TEDA (CAS 280-57-9) — formula C6H12N2, molecular weight 112.17; category organic chemicals.
| CAS Number | 280-57-9 |
|---|---|
| Molecular Formula | C6H12N2 |
| Molecular Weight | 112.17 |
| Melting Point | 158 °C |
| Boiling Point | 174 °C |
| LogP | -0.2 |
| Applications | Uses: Used as curing agent for urethane foams, used as a singlet oxygen trap and a radioiodine trap, [HSDB], Plastic Composites Manufacturing [Category: Industry], Catalyst in making urethane foams, The only important industrial use of triethylenediamine is as a hardener for polyurethane foams., Anti-fade reagent that scavenges free-radicals produced by excitation of fluorochromes. Added to the mounting medium in fluorescence microscopy to retard photobleaching of fluorescein and other fluorescent dyes.[Sigma-Aldrich, D2522 Sigma 1, 4-Diazabicyclo, Singlet oxygen trap used as diagnostic for singlet oxygen, trap for radioiodine, ... Oxidation and polymerization catalyst, chemical intermediate (metal complexes, quaternary ammonium compounds, etc), bromide and iodine addition compounds., Industry Uses: Absorbent, Filler, Catalyst, Intermediate, Consumer Uses: Catalyst, Methods of Manufacturing: KRAUSE ET AL, BRITISH PATENT 871, 754 (1958 TO HOUDRY PROCESS)., Triethylenediamine can be produced from ethylenediamine or ethanolamine, diethanolamine, or diethylenetriamine with a variety of different catalysts., U.S. Production: 2023: 1, 000, 000 - <2, 500, 000 lb, 2022: 1, 2021: 1, 2020: 850, 000 - <1, This chemical is listed as a High Production Volume (HPV) (65FR81686). Chemicals listed as HPV were produced in or imported into the U.S. in >1 million pounds in 1990 and, or 1994. The HPV list is based on the 1990 Inventory Update Rule. (IUR) (40 CFR part 710 subpart B, 51FR21438)., Production volumes for non-confidential chemicals reported under the Inventory Update Rule. [Table#5434], General Manufacturing Information: Transportation Equipment Manufacturing, Oil and Gas Drilling, Extraction, and Support activities, Utilities, All Other Basic Organic Chemical Manufacturing, All Other Chemical Product and Preparation Manufacturing, Construction, 1, 4-Diazabicyclo[2.2.2]octane: ACTIVE, Triethylenediamine is used to impregnate the activated carbon found in respiratory protection against chemical weapon agents., Certain low-molecular chemical weapon agents such as hydrogen cyanide and cyanogen chloride are poorly absorbed by active carbon. In order to improve protection against these substances, the carbon is impregnated with metallic salts of copper, chromium and sometimes silver. Further impregnation with organic substances also occurs, the most common additive being triethylenediamine. |
| Category | Organic Chemicals |
Documented applications: Uses: Used as curing agent for urethane foams, used as a singlet oxygen trap and a radioiodine trap, [HSDB], Plastic Composites Manufacturing [Category: Industry], Catalyst in making urethane foams, The only important industrial use of triethylenediamine is as a hardener for polyurethane foams., Anti-fade reagent that scavenges free-radicals produced by excitation of fluorochromes. Added to the mounting medium in fluorescence microscopy to retard photobleaching of fluorescein and other fluorescent dyes.[Sigma-Aldrich, D2522 Sigma 1, 4-Diazabicyclo, Singlet oxygen trap used as diagnostic for singlet oxygen, trap for radioiodine, ... Oxidation and polymerization catalyst, chemical intermediate (metal complexes, quaternary ammonium compounds, etc), bromide and iodine addition compounds., Industry Uses: Absorbent, Filler, Catalyst, Intermediate, Consumer Uses: Catalyst, Methods of Manufacturing: KRAUSE ET AL, BRITISH PATENT 871, 754 (1958 TO HOUDRY PROCESS)., Triethylenediamine can be produced from ethylenediamine or ethanolamine, diethanolamine, or diethylenetriamine with a variety of different catalysts., U.S. Production: 2023: 1, 000, 000 - <2, 500, 000 lb, 2022: 1, 2021: 1, 2020: 850, 000 - <1, This chemical is listed as a High Production Volume (HPV) (65FR81686). Chemicals listed as HPV were produced in or imported into the U.S. in >1 million pounds in 1990 and, or 1994. The HPV list is based on the 1990 Inventory Update Rule. (IUR) (40 CFR part 710 subpart B, 51FR21438)., Production volumes for non-confidential chemicals reported under the Inventory Update Rule. [Table#5434], General Manufacturing Information: Transportation Equipment Manufacturing, Oil and Gas Drilling, Extraction, and Support activities, Utilities, All Other Basic Organic Chemical Manufacturing, All Other Chemical Product and Preparation Manufacturing, Construction, 1, 4-Diazabicyclo[2.2.2]octane: ACTIVE, Triethylenediamine is used to impregnate the activated carbon found in respiratory protection against chemical weapon agents., Certain low-molecular chemical weapon agents such as hydrogen cyanide and cyanogen chloride are poorly absorbed by active carbon. In order to improve protection against these substances, the carbon is impregnated with metallic salts of copper, chromium and sometimes silver. Further impregnation with organic substances also occurs, the most common additive being triethylenediamine..
TEDA is a carbon-based organic compound with CAS registry number 280-57-9 and molecular formula C6H12N2 (molecular weight 112.17), belonging to the organic chemicals segment of chemical raw materials.
CAS number: 280-57-9
Its molecular formula C6H12N2 comprises 6 C, 12 H, 2 N atoms.
Also known as: TEDA · 泰达 · 1,4-Diazabicyclo[2.2.2]octane
Category: organic chemicals
The CAS registry number of TEDA is 280-57-9.
Molecular formula C6H12N2, molecular weight 112.17.
It is also registered under: TEDA, 泰达, 1,4-Diazabicyclo[2.2.2]octane.
Recorded applications: Uses: Used as curing agent for urethane foams, used as a singlet oxygen trap and a radioiodine trap, [HSDB], Plastic Composites Manufacturing [Category: Industry], Catalyst in making urethane foams, The only important industrial use of triethylenediamine is as a hardener for polyurethane foams., Anti-fade reagent that scavenges free-radicals produced by excitation of fluorochromes. Added to the mounting medium in fluorescence microscopy to retard photobleaching of fluorescein and other fluorescent dyes.[Sigma-Aldrich, D2522 Sigma 1, 4-Diazabicyclo, Singlet oxygen trap used as diagnostic for singlet oxygen, trap for radioiodine, ... Oxidation and polymerization catalyst, chemical intermediate (metal complexes, quaternary ammonium compounds, etc), bromide and iodine addition compounds., Industry Uses: Absorbent, Filler, Catalyst, Intermediate, Consumer Uses: Catalyst, Methods of Manufacturing: KRAUSE ET AL, BRITISH PATENT 871, 754 (1958 TO HOUDRY PROCESS)., Triethylenediamine can be produced from ethylenediamine or ethanolamine, diethanolamine, or diethylenetriamine with a variety of different catalysts., U.S. Production: 2023: 1, 000, 000 - <2, 500, 000 lb, 2022: 1, 2021: 1, 2020: 850, 000 - <1, This chemical is listed as a High Production Volume (HPV) (65FR81686). Chemicals listed as HPV were produced in or imported into the U.S. in >1 million pounds in 1990 and, or 1994. The HPV list is based on the 1990 Inventory Update Rule. (IUR) (40 CFR part 710 subpart B, 51FR21438)., Production volumes for non-confidential chemicals reported under the Inventory Update Rule. [Table#5434], General Manufacturing Information: Transportation Equipment Manufacturing, Oil and Gas Drilling, Extraction, and Support activities, Utilities, All Other Basic Organic Chemical Manufacturing, All Other Chemical Product and Preparation Manufacturing, Construction, 1, 4-Diazabicyclo[2.2.2]octane: ACTIVE, Triethylenediamine is used to impregnate the activated carbon found in respiratory protection against chemical weapon agents., Certain low-molecular chemical weapon agents such as hydrogen cyanide and cyanogen chloride are poorly absorbed by active carbon. In order to improve protection against these substances, the carbon is impregnated with metallic salts of copper, chromium and sometimes silver. Further impregnation with organic substances also occurs, the most common additive being triethylenediamine..
Category: Organic Chemicals.
Independent reference data for TEDA (CAS 280-57-9), compiled from public chemistry databases.
| CAS Registry Number | 280-57-9 |
|---|---|
| PubChem CID | 9237 |
| Molecular formula | C6H12N2 |
| IUPAC name | 1,4-diazabicyclo[2.2.2]octane |
| UNII (FDA) | X8M57R0JS5 |
| Molecular Weight | 112.17 |
|---|---|
| XLogP3 | -0.2 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 0 |
| Exact Mass | 112.100048391 |
| Monoisotopic Mass | 112.100048391 |
| Topological Polar Surface Area | 6.5 |
| Heavy Atom Count | 8 |
| Boiling Point | 174 °C |
|---|---|
| Boiling Point | 174 °C @760 [mm Hg] |
| Melting Point | 158 °C |
| Flash Point | 62 °C |
| Solubility | 45 g/100 g water at 25 °C |
| Vapor Pressure | 0.74 [mmHg] |
| Dissociation Constants | pKa1 = 3.0; pKa2 = 8.7 |
1,4-Diazabicyclo[2.2.2]octane; Triethylenediamine; 280-57-9; Dabco; 1,4-DIAZABICYCLO(2.2.2)OCTANE; Dabco 33LV; Dabco crystal; 1,4-Ethylenepiperazine; TEDA; Texacat TD 100; Dabco EG; N,N'-endo-Ethylenepiperazine; 1,4-Diazabicyclo-octane; D 33LV; Thancat TD 33; DTXSID0022016
| GHS notification summary | 0.7% (6 / 801) |
|---|
| GHS notification summary | 0.7% (6 / 801) |
|---|---|
| Reported hazard statements | H228 (82.6%), H302 (96.5%), H315 (97.3%), H318 (50.7%), H319 (44.2%), H335 (16.4%), H412 (14.5%), H361 |
This chemical does not meet GHS hazard criteria for 0.7% (6 of 801) of reports.
H228 (82.6%): Flammable solid [Danger Flammable solids]
1,4-Diazabicyclo[2.2.2]octane · CAS 280-57-9 · C6H12N2. UNII X8M57R0JS5. Boiling Point: 174 °C; Boiling Point: 174 °C @760 [mm Hg]; Melting Point: 158 °C.
Source: PubChem / Wikidata; the batch COA governs where values differ.
Supplier: Jinan Shenghe Chemical Co., Ltd.
中文页面: 泰达