It is a prime candidate for most applications due to its overall performance and cost effectiveness. Its good thermal stability makes it a candidate for applications in which resistance to high temperature is required. Because of its high bromine con
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inquiryUnique advantages for Decabromodiphenyl oxide Cas 1163-19-5 Guaranteed the purity High quality & competitive price Quality control Fast feedback Prompt shipment Appearance:Powder Storage:2-8°C Package:25kg/bag Application:Flame retardant
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The above product is Ality Chemical's strong item with best price, good quality and fast supply. Ality Chemical has been focusing on the research and production of this field for over 14 years. At the same time, we are always committed to providi
This product is a broad-spectrum and highly effective added flame retardant. It has the characteristics of low dosage, strong flame retardancy and high thermal stability. Appearance:white powder Storage:Store in a cool, dry, well ventilated warehou
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inquiryProduct description: Product name Decabromodiphenyl oxide CAS number 1163-19-5 Assay ≥83% Appearance White powder Capacity 2000mt/year Application Flame retardant for rubber,
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inquiryDecabromodiphenyl oxide Basic information Product Name: Decabromodiphenyl oxide Synonyms: 1,1’-oxybis(2,3,4,5,6-pentabromo-benzen;1,1’-oxybis[2,3,4,5,6-pentabromo-benzen;berk
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inquiryProduct Name: Decabromodiphenyl Oxide (DBDPO /DECA) Advantages: Good FR-efficiency, Low additive, Multi-function Application: HIPS, PE,PP, PBT, PA6, PA66, ABS, Textile Package: 25 Kg kraft bag with plastic lining Appe
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inquiryProduct Name: Decabromodiphenyl oxide CAS: 1163-19-5 MF: C12Br10O MW: 959.17 EINECS: 214-604-9 Decabromodiphenyl oxide Structure Decabromodiphenyl oxide Chemical Properties Melting point >300 °C(lit.) Boiling point 425
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inquiryConditions | Yield |
---|---|
With aluminum tri-bromide; bromine for 3h; Heating; | 98% |
With aluminum tri-bromide; bromine | |
Stage #1: diphenylether With bromine at 25 - 58℃; for 1.66667 - 2.13333h; Stage #2: With bromine; aluminum (III) chloride at 55 - 60℃; for 6.38333 - 6.5h; Product distribution / selectivity; |
diphenylether
bromine
aluminium bromide
2,2',3,3',4,4',5,5',6,6'-Decabromodiphenyl ether
diphenylether
A
2,2',3,3',4,5,5',6,6'-nonabromodiphenyl ether
B
nonabromodiphenyl ether
C
BDE-207
D
2,2',3,3',4,4',5,5',6,6'-Decabromodiphenyl ether
Conditions | Yield |
---|---|
With bromine; aluminum (III) chloride at 55 - 61℃; for 6.25h; Product distribution / selectivity; | A n/a B 0.24 %Chromat. C n/a D 99.54 %Chromat. |
Stage #1: diphenylether With bromine for 0.416667 - 1.41667h; Heating / reflux; Stage #2: With bromine; aluminum (III) chloride at 56.1 - 59℃; for 7.13333 - 9.78333h; Product distribution / selectivity; | A n/a B 0.031 - 0.205 %Chromat. C n/a D 99.90 - 99.95 %Chromat. |
Stage #1: diphenylether With bromine at 40℃; Stage #2: With bromine; aluminum (III) chloride at 56.9 - 60.4℃; for 1.83333 - 1.85h; Product distribution / selectivity; | A n/a B 0.181 - 0.220 %Chromat. C n/a D 99.634 - 99.696 %Chromat. |
diphenylether
A
nonabromodiphenyl ether
B
2,2',3,3',4,4',5,5',6,6'-Decabromodiphenyl ether
Conditions | Yield |
---|---|
Stage #1: diphenylether With bromine at 40℃; Stage #2: With bromine; aluminum (III) chloride at 56.5 - 78.4℃; under 1385.82 - 1458.22 Torr; for 3.65 - 4.36667h; Product distribution / selectivity; | A 0.233 - 0.526 %Chromat. B 99.44 - 99.70 %Chromat. |
diphenylether
A
2,2',3,3',4,5,5',6,6'-nonabromodiphenyl ether
B
BDE-207
C
C12Br9ClO
F
2,2',3,3',4,4',5,5',6,6'-Decabromodiphenyl ether
Conditions | Yield |
---|---|
With bromine; bromine chloride; aluminum (III) chloride at 55 - 57℃; for 2.23333h; Product distribution / selectivity; Heating / reflux; | A n/a B n/a C n/a D n/a E n/a F 97.2 %Chromat. |
diphenylether
A
2,2',3,3',4,5,5',6,6'-nonabromodiphenyl ether
B
nonabromodiphenyl ether
C
BDE-207
D
C12Br9ClO
G
2,2',3,3',4,4',5,5',6,6'-Decabromodiphenyl ether
Conditions | Yield |
---|---|
With bromine; bromine chloride; aluminum (III) chloride at 56℃; for 0.0666667h; Product distribution / selectivity; Heating / reflux; | A n/a B 0.14 %Chromat. C n/a D n/a E n/a F n/a G 99.29 %Chromat. |
Conditions | Yield |
---|---|
With sodium hydroxide; palladium diacetate; triphenylphosphine In isopropyl alcohol at 81.9℃; for 5h; Product distribution; Mechanism; other aromatic mono- and polyhalides, var. solvents, transition metal salt, ligands, temperature, and reaction time; | 92% |
With methanol; gold; hydrogen; caesium carbonate at 100℃; under 3800.26 Torr; for 96h; | 89% |
With cadmium selenide; triethylamine In N,N-dimethyl-formamide at 20℃; for 24h; Irradiation; Sealed tube; | 54% |
With 2 wt.% Pd/TiO2 In tetrahydrofuran; methanol for 1h; Catalytic behavior; Kinetics; Reagent/catalyst; UV-irradiation; Inert atmosphere; Darkness; | 15.7% |
With borane-ammonia complex In water; isopropyl alcohol at 50℃; for 12h; Sealed tube; | 97 %Chromat. |
2,2',3,3',4,4',5,5',6,6'-Decabromodiphenyl ether
A
1,1,2,2-tetrabromoethene
B
pentabromobenzene
C
hexabromobenzene
D
hexabromobenzofuran
Conditions | Yield |
---|---|
thermolysis; Further byproducts given; | A n/a B 0.5% C 5% D 0.1% |
2,2',3,3',4,4',5,5',6,6'-Decabromodiphenyl ether
A
hexabromo-1,3-butadiene
B
pentabromobenzene
C
hexabromobenzene
D
hexabromobenzofuran
Conditions | Yield |
---|---|
thermolysis; Further byproducts given; | A n/a B 0.5% C 5% D 0.1% |
2,2',3,3',4,4',5,5',6,6'-Decabromodiphenyl ether
A
pentabromobenzene
B
hexabromobenzene
C
hexabromobenzofuran
D
octabromostyrene
Conditions | Yield |
---|---|
thermolysis; Further byproducts given; | A 0.5% B 5% C 0.1% D n/a |
2,2',3,3',4,4',5,5',6,6'-Decabromodiphenyl ether
A
1,1,2,2-tetrabromoethene
B
hexabromo-1,3-butadiene
C
pentabromobenzene
D
hexabromobenzene
E
hexabromobenzofuran
F
octabromostyrene
Conditions | Yield |
---|---|
Product distribution; thermolysis; | A n/a B n/a C 0.5% D 5% E 0.1% F n/a G n/a |
2,2',3,3',4,4',5,5',6,6'-Decabromodiphenyl ether
A
2,3,7,8-Tetrabromodibenzofuran
B
2,3,7,8-tetrabromodibenzodioxin
Conditions | Yield |
---|---|
at 400℃; thermolysis; Further byproducts given; | A 4.5 B 4.0 (unit not given) |
at 400℃; thermolysis; Further byproducts given; | A 4.5 (unit not given) B 4.0 |
With antimony(III) trioxide; polybutylene terephtalate at 400℃; Product distribution; thermolysis; similar results with various plastics containing the title compound and other brominated aromatic compounds used as flame retardants(tetrabromobisphenol A, hexabromocyclododecane); | A 4.5 (unit not given) B 4.0 (unit not given) |
2,2',3,3',4,4',5,5',6,6'-Decabromodiphenyl ether
A
2,2',3,3',4,5,5',6,6'-nonabromodiphenyl ether
B
nonabromodiphenyl ether
C
BDE-207
Conditions | Yield |
---|---|
In methanol; water for 1.66667h; Kinetics; Quantum yield; Further Variations:; Solvents; Reagents; UV-irradiation; | |
With 2-oxo-propionic acid; sodium hydroxide In tetrahydrofuran; methanol; water Kinetics; Reagent/catalyst; Photolysis; Inert atmosphere; | |
With 2 wt.% Pd/TiO2 In tetrahydrofuran; methanol Reagent/catalyst; UV-irradiation; Inert atmosphere; Darkness; |
2,2',3,3',4,4',5,5',6,6'-Decabromodiphenyl ether
A
nonabromodiphenyl ether
B
BDE-207
D
2,3,4,6-tetrabromophenyl 2,4,5-tribromophenyl ether
Conditions | Yield |
---|---|
With honey In acetone at 60℃; for 672h; Darkness; |
2,2',3,3',4,4',5,5',6,6'-Decabromodiphenyl ether
B
nonabromodiphenyl ether
Conditions | Yield |
---|---|
With tetrabutylammonium tetrafluoroborate In N,N-dimethyl-formamide Pschor Arylation; Electrochemical reaction; |
Conditions | Yield |
---|---|
With air for 2h; Milling; Green chemistry; |
2,2',3,3',4,4',5,5',6,6'-Decabromodiphenyl ether
Conditions | Yield |
---|---|
With 2 wt.% Pd/TiO2 In tetrahydrofuran; methanol for 0.0333333h; UV-irradiation; Inert atmosphere; Darkness; |
2,2',3,3',4,4',5,5',6,6'-Decabromodiphenyl ether
Conditions | Yield |
---|---|
With titanium(IV) oxide In tetrahydrofuran; methanol for 0.166667h; UV-irradiation; Inert atmosphere; Darkness; |
2,2',3,3',4,4',5,5',6,6'-Decabromodiphenyl ether
Conditions | Yield |
---|---|
With titanium(IV) oxide In tetrahydrofuran; methanol for 1h; UV-irradiation; Inert atmosphere; Darkness; |
Conditions | Yield |
---|---|
With 2 wt.% Pd/TiO2 In tetrahydrofuran; methanol for 0.666667h; Catalytic behavior; Kinetics; Reagent/catalyst; UV-irradiation; Inert atmosphere; Darkness; |
Conditions | Yield |
---|---|
With 2 wt.% Pd/TiO2 In tetrahydrofuran; methanol for 0.166667h; Catalytic behavior; Kinetics; Reagent/catalyst; UV-irradiation; Inert atmosphere; Darkness; |
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