyl)-N-isopropyl-N,N-dimethylbenzenemethan-aminium chloride

Conditions
ConditionsYield
In tetrahydrofuran79%
N,N-dimethylisopropyl amine
996-35-0

N,N-dimethylisopropyl amine

ethyl iodide
75-03-6

ethyl iodide

ethyldimethylisopropylammonium iodide
105198-03-6

ethyldimethylisopropylammonium iodide

Conditions
ConditionsYield
In butanone for 0.75h; Menshutkin reaction; Heating;77%
N,N-dimethylisopropyl amine
996-35-0

N,N-dimethylisopropyl amine

1-iodine-1H,1H,2H,2H,3H,3H-perfluoroheptane
183547-74-2

1-iodine-1H,1H,2H,2H,3H,3H-perfluoroheptane

C12H19F9N(1+)*I(1-)

C12H19F9N(1+)*I(1-)

Conditions
ConditionsYield
In acetonitrile at 150℃; for 24h; Schlenk technique;76%
N,N-dimethylisopropyl amine
996-35-0

N,N-dimethylisopropyl amine

2-(benzenesulfonyl)-4-phenylthiazole

2-(benzenesulfonyl)-4-phenylthiazole

C14H18N2S

C14H18N2S

Conditions
ConditionsYield
With di-tert-butoxydiazene In methanol at 50℃; for 8h;76%
N,N-dimethylisopropyl amine
996-35-0

N,N-dimethylisopropyl amine

1-ethynyl-4-(n-pentyl)benzene
79887-10-8

1-ethynyl-4-(n-pentyl)benzene

C18H27N
1118639-22-7

C18H27N

Conditions
ConditionsYield
Stage #1: N,N-dimethylisopropyl amine With diethylazodicarboxylate at 0 - 20℃; for 1h; Inert atmosphere;
Stage #2: 1-ethynyl-4-(n-pentyl)benzene With copper(l) iodide In tetrahydrofuran at 0 - 20℃; Inert atmosphere; regioselective reaction;
75%
N,N-dimethylisopropyl amine
996-35-0

N,N-dimethylisopropyl amine

C15H12F3NO

C15H12F3NO

C20H25F3N2O

C20H25F3N2O

Conditions
ConditionsYield
With 4,4'-Dichlorobenzophenone In acetone at 20℃; for 1h; Inert atmosphere; UV-irradiation; regioselective reaction;75%
N,N-dimethylisopropyl amine
996-35-0

N,N-dimethylisopropyl amine

2-(benzenesulfonyl)benzimidazole
91822-75-2

2-(benzenesulfonyl)benzimidazole

(2-benzimidazolylmethyl)(isopropyl)(methyl)amine

(2-benzimidazolylmethyl)(isopropyl)(methyl)amine

Conditions
ConditionsYield
With di-tert-butoxydiazene In methanol at 50℃; for 8h;75%
N,N-dimethylisopropyl amine
996-35-0

N,N-dimethylisopropyl amine

C-(2-furyl)-N-benzylnitrone
22661-25-2, 162740-08-1

C-(2-furyl)-N-benzylnitrone

C17H24N2O2

C17H24N2O2

Conditions
ConditionsYield
With 4,4'-Dichlorobenzophenone In acetone at 20℃; for 3.5h; Inert atmosphere; UV-irradiation; regioselective reaction;74%
N,N-dimethylisopropyl amine
996-35-0

N,N-dimethylisopropyl amine

4-Chloro-2,6-bis(trifluoromethyl)pyridine
81269-96-7

4-Chloro-2,6-bis(trifluoromethyl)pyridine

A

(2,6-Bis-trifluoromethyl-pyridin-4-yl)-dimethyl-amine
136540-06-2

(2,6-Bis-trifluoromethyl-pyridin-4-yl)-dimethyl-amine

B

(2,6-Bis-trifluoromethyl-pyridin-4-yl)-isopropyl-methyl-amine
136540-04-0

(2,6-Bis-trifluoromethyl-pyridin-4-yl)-isopropyl-methyl-amine

Conditions
ConditionsYield
In tetrahydrofuran at 100℃; under 6000480 Torr; for 96h;A 13%
B 73%
N,N-dimethylisopropyl amine
996-35-0

N,N-dimethylisopropyl amine

N-benzyl-C-(2-pyridyl) nitrone

N-benzyl-C-(2-pyridyl) nitrone

C18H25N3O

C18H25N3O

Conditions
ConditionsYield
With 4,4'-Dichlorobenzophenone In acetone at 20℃; for 1h; Inert atmosphere; UV-irradiation; regioselective reaction;72%
N,N-dimethylisopropyl amine
996-35-0

N,N-dimethylisopropyl amine

aniline
62-53-3

aniline

N-methylaniline
100-61-8

N-methylaniline

Conditions
ConditionsYield
With palladium 10% on activated carbon In toluene at 175℃; for 1.5h; Inert atmosphere; Microwave irradiation;70%

996-35-0Relevant articles and documents

Supramolecular assembly of borate with quaternary ammonium: Crystal structure and tunable luminescent properties

Liang, Jie,Wang, Yong-Gang,Wang, Ying-Xia,Liao, Fu-Hui,Lin, Jian-Hua

, p. 99 - 104 (2013)

A new borate [C6H16N][B5O 6(OH)4] (1) is synthesized hydrothermally by the reaction of isopropyltrimethylammonium hydroxide with boric acid. It crystallizes in the triclinic space group P-1 with the parameters a=9.1578(10) A, b=9.372(9) A, c=9.9812(10) A, α=66.508(2)°, β=74.751(2)°, γ=81.893(2)°. The [B5O6(OH)4] - anions are interlinked via hydrogen bonding forming a 3D supramolecular network containing large cavities, where reside the (CH 3)3(i-C3H7) N+ cations. This borate shows tunable luminescent properties with temperature, heating-treatment, exciting-light, and solvents. The fluorescent intensity of 1 enhances 6-fold with decreasing the temperature from 25 K to 78 K. By treatment under different temperatures, the luminescence of 1 shifted from blue to white and the sample treated at 230 °C emits bright white light to naked eyes. The hybrid borate can disperse in different solvents, and shows a red-shifted and intense emission in polar solvents.

METHOD FOR THE CONTINUOUS PRODUCTION OF AN AMINE

-

Page/Page column 21, (2008/06/13)

The invention relates to a method for the continuous production of an amine by reacting a primary or secondary alcohol, aldehyde and/or ketone with hydrogen and a nitrogen compound, selected from the group including ammonia, primary and secondary amines, at a temperature in the range of from 80 to 350 °C in the presence of a zirconium dioxide-containing catalyst, the catalytically active weight of the catalyst prior to its reduction with hydrogen containing 90 to 99.8 % by weight of zirconium dioxide (ZrO2), 0.1 to 5.0 % by weight of oxygen-containing compounds of palladium and 0.1 to 5.0 % by weight of oxygen-containing compounds of platinum.

Intramolecular motions in a series of crystalline benzylammonium bromides and dibenzylamines studied by CP/MAS NMR

Riddell, Frank G.,Rogerson, Martin

, p. 493 - 504 (2007/10/03)

A series of 15 compounds including ammonium bromides containing one or two benzyl groups with H, methyl, isopropyl, tert-butyl and tert-amyl substituents and dibenzylamihe with N-isopropyl-, N-tert-butyl- and N-tert-amyl substituents have been synthesised and studied by CP/MAS NMR. The results of dynamic NMR studies on the solids suggest that there is a dramatically wide range of molecular motions occurring in this simple series of compounds: A combination of 2D CPEXSY, dynamic line shape analyses and T1ρ measurements reveals the considerable extent of intramolecular group motions including rotations of methyl, tert-butyl, tert-amyl and phenyl groups. Rates of rotation and activation parameters for these molecular motions are derived where appropriate. In the case of benzyl-tert-butylammonium bromide, where two independent molecules of the compound exist in the asymmetric unit it is shown that the independent processes of tert-butyl rotation in the two molecules have vastly different activation energies that differ by ca. 16 kJ mol-1. The extent of the motions observed suggests that commonly held prejudices about the rigidity of molecules in crystalline solids need revising.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 996-35-0