halazone structure
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Common Name | halazone | ||
|---|---|---|---|---|
| CAS Number | 80-13-7 | Molecular Weight | 270.09000 | |
| Density | 1.717 g/cm3 | Boiling Point | 437ºC at 760 mmHg | |
| Molecular Formula | C7H5Cl2NO4S | Melting Point | 213ºC | |
| MSDS | N/A | Flash Point | 218.1ºC | |
Use of halazoneHalazone is an atypical antimicrobial sulfonamide derivative and a carbonic anhydrase II inhibitor with a Kd value of 1.45 µM. Halazone protects sodium channels from inactivation. Halazone is widely used for disinfection of drinking water[1][2]. |
This table lists Chinese names, IUPAC names and various aliases of this chemical substance.
| Name | Halazone |
|---|---|
| Synonym | More Synonyms |
This table contains bioactivity, target information and biological‑assay experimental data of this compound.
| Description | Halazone is an atypical antimicrobial sulfonamide derivative and a carbonic anhydrase II inhibitor with a Kd value of 1.45 µM. Halazone protects sodium channels from inactivation. Halazone is widely used for disinfection of drinking water[1][2]. |
|---|---|
| Related Catalog | |
| In Vitro | Halazone is chemically closely related to Chloramine-T, the nitrogen atom is linked with two instead of one chlorine atom and, certainly more important here, a methyl group is replaced by a carboxyl group. The effect of Halazone on the sodium current is studied in voltage-clamped single nerve fibers of the frog. The oxidant Halazone drastically inhibits inactivation[1]. |
| References |
This table shows physicochemical parameters including melting point, boiling point, density, solubility and optical rotation. Missing data is marked as N/A.
| Density | 1.717 g/cm3 |
|---|---|
| Boiling Point | 437ºC at 760 mmHg |
| Melting Point | 213ºC |
| Molecular Formula | C7H5Cl2NO4S |
| Molecular Weight | 270.09000 |
| Flash Point | 218.1ºC |
| Exact Mass | 268.93200 |
| PSA | 83.06000 |
| LogP | 2.76390 |
| InChIKey | XPDVQPODLRGWPL-UHFFFAOYSA-N |
| SMILES | O=C(O)c1ccc(S(=O)(=O)N(Cl)Cl)cc1 |
| Stability | Stable, but may be light sensitive. Incompatible with strong oxidizing agents. |
This table provides MSDS information including hazard classification, first‑aid, fire‑fighting, spill handling, operation and storage instructions.
This table summarizes toxicological test data, acute & chronic toxicity and ecological hazard parameters for this chemical.
CHEMICAL IDENTIFICATION
HEALTH HAZARD DATAACUTE TOXICITY DATA
MUTATION DATA
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This table covers safety warnings, protective measures, incompatible substances and disposal guidelines for this compound.
| Hazard Codes | T+ |
|---|---|
| RIDADR | 1479 |
| WGK Germany | 3 |
| RTECS | DG8050000 |
| Packaging Group | III |
| Hazard Class | 5.1 |
| HS Code | 2935009090 |
This table presents publicly reported synthetic routes, reaction conditions, reactants and product information of the compound.
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halazone CAS#:80-13-7 |
| Literature: Saljoughian, M.; Sadeghi, M. T. Monatshefte fuer Chemie, 1986 , vol. 117, p. 553 - 556 |
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halazone CAS#:80-13-7 |
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Literature: A Handbook of Antiseptics |
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halazone CAS#:80-13-7
Learn More
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| Literature: DE318899 ; Fortschr. Teerfarbenfabr. Verw. Industriezweige, vol. 13, p. 769 |
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halazone CAS#:80-13-7 |
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Literature: A Handbook of Antiseptics |
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halazone CAS#:80-13-7 |
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Literature: A Handbook of Antiseptics |
This table lists upstream starting materials and downstream derivative products related to this chemical.
| Precursor 4 | |
|---|---|
| DownStream 2 | |
This table shows customs‑related data including HS‑code, tariff and regulatory conditions for import and export.
| HS Code | 2935009090 |
|---|---|
| Summary | 2935009090 other sulphonamides VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:35.0% |
This table contains target information, in‑vitro & in‑vivo assay data for this compound.
This table collects all English aliases, systematic names and CAS‑related synonyms of the compound.
| Pantocide |
| Benzoesaeure-(sulfonsaeure-(4)-dichloramid) |
| Gynamide |
| EINECS 201-253-1 |
| Zeptabs |
| p-Dichlorsulfamid-benzoesaeure |
| Halazon |
| Pantosid |
| Pentocid |
| 4-dichlorosulfamoyl-benzoic acid |
| PANTOCID |
| 4-Dichlorsulfamoyl-benzoesaeure |
| Halozone |
| MFCD00045858 |
| 4-[(dichloroamino)sulfonyl]-benzoic acid |
This section contains frequently‑asked‑questions about this compound, including basic parameters, properties, storage conditions and corresponding answers.
| Q: What is the molecular formula of Halazone? |
| A: Molecular formula of Halazone is C7H5Cl2NO4S. |
| Q: What is the LogP of Halazone? |
| A: LogP of Halazone is 2.76390. |
| Q: What is the polar surface area (PSA) of Halazone? |
| A: Polar surface area (PSA) of Halazone is 83.06000. |
| Q: What is the InChIKey of Halazone? |
| A: InChIKey of Halazone is XPDVQPODLRGWPL-UHFFFAOYSA-N. |
| Q: What is the melting point of Halazone? |
| A: Melting point of Halazone is 213ºC. |
| Q: What are the uses of Halazone? |
| A: Main uses of Halazone: Halazone is an atypical antimicrobial sulfonamide derivative and a carbonic anhydrase II inhibitor with a Kd value of 1.45 µM. Halazone protects sodium channels from inactivation. Halazone is widely used for disinfection of drinking water[1][2]. |
| Q: What is the English name of Halazone? |
| A: The English name of Halazone is Halazone. |
| Q: What is the SMILES notation of Halazone? |
| A: SMILES notation of Halazone is O=C(O)c1ccc(S(=O)(=O)N(Cl)Cl)cc1. |
| Q: What English synonyms does Halazone have? |
| A: English synonyms of Halazone: Pantocide, Benzoesaeure-(sulfonsaeure-(4)-dichloramid), Gynamide, EINECS 201-253-1, Zeptabs, p-Dichlorsulfamid-benzoesaeure, Halazon, Pantosid, Pentocid, 4-dichlorosulfamoyl-benzoic acid, PANTOCID, 4-Dichlorsulfamoyl-benzoesaeure, Halozone, MFCD00045858, 4-[(dichloroamino)sulfonyl]-benzoic acid. |
| Q: What is the molecular weight of Halazone? |
| A: Molecular weight of Halazone is 270.09000. |
This table lists manufacturers and suppliers of this compound, including vendor names and product supply reference information.
| Shanghai Nianxing Industrial Co., Ltd |
| Henan Tianfu Chemical Co., Ltd. |