107-45-9 Suppliers

Recommended suppliersmore

Product
FOB Price
Min.Order
Supply Ability
Supplier
Contact Supplier

Factory Supply 1,1,3,3-tetramethylbutylamine
Cas No: 107-45-9
No Data
1
1
Ality Chemical Corporation
Contact Supplier

1,1,3,3-Tetramethylbutylamine
Cas No: 107-45-9
USD $ 2.0-2.0 / Kilogram
1 Kilogram
1-10 Metric Ton/Month
Dayang Chem (Hangzhou) Co.,Ltd.
Contact Supplier

1,1,3,3-Tetramethylbutylamine
Cas No: 107-45-9
USD $ 1.2-5.0 / Kiloliter
5 Kiloliter
3000 Metric Ton/Month
Chemwill Asia Co., Ltd.
Contact Supplier

tert-OctylaMine
Cas No: 107-45-9
USD $ 1100.0-1500.0 / Metric Ton
5 Metric Ton
10 Metric Ton/Month
Hebei yanxi chemical co.,LTD.
Contact Supplier

1,1,3,3-Tetramethylbutylamine CAS NO.107-45-9
Cas No: 107-45-9
No Data
10 Gram
500 Kilogram/Month
Changchun Artel lmport and Export trade company
Contact Supplier

tert-Octylamine
Cas No: 107-45-9
No Data
1 Kilogram
1 Metric Ton/Month
HANGZHOU YUNUO CHEMICAL CO.,LTD
Contact Supplier

tert-Octylamine
Cas No: 107-45-9
No Data
No Data
No Data
Hangzhou Keyingchem Co.,Ltd
Contact Supplier

tert-Octylamine
Cas No: 107-45-9
No Data
No Data
5
Hangzhou J&H Chemical Co., Ltd.
Contact Supplier

tert-OctylaMine
Cas No: 107-45-9
USD $ 100.0-100.0 / Gram
10 Gram
500 Kilogram/Month
Zibo Hangyu Biotechnology Development Co., Ltd
Contact Supplier

tert-OctylaMine
Cas No: 107-45-9
No Data
1 Kilogram
1 Metric Ton/Day
Zibo Dorne chemical technology co. LTD
Contact Supplier

107-45-9 Usage

Chemical Properties

CLEAR LIQUID

Check Digit Verification of cas no

The CAS Registry Mumber 107-45-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,0 and 7 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 107-45:
(5*1)+(4*0)+(3*7)+(2*4)+(1*5)=39
39 % 10 = 9
So 107-45-9 is a valid CAS Registry Number.

InChI:InChI=1/C8H19N/c1-7(2,3)6-8(4,5)9/h6,9H2,1-5H3/p+1

107-45-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name	tert-Octylamine

1.2 Other means of identification

Product number	-
Other names	Tert-Octylamine

1.3 Recommended use of the chemical and restrictions on use

Identified uses	For industry use only. Functional fluids (open systems)
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:107-45-9 SDS

107-45-9Synthetic route

: 263254-99-5
3-Methyl-3-tert-octylamino-1-butyne

A: 107-45-9
tert-Octylamine

B: 263255-00-1
tert-Octyl-tert-pentylamine

Conditions

Conditions	Yield
With hydrogen; palladium on activated charcoal In various solvent(s) under 2947.74 Torr; Hydrogenolysis; Catalytic hydrogenation;	A 60% B 35%

: 5342-78-9
2,2,4-trimethyl-4-nitro-pentane

: 107-45-9
tert-Octylamine

Conditions

Conditions	Yield
With nickel Hydrogenation;
With hydrogenchloride; tin

: 6111-88-2
2-chloro-2,4,4-trimethylpentane

: 3315-16-0
silver cyanate

: 107-45-9
tert-Octylamine

Conditions

Conditions	Yield
Kochen des Reaktionsprodukts mit 40prozentig.KOH;

: 6111-88-2
2-chloro-2,4,4-trimethylpentane

: 107-45-9
tert-Octylamine

Conditions

Conditions	Yield
With diethyl ether; magnesium anschliessend mit Chloramin;

: 10151-02-7
N-(2,4,4-trimethylpentan-2-yl)formamide

: 107-45-9
tert-Octylamine

Conditions

Conditions	Yield
With sodium hydroxide

: 3302-12-3
2,2,4,4-tetramethylpentanoic acid

: 107-45-9
tert-Octylamine

Conditions

Conditions	Yield
With thionyl chloride Umsetzung des erhaltenen Saeurechlorids mit NaN3 in siedendem Toluol und anschliessendes Kochen mit 40prozentig.KOH;

: 5459-42-7
N-1,1'3,3'-tetramethylbutylacetamide

: 107-45-9
tert-Octylamine

Conditions

Conditions	Yield
With potassium hydroxide; ethylene glycol

: 107-39-1
2,4,4-trimethyl-1-pentene

: 506-77-4
cyanogen chloride

: 107-45-9
tert-Octylamine

Conditions

Conditions	Yield
With sulfuric acid anschliessend mit Wasser;

: 6111-88-2
2-chloro-2,4,4-trimethylpentane

A: 107-45-9
tert-Octylamine

B: 75-64-9
tert-butylamine

Conditions

Conditions	Yield
With aluminium trichloride; nitrogen trichloride In dichloromethane

: 107-39-1
2,4,4-trimethyl-1-pentene

: 107-45-9
tert-Octylamine

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1: concentrated H2SO4; glacial acetic acid 2: KOH; ethylene glycol View Scheme
Multi-step reaction with 2 steps 1: concentrated H2SO4; glacial acetic acid 2: aq. NaOH solution View Scheme
Multi-step reaction with 2 steps 1: hydrogen chloride / unter Kuehlung mit Eis 2: Kochen des Reaktionsprodukts mit 40prozentig.KOH View Scheme
Multi-step reaction with 2 steps 2: NCl3, AlCl3 / CH2Cl2 View Scheme

: 14542-93-9
1,1,3,3-tetramethylbutane isonitrile

: 107-45-9
tert-Octylamine

Conditions

Conditions	Yield
Stage #1: 1,1,3,3-tetramethylbutane isonitrile In methanol; dichloromethane at 20℃; Stage #2: With N-ethyl-N,N-diisopropylamine In dichloromethane at 20℃; for 2h;

: 107-45-9
tert-Octylamine

: 123-38-6
propionaldehyde

: 2,4,4-trimethyl-N-propylidene-2-pentanamine

Conditions

Conditions	Yield
With sodium sulfate In dichloromethane at 10 - 20℃;	100%

: 823792-22-9
7-phenylacetamido-3-(4-methylthiazol-5-yl)vinyl-3-cephem-4-carboxylic acid

: C21H19N3O4S2

: 107-45-9
tert-Octylamine

A: C8H19N*C21H19N3O4S2

B: C8H19N*C21H19N3O4S2

Conditions

Conditions	Yield
In water; acetone at 5℃; for 3h;	A 99.3% B n/a

: 115-20-8
1,1,1-trichloroethanol

: 107-45-9
tert-Octylamine

: 24424-99-5
di-tert-butyl dicarbonate

: (1,1,3,3-Tetramethyl-butyl)-carbamic acid 2,2,2-trichloro-ethyl ester

Conditions

Conditions	Yield
With dmap In acetonitrile at 82℃; for 34h;	99%

: 626-60-8
3-Chloropyridine

: 107-45-9
tert-Octylamine

: N-(2,4,4-trimethylpentan-2-yl)pyridin-3-amine

Conditions

Conditions	Yield
With chloro(η3-2-cinnam-1-yl)(1,3-(diisopropylphenyl)-4-(diisopropylamino)imidazol-2-ylidene)palladium(II); potassium tert-butylate In 1,2-dimethoxyethane at 60℃; for 4h; Buchwald-Hartwig Coupling; Schlenk technique; Glovebox; Sealed tube; Inert atmosphere;	99%
With C26H33N2P; C39H46N3O3PPdS; sodium t-butanolate In 1,4-dioxane at 100℃; for 24h; Inert atmosphere;	73%

: 110-62-3
pentanal

: 107-45-9
tert-Octylamine

: 595-91-5
triphenylacetic acid

: (R)-1-oxo-1-((2,4,4-trimethylpentan-2-yl)amino)hexan-2-yl 2,2,2-triphenylacetate

Conditions

Conditions	Yield
Stage #1: pentanal; triphenylacetic acid With (R)-3,3'-bis(9-anthracenyl)-1,1'-binaphthyl-2,2'-diyl hydrogenphosphate; magnesium sulfate In chloroform at -20℃; for 0.166667h; Passerini Condensation; Schlenk technique; Inert atmosphere; Stage #2: tert-Octylamine In chloroform at -20℃; for 36h; Passerini Condensation; Inert atmosphere; Schlenk technique; enantioselective reaction;	99%

: 495-76-1
piperonol

: 107-45-9
tert-Octylamine

: 1137195-75-5
(E)-N-(benzo[d][1,3]dioxol-5-ylmethylene)-2,4,4-trimethylpentan-2-amine

Conditions

Conditions	Yield
With palladium on aluminium oxyhydroxide; oxygen at 90℃; under 760.051 Torr; for 24h;	98%

: 107-45-9
tert-Octylamine

: 830-79-5
2,4,6-trimethoxybenzaldehyde

: 1-(2,4,6-trimethoxyphenyl)-N-(2,4,4-trimethylpentan-2-yl)methanimine

Conditions

Conditions	Yield
In benzene Reflux; Dean-Stark;	98%

: 107-45-9
tert-Octylamine

: 24424-99-5
di-tert-butyl dicarbonate

: 1611-57-0
1,1,3,3-tetramethylbutyl isocyanate

Conditions

Conditions	Yield
With dmap In dichloromethane at 25℃; for 0.166667h;	97%

: 107-45-9
tert-Octylamine

: 24424-99-5
di-tert-butyl dicarbonate

: 107-18-6
allyl alcohol

A: 100247-48-1
allyl N-1,1,3,3-tetramethylbutylcarbamate

B: 2092-58-2
N,N'-bis(1,1,3,3-tetramethylbutyl)urea

Conditions

Conditions	Yield
With dmap In acetonitrile at 82℃; for 34h;	A 97% B n/a

: 107-45-9
tert-Octylamine

: 124-63-0
methanesulfonyl chloride

: 899252-59-6
N-(1,1,3,3-tetramethyl-butyl)-methanesulfonamide

Conditions

Conditions	Yield
With triethylamine In dichloromethane at 0 - 20℃; for 1.75h;	97%

: 107-45-9
tert-Octylamine

: N-sulfinyl-tert-octylamine

Conditions

Conditions	Yield
With thionyl chloride; triethylamine In diethyl ether at 0℃; for 2h; Inert atmosphere;	97%
With thionyl chloride; Triphenylmethylamin In diethyl ether at 0℃; for 2h; Inert atmosphere;	30%

: 107-45-9
tert-Octylamine

: 24424-99-5
di-tert-butyl dicarbonate

: 100-51-6
benzyl alcohol

A: 2092-58-2
N,N'-bis(1,1,3,3-tetramethylbutyl)urea

B: (1,1,3,3-Tetramethyl-butyl)-carbamic acid benzyl ester

Conditions

Conditions	Yield
With dmap In acetonitrile for 17h; Heating;	A n/a B 96%

: 866431-82-5
4-(acetylamino)-5-amino-7-tert-butyl-N,N-diisopropyl-9-oxo-9H-xanthene-2-carboxamide

: 75-44-5
phosgene

: 107-45-9
tert-Octylamine

: 4-(acetylamino)-7-tert-butyl-N,N-diisopropyl-9-oxo-5-({[(1,1,3,3-tetramethylbutyl)amino]carbonyl}amino)-9H-xanthene-2-carboxamide

Conditions

Conditions	Yield
Stage #1: 4-(acetylamino)-5-amino-7-tert-butyl-N,N-diisopropyl-9-oxo-9H-xanthene-2-carboxamide; phosgene In dichloromethane; toluene for 0.333333h; Heating; Stage #2: tert-Octylamine In toluene	96%

: 107-45-9
tert-Octylamine

: 7721-01-9
tantalum pentachloride

: 2H3NC(CH3)2CH2C(CH3)3(1+)*Ta(NC(CH3)2CH2C(CH3)3)Cl5(2-)=[H3NC(CH3)2CH2C(CH3)3]2[Ta(NC(CH3)2CH2C(CH3)3)Cl5]

Conditions

Conditions	Yield
In diethyl ether; toluene N2-atmosphere; 3 equiv. amine, stirring for 4 h; evapn. (vac.), washing (pentane), drying (vac.);	96%

: 108-31-6
maleic anhydride

: 107-45-9
tert-Octylamine

: 131365-14-5
N-[(1,1,3,3-tetramethyl)butyl]maleamic acid

Conditions

Conditions	Yield
In toluene at 45 - 50℃; for 1h;	95%
In toluene at 45 - 50℃; for 2h;

: 75-44-5
phosgene

: 107-45-9
tert-Octylamine

: 168705-30-4
8-Amino-6-tert-butyl-4-oxo-4H-chromene-2-carboxylic acid butylamide

: 6-tert-Butyl-4-oxo-8-[3-(1,1,3,3-tetramethyl-butyl)-ureido]-4H-chromene-2-carboxylic acid butylamide

Conditions

Conditions	Yield
	95%

: 866431-85-8
butyl 4-amino-7-tert-butyl-5-nitro-9-oxo-9H-xanthene-2-carboxylate

: 75-44-5
phosgene

: 107-45-9
tert-Octylamine

: 866431-86-9
butyl 7-tert-butyl-5-nitro-9-oxo-4-({[(1,1,3,3-tetramethylbutyl)amino]carbonyl}amino)-9H-xanthene-2-carboxylate

Conditions

Conditions	Yield
Stage #1: butyl 4-amino-7-tert-butyl-5-nitro-9-oxo-9H-xanthene-2-carboxylate; phosgene In dichloromethane; toluene Stage #2: tert-Octylamine In toluene	95%

: 107-45-9
tert-Octylamine

: 866-55-7
dichlorodiethylstannane

: 121043-81-0
1,3-bis(2,4,4-trimethyl-2-pentyl)-2,2,4,4-tetraethyl-1,3,2,4-diazadistannetidine

Conditions

Conditions	Yield
With n-butyllithium In hexane exclusion of oxygen and moisture; refluxing (3 h) of tert-octylamine and n-BuLi, cooling (-78°C), addn. of Et2SnCl2, warming to room temp., refluxing (2 h); filtn., volatiles removal (room temp., vac.);	95%

: 107-45-9
tert-Octylamine

: 100-52-7
benzaldehyde

: 3598-75-2
benzyl-(1,1,3,3-tetramethyl-butyl)-amine

Conditions

Conditions	Yield
Stage #1: tert-Octylamine; benzaldehyde With titanium(IV) isopropylate In tetrahydrofuran at 20℃; for 1h; Inert atmosphere; Stage #2: With ammonia borane In tetrahydrofuran at 20℃; for 7h; Inert atmosphere;	95%

: 131543-46-9
Glyoxal

: 107-45-9
tert-Octylamine

: 56376-10-4
N,N'-bis(1,1,3,3-tetramethylbutyl)-1,4-diaza-1,3-butadiene

Conditions

Conditions	Yield
In water at 20℃; for 1h;	95%
In water at 20℃; for 1h;	95%
In water at 20℃; for 1h;	95%

: 107-45-9
tert-Octylamine

: 1620-98-0
3,5-di-t-butyl-4-hydroxybenzaldehyde

: 1151854-56-6
2,6-di-tert-butyl-4-((2,4,4-trimethylpentan-2-ylimino)methyl)phenol

Conditions

Conditions	Yield
In toluene at 60 - 110℃; for 2h;	94.48%
In toluene at 60 - 110℃; Azeotropic removal of water; Inert atmosphere;	94.48%

: 107-45-9
tert-Octylamine

: 31044-98-1
2,2,4-tetramethyl-4-nitrosopentane

Conditions

Conditions	Yield
With peracetic acid In water; ethyl acetate at 0℃; for 2h;	94%
With sodium tungstate (VI) dihydrate; dihydrogen peroxide; ethylene diamine tetraacetic acid tetrasodium salt In methanol; water at 15℃; for 21h;	52%
Multi-step reaction with 3 steps 1: aq. K2CO3 / various solvent(s) / 5 h / 50 °C 2: aq. N2H4 / methanol / 75 h / 20 °C 3: aq. MeOBr / methanol / -78 - -20 °C View Scheme

: 866431-78-9
4-amino-7-tert-butyl-N,N-diisopropyl-5-nitro-9-oxo-9H-xanthene-2-carboxamide

: 75-44-5
phosgene

: 107-45-9
tert-Octylamine

: 866431-79-0
7-tert-butyl-N,N-diisopropyl-5-nitro-9-oxo-4-({[(1,1,3,3-tetramethylbutyl)amino]carbonyl}amino)-9H-xanthene-2-carboxamide

Conditions

Conditions	Yield
Stage #1: 4-amino-7-tert-butyl-N,N-diisopropyl-5-nitro-9-oxo-9H-xanthene-2-carboxamide; phosgene In dichloromethane; toluene for 0.333333h; Heating; Stage #2: tert-Octylamine In toluene at 20℃;	94%

: 1121-60-4
pyridine-2-carbaldehyde

: 107-45-9
tert-Octylamine

: 1392472-53-5
(E)-2,4,4-trimethyl-N-(pyridin-2-ylmethylene)pentan-2-amine

Conditions

Conditions	Yield
In dichloromethane for 1.5h; Inert atmosphere; Reflux; Dean-Stark;	94%

: 14508-49-7
2-chloropyrazin

: 107-45-9
tert-Octylamine

: N-(2,4,4-trimethylpentan-2-yl)pyrazin-2-amine

Conditions

Conditions	Yield
With C47H70BrO4PPdSi; sodium t-butanolate In tetrahydrofuran at 20℃; for 1h; Schlenk technique; Inert atmosphere; Sealed tube;	94%
With C41H42N3O3PPdS; sodium t-butanolate In 1,4-dioxane at 120℃; for 12h; Inert atmosphere;	50%

: 107-45-9
tert-Octylamine

: 766-51-8
2-Chloroanisole

: 2-methoxy-N-tert-octylaniline

Conditions

Conditions	Yield
With chloro(η3-2-cinnam-1-yl)(1,3-(diisopropylphenyl)-4-(diisopropylamino)imidazol-2-ylidene)palladium(II); potassium tert-butylate In 1,2-dimethoxyethane at 60℃; for 4h; Buchwald-Hartwig Coupling; Schlenk technique; Glovebox; Sealed tube; Inert atmosphere;	94%

: 107-45-9
tert-Octylamine

: 2200-85-3
5-bromo-3-chloro-2-hydroxybenzoic acid

: 5-bromo-3-chloro-2-hydroxy-N-(2,4,4-trimethylpentan-2-yl)benzamide

Conditions

Conditions	Yield
Stage #1: 5-bromo-3-chloro-2-hydroxybenzoic acid With O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; N-ethyl-N,N-diisopropylamine In N,N-dimethyl-formamide for 0.166667h; Stage #2: tert-Octylamine In N,N-dimethyl-d6-formamide at 20℃;	94%
Stage #1: 5-bromo-3-chloro-2-hydroxybenzoic acid With N-ethyl-N,N-diisopropylamine In N,N-dimethyl-formamide for 0.166667h; Stage #2: tert-Octylamine In N,N-dimethyl-formamide at 20℃;	94%

: 107-45-9
tert-Octylamine

: 98-68-0
4-methoxy-phenyl-sulphonyl chloride

: 4-methoxy-N-(2,4,4-trimethylpentan-2-yl)benzenesulfonamide

Conditions

Conditions	Yield
With triethylamine In dichloromethane at 20℃; for 12h;	94%

: 131543-46-9
Glyoxal

: 107-45-9
tert-Octylamine

: 56376-10-4
glyoxal-bis-(1,1,3,3-tetramethyl-butylimine)

Conditions

Conditions	Yield
In water at 20℃; for 4h;	93%
In water at 20℃; for 4h;	93%
With formic acid In hexane for 3h; Ambient temperature;
With water

: 107-45-9
tert-Octylamine

: 24424-95-1
di-tert-butyl tricarbonate

: 1611-57-0
1,1,3,3-tetramethylbutyl isocyanate

Conditions

Conditions	Yield
In dichloromethane for 0.0833333h; Ambient temperature;	93%

107-45-9Upstream product

107-45-9Downstream Products

107-45-9Related news

Synthesis and characterization of three-layered zinc phosphites containing tert-Octylamine (cas 107-45-9) molecules with template and ligand roles08/18/2019

Three-layered zinc phosphites containing single monoamine molecules with different roles have been synthesized using hydro(solvo)thermal methods and characterized by single-crystal X-ray diffraction, thermogravimetric analysis, and infrared spectroscopy. Compound 1, (C8H17NH3)4Zn3(HPO3)5·3H2O, ...detailed

107-45-9Relevant articles and documents

-

Smolin

, p. 295,296 (1955)

Di-tert-alkyl nitroxyl radicals. Synthesis, physical properties and applications as inhibitors of vinyl polmerization at elevated temperatures

Sosnovsky, George,Jawdosiuk, Mikolaj,Clumpner, J. Michael

, p. 109 - 126 (2007/10/03)

Stable di-tert-alkylnitroxyl radicals, tert-butyl-tert-pentylnitroxyl (4a), di-tert-pentylnitroxyl (4b) and tert-octyl-tert-pentylnitroxyl (4c), the homologs of di-tert-butylnitroxyl (1), were synthesized from tert-alkyl amines 7a-c via the 3-tert-alkylamino-3-methyl-1-butynes 8a-c. Oxidation of 8a,b with hydrogen peroxide lead to relatively unstable N-tert-alkyl-N-(1,1-dimethyl-prop-2-ynyl)nitroxyl radicals 15a,b. The thermal stability, vapor pressure data, ultraviolet, visible and electron paramagnetic resonance spectra of 4a-c were recorded. The radicals were explored as potential inhibitors of unwanted alkene polymerization reactions at elevated temperatures, in comparison with the aliphatic di-tert-butyl nitroxyl (1), the alicyclic nitroxyl radicals 2,2,6,6-tetramethylpiperidin-1-oxyl (2) and 4-hydroxy-2,2,6,6-tetramethyl-piperidin-1-oxyl (3), some commercial polymerization inhibitors, such as diethyl-hydroxylamine (Pennstop, 16), ammonium salt of N-hydroxy-N-nitrosobenzenamine (Cupferron, 17), bis(2,2,6,6-tetramethyl-4-piperidyl) sebacate (Tinuvin 770, 18), and the well-known spin traps 2-methyl-2-nitrosopropane (19) and tert-butylhydroxylamine (20).

Catalysts for alkoxylation reactions

-

, (2008/06/13)

Catalysts producing a sharply peaked alkoxylation distribution during the alkoxylation of organic materials comprise mixtures of BF3 and metal alkyls or metal alkoxides, SiF4 and metal alkyls or metal alkoxides, or mixtures of these catalysts.

Post a RFQ

Cas No.:

Product Name:

Quantity:

Email:

Company name:

Valid Period:

Detailed Requirements:

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)

What can I do for you?
Get Best Price

Get Best Price for 107-45-9

CAS

107-45-9

107-45-9

Basic information

Chemical Properties

Safety Data

107-45-9 Suppliers

Recommended suppliersmore

107-45-9 Usage

Chemical Properties

Check Digit Verification of cas no

107-45-9SDS

SAFETY DATA SHEETS

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

1.Identification

1.1 GHS Product identifier

1.2 Other means of identification

1.3 Recommended use of the chemical and restrictions on use

1.4 Supplier's details

1.5 Emergency phone number

107-45-9Synthetic route

107-45-9Upstream product

107-45-9Downstream Products

107-45-9Related news

107-45-9Relevant articles and documents

-

Smolin

, p. 295,296 (1955)

Di-tert-alkyl nitroxyl radicals. Synthesis, physical properties and applications as inhibitors of vinyl polmerization at elevated temperatures

Sosnovsky, George,Jawdosiuk, Mikolaj,Clumpner, J. Michael

, p. 109 - 126 (2007/10/03)

Catalysts for alkoxylation reactions

-

, (2008/06/13)