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Suppliers for
2-Aminothiophenol
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Properties | CAS |
137-07-5 | Formula |
C6H7NS | EINECS |
205-277-3 |
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18 Registered suppliers
2-Aminothiophenol is an organosulfur compound with the formula C6H4(SH)(NH2). It is a colorless oily solid, although impure samples can be deeply colored. It is soluble in organic solvents and in basic water. It is a precursor to benzothiazoles, some of which are bioactive or are dyes. Isomers of aminothiophenols include 3-aminothiophenol and 4-aminothiophenol.
2-Aminothiophenol can prepared in two steps, starting with the reaction of aniline with carbon disulfide followed by hydrolysis of the resulting mercaptobenzothiazole. It can also obtained by zinc reduction of 2-nitrobenzenesulfonyl chloride.
| Appearance & Physical State | clear yellow to amber liquid
| Density | 1.16
| Melting Point | 23-26ºC
| Boiling Point | 234ºC
| Flash Point | 79ºC
| Refractive Index | 1.64-1.644
| Water Solubility | INSOLUBLE
| Stability | Stable at room temperature in closed containers under normal storage and handling conditions.
| Storage Condition | Keep away from heat, sparks, and flame. Keep away from sources of ignition. Keep container closed when not in use. Store in a cool, dry, well-ventilated area away from incompatible substances. Corrosives area. Do not expose to air. Store under an inert atm
| Vapor Pressure | 0.0517mmHg at 25°C |
2-Aminothiophenol is an organosulfur compound with the formula C6H4(SH)(NH2). It is a colorless oily solid, although impure samples can be deeply colored. It is soluble in organic solvents and in basic water. It is a precursor to benzothiazoles, some of which are bioactive or are dyes. Isomers of aminothiophenols include 3-aminothiophenol and 4-aminothiophenol.
2-Aminothiophenol can prepared in two steps, starting with the reaction of aniline with carbon disulfide followed by hydrolysis of the resulting mercaptobenzothiazole. It can also obtained by zinc reduction of 2-nitrobenzenesulfonyl chloride.
| Appearance & Physical State | clear yellow to amber liquid
| Density | 1.16
| Melting Point | 23-26ºC
| Boiling Point | 234ºC
| Flash Point | 79ºC
| Refractive Index | 1.64-1.644
| Water Solubility | INSOLUBLE
| Stability | Stable at room temperature in closed containers under normal storage and handling conditions.
| Storage Condition | Keep away from heat, sparks, and flame. Keep away from sources of ignition. Keep container closed when not in use. Store in a cool, dry, well-ventilated area away from incompatible substances. Corrosives area. Do not expose to air. Store under an inert atm
| Vapor Pressure | 0.0517mmHg at 25°C |
2-Aminothiophenol is an organosulfur compound with the formula C6H4(SH)(NH2). It is a colorless oily solid, although impure samples can be deeply colored. It is soluble in organic solvents and in basic water. It is a precursor to benzothiazoles, some of which are bioactive or are dyes. Isomers of aminothiophenols include 3-aminothiophenol and 4-aminothiophenol.
2-Aminothiophenol can prepared in two steps, starting with the reaction of aniline with carbon disulfide followed by hydrolysis of the resulting mercaptobenzothiazole. It can also obtained by zinc reduction of 2-nitrobenzenesulfonyl chloride.
| Appearance & Physical State | clear yellow to amber liquid
| Density | 1.16
| Melting Point | 23-26ºC
| Boiling Point | 234ºC
| Flash Point | 79ºC
| Refractive Index | 1.64-1.644
| Water Solubility | INSOLUBLE
| Stability | Stable at room temperature in closed containers under normal storage and handling conditions.
| Storage Condition | Keep away from heat, sparks, and flame. Keep away from sources of ignition. Keep container closed when not in use. Store in a cool, dry, well-ventilated area away from incompatible substances. Corrosives area. Do not expose to air. Store under an inert atm
| Vapor Pressure | 0.0517mmHg at 25°C |
2-Aminothiophenol is an organosulfur compound with the formula C6H4(SH)(NH2). It is a colorless oily solid, although impure samples can be deeply colored. It is soluble in organic solvents and in basic water. It is a precursor to benzothiazoles, some of which are bioactive or are dyes. Isomers of aminothiophenols include 3-aminothiophenol and 4-aminothiophenol.
2-Aminothiophenol can prepared in two steps, starting with the reaction of aniline with carbon disulfide followed by hydrolysis of the resulting mercaptobenzothiazole. It can also obtained by zinc reduction of 2-nitrobenzenesulfonyl chloride.
| Appearance & Physical State | clear yellow to amber liquid
| Density | 1.16
| Melting Point | 23-26ºC
| Boiling Point | 234ºC
| Flash Point | 79ºC
| Refractive Index | 1.64-1.644
| Water Solubility | INSOLUBLE
| Stability | Stable at room temperature in closed containers under normal storage and handling conditions.
| Storage Condition | Keep away from heat, sparks, and flame. Keep away from sources of ignition. Keep container closed when not in use. Store in a cool, dry, well-ventilated area away from incompatible substances. Corrosives area. Do not expose to air. Store under an inert atm
| Vapor Pressure | 0.0517mmHg at 25°C |
2-Aminothiophenol is an organosulfur compound with the formula C6H4(SH)(NH2). It is a colorless oily solid, although impure samples can be deeply colored. It is soluble in organic solvents and in basic water. It is a precursor to benzothiazoles, some of which are bioactive or are dyes. Isomers of aminothiophenols include 3-aminothiophenol and 4-aminothiophenol.
2-Aminothiophenol can prepared in two steps, starting with the reaction of aniline with carbon disulfide followed by hydrolysis of the resulting mercaptobenzothiazole. It can also obtained by zinc reduction of 2-nitrobenzenesulfonyl chloride.
| Appearance & Physical State | clear yellow to amber liquid
| Density | 1.16
| Melting Point | 23-26ºC
| Boiling Point | 234ºC
| Flash Point | 79ºC
| Refractive Index | 1.64-1.644
| Water Solubility | INSOLUBLE
| Stability | Stable at room temperature in closed containers under normal storage and handling conditions.
| Storage Condition | Keep away from heat, sparks, and flame. Keep away from sources of ignition. Keep container closed when not in use. Store in a cool, dry, well-ventilated area away from incompatible substances. Corrosives area. Do not expose to air. Store under an inert atm
| Vapor Pressure | 0.0517mmHg at 25°C |
2-Aminothiophenol is an organosulfur compound with the formula C6H4(SH)(NH2). It is a colorless oily solid, although impure samples can be deeply colored. It is soluble in organic solvents and in basic water. It is a precursor to benzothiazoles, some of which are bioactive or are dyes. Isomers of aminothiophenols include 3-aminothiophenol and 4-aminothiophenol.
2-Aminothiophenol can prepared in two steps, starting with the reaction of aniline with carbon disulfide followed by hydrolysis of the resulting mercaptobenzothiazole. It can also obtained by zinc reduction of 2-nitrobenzenesulfonyl chloride.
| Appearance & Physical State | clear yellow to amber liquid
| Density | 1.16
| Melting Point | 23-26ºC
| Boiling Point | 234ºC
| Flash Point | 79ºC
| Refractive Index | 1.64-1.644
| Water Solubility | INSOLUBLE
| Stability | Stable at room temperature in closed containers under normal storage and handling conditions.
| Storage Condition | Keep away from heat, sparks, and flame. Keep away from sources of ignition. Keep container closed when not in use. Store in a cool, dry, well-ventilated area away from incompatible substances. Corrosives area. Do not expose to air. Store under an inert atm
| Vapor Pressure | 0.0517mmHg at 25°C |
2-Aminothiophenol is an organosulfur compound with the formula C6H4(SH)(NH2). It is a colorless oily solid, although impure samples can be deeply colored. It is soluble in organic solvents and in basic water. It is a precursor to benzothiazoles, some of which are bioactive or are dyes. Isomers of aminothiophenols include 3-aminothiophenol and 4-aminothiophenol.
2-Aminothiophenol can prepared in two steps, starting with the reaction of aniline with carbon disulfide followed by hydrolysis of the resulting mercaptobenzothiazole. It can also obtained by zinc reduction of 2-nitrobenzenesulfonyl chloride.
| Appearance & Physical State | clear yellow to amber liquid
| Density | 1.16
| Melting Point | 23-26ºC
| Boiling Point | 234ºC
| Flash Point | 79ºC
| Refractive Index | 1.64-1.644
| Water Solubility | INSOLUBLE
| Stability | Stable at room temperature in closed containers under normal storage and handling conditions.
| Storage Condition | Keep away from heat, sparks, and flame. Keep away from sources of ignition. Keep container closed when not in use. Store in a cool, dry, well-ventilated area away from incompatible substances. Corrosives area. Do not expose to air. Store under an inert atm
| Vapor Pressure | 0.0517mmHg at 25°C |
2-Aminothiophenol is an organosulfur compound with the formula C6H4(SH)(NH2). It is a colorless oily solid, although impure samples can be deeply colored. It is soluble in organic solvents and in basic water. It is a precursor to benzothiazoles, some of which are bioactive or are dyes. Isomers of aminothiophenols include 3-aminothiophenol and 4-aminothiophenol.
2-Aminothiophenol can prepared in two steps, starting with the reaction of aniline with carbon disulfide followed by hydrolysis of the resulting mercaptobenzothiazole. It can also obtained by zinc reduction of 2-nitrobenzenesulfonyl chloride.
| Appearance & Physical State | clear yellow to amber liquid
| Density | 1.16
| Melting Point | 23-26ºC
| Boiling Point | 234ºC
| Flash Point | 79ºC
| Refractive Index | 1.64-1.644
| Water Solubility | INSOLUBLE
| Stability | Stable at room temperature in closed containers under normal storage and handling conditions.
| Storage Condition | Keep away from heat, sparks, and flame. Keep away from sources of ignition. Keep container closed when not in use. Store in a cool, dry, well-ventilated area away from incompatible substances. Corrosives area. Do not expose to air. Store under an inert atm
| Vapor Pressure | 0.0517mmHg at 25°C |
2-Aminothiophenol is an organosulfur compound with the formula C6H4(SH)(NH2). It is a colorless oily solid, although impure samples can be deeply colored. It is soluble in organic solvents and in basic water. It is a precursor to benzothiazoles, some of which are bioactive or are dyes. Isomers of aminothiophenols include 3-aminothiophenol and 4-aminothiophenol.
2-Aminothiophenol can prepared in two steps, starting with the reaction of aniline with carbon disulfide followed by hydrolysis of the resulting mercaptobenzothiazole. It can also obtained by zinc reduction of 2-nitrobenzenesulfonyl chloride.
| Appearance & Physical State | clear yellow to amber liquid
| Density | 1.16
| Melting Point | 23-26ºC
| Boiling Point | 234ºC
| Flash Point | 79ºC
| Refractive Index | 1.64-1.644
| Water Solubility | INSOLUBLE
| Stability | Stable at room temperature in closed containers under normal storage and handling conditions.
| Storage Condition | Keep away from heat, sparks, and flame. Keep away from sources of ignition. Keep container closed when not in use. Store in a cool, dry, well-ventilated area away from incompatible substances. Corrosives area. Do not expose to air. Store under an inert atm
| Vapor Pressure | 0.0517mmHg at 25°C |
2-Aminothiophenol is an organosulfur compound with the formula C6H4(SH)(NH2). It is a colorless oily solid, although impure samples can be deeply colored. It is soluble in organic solvents and in basic water. It is a precursor to benzothiazoles, some of which are bioactive or are dyes. Isomers of aminothiophenols include 3-aminothiophenol and 4-aminothiophenol.
2-Aminothiophenol can prepared in two steps, starting with the reaction of aniline with carbon disulfide followed by hydrolysis of the resulting mercaptobenzothiazole. It can also obtained by zinc reduction of 2-nitrobenzenesulfonyl chloride.
| Appearance & Physical State | clear yellow to amber liquid
| Density | 1.16
| Melting Point | 23-26ºC
| Boiling Point | 234ºC
| Flash Point | 79ºC
| Refractive Index | 1.64-1.644
| Water Solubility | INSOLUBLE
| Stability | Stable at room temperature in closed containers under normal storage and handling conditions.
| Storage Condition | Keep away from heat, sparks, and flame. Keep away from sources of ignition. Keep container closed when not in use. Store in a cool, dry, well-ventilated area away from incompatible substances. Corrosives area. Do not expose to air. Store under an inert atm
| Vapor Pressure | 0.0517mmHg at 25°C |
2-Aminothiophenol is an organosulfur compound with the formula C6H4(SH)(NH2). It is a colorless oily solid, although impure samples can be deeply colored. It is soluble in organic solvents and in basic water. It is a precursor to benzothiazoles, some of which are bioactive or are dyes. Isomers of aminothiophenols include 3-aminothiophenol and 4-aminothiophenol.
2-Aminothiophenol can prepared in two steps, starting with the reaction of aniline with carbon disulfide followed by hydrolysis of the resulting mercaptobenzothiazole. It can also obtained by zinc reduction of 2-nitrobenzenesulfonyl chloride.
| Appearance & Physical State | clear yellow to amber liquid
| Density | 1.16
| Melting Point | 23-26ºC
| Boiling Point | 234ºC
| Flash Point | 79ºC
| Refractive Index | 1.64-1.644
| Water Solubility | INSOLUBLE
| Stability | Stable at room temperature in closed containers under normal storage and handling conditions.
| Storage Condition | Keep away from heat, sparks, and flame. Keep away from sources of ignition. Keep container closed when not in use. Store in a cool, dry, well-ventilated area away from incompatible substances. Corrosives area. Do not expose to air. Store under an inert atm
| Vapor Pressure | 0.0517mmHg at 25°C |
2-Aminothiophenol is an organosulfur compound with the formula C6H4(SH)(NH2). It is a colorless oily solid, although impure samples can be deeply colored. It is soluble in organic solvents and in basic water. It is a precursor to benzothiazoles, some of which are bioactive or are dyes. Isomers of aminothiophenols include 3-aminothiophenol and 4-aminothiophenol.
2-Aminothiophenol can prepared in two steps, starting with the reaction of aniline with carbon disulfide followed by hydrolysis of the resulting mercaptobenzothiazole. It can also obtained by zinc reduction of 2-nitrobenzenesulfonyl chloride.
| Appearance & Physical State | clear yellow to amber liquid
| Density | 1.16
| Melting Point | 23-26ºC
| Boiling Point | 234ºC
| Flash Point | 79ºC
| Refractive Index | 1.64-1.644
| Water Solubility | INSOLUBLE
| Stability | Stable at room temperature in closed containers under normal storage and handling conditions.
| Storage Condition | Keep away from heat, sparks, and flame. Keep away from sources of ignition. Keep container closed when not in use. Store in a cool, dry, well-ventilated area away from incompatible substances. Corrosives area. Do not expose to air. Store under an inert atm
| Vapor Pressure | 0.0517mmHg at 25°C |
2-Aminothiophenol is an organosulfur compound with the formula C6H4(SH)(NH2). It is a colorless oily solid, although impure samples can be deeply colored. It is soluble in organic solvents and in basic water. It is a precursor to benzothiazoles, some of which are bioactive or are dyes. Isomers of aminothiophenols include 3-aminothiophenol and 4-aminothiophenol.
2-Aminothiophenol can prepared in two steps, starting with the reaction of aniline with carbon disulfide followed by hydrolysis of the resulting mercaptobenzothiazole. It can also obtained by zinc reduction of 2-nitrobenzenesulfonyl chloride.
| Appearance & Physical State | clear yellow to amber liquid
| Density | 1.16
| Melting Point | 23-26ºC
| Boiling Point | 234ºC
| Flash Point | 79ºC
| Refractive Index | 1.64-1.644
| Water Solubility | INSOLUBLE
| Stability | Stable at room temperature in closed containers under normal storage and handling conditions.
| Storage Condition | Keep away from heat, sparks, and flame. Keep away from sources of ignition. Keep container closed when not in use. Store in a cool, dry, well-ventilated area away from incompatible substances. Corrosives area. Do not expose to air. Store under an inert atm
| Vapor Pressure | 0.0517mmHg at 25°C |
2-Aminothiophenol is an organosulfur compound with the formula C6H4(SH)(NH2). It is a colorless oily solid, although impure samples can be deeply colored. It is soluble in organic solvents and in basic water. It is a precursor to benzothiazoles, some of which are bioactive or are dyes. Isomers of aminothiophenols include 3-aminothiophenol and 4-aminothiophenol.
2-Aminothiophenol can prepared in two steps, starting with the reaction of aniline with carbon disulfide followed by hydrolysis of the resulting mercaptobenzothiazole. It can also obtained by zinc reduction of 2-nitrobenzenesulfonyl chloride.
| Appearance & Physical State | clear yellow to amber liquid
| Density | 1.16
| Melting Point | 23-26ºC
| Boiling Point | 234ºC
| Flash Point | 79ºC
| Refractive Index | 1.64-1.644
| Water Solubility | INSOLUBLE
| Stability | Stable at room temperature in closed containers under normal storage and handling conditions.
| Storage Condition | Keep away from heat, sparks, and flame. Keep away from sources of ignition. Keep container closed when not in use. Store in a cool, dry, well-ventilated area away from incompatible substances. Corrosives area. Do not expose to air. Store under an inert atm
| Vapor Pressure | 0.0517mmHg at 25°C |
2-Aminothiophenol is an organosulfur compound with the formula C6H4(SH)(NH2). It is a colorless oily solid, although impure samples can be deeply colored. It is soluble in organic solvents and in basic water. It is a precursor to benzothiazoles, some of which are bioactive or are dyes. Isomers of aminothiophenols include 3-aminothiophenol and 4-aminothiophenol.
2-Aminothiophenol can prepared in two steps, starting with the reaction of aniline with carbon disulfide followed by hydrolysis of the resulting mercaptobenzothiazole. It can also obtained by zinc reduction of 2-nitrobenzenesulfonyl chloride.
| Appearance & Physical State | clear yellow to amber liquid
| Density | 1.16
| Melting Point | 23-26ºC
| Boiling Point | 234ºC
| Flash Point | 79ºC
| Refractive Index | 1.64-1.644
| Water Solubility | INSOLUBLE
| Stability | Stable at room temperature in closed containers under normal storage and handling conditions.
| Storage Condition | Keep away from heat, sparks, and flame. Keep away from sources of ignition. Keep container closed when not in use. Store in a cool, dry, well-ventilated area away from incompatible substances. Corrosives area. Do not expose to air. Store under an inert atm
| Vapor Pressure | 0.0517mmHg at 25°C |
2-Aminothiophenol is an organosulfur compound with the formula C6H4(SH)(NH2). It is a colorless oily solid, although impure samples can be deeply colored. It is soluble in organic solvents and in basic water. It is a precursor to benzothiazoles, some of which are bioactive or are dyes. Isomers of aminothiophenols include 3-aminothiophenol and 4-aminothiophenol.
2-Aminothiophenol can prepared in two steps, starting with the reaction of aniline with carbon disulfide followed by hydrolysis of the resulting mercaptobenzothiazole. It can also obtained by zinc reduction of 2-nitrobenzenesulfonyl chloride.
| Appearance & Physical State | clear yellow to amber liquid
| Density | 1.16
| Melting Point | 23-26ºC
| Boiling Point | 234ºC
| Flash Point | 79ºC
| Refractive Index | 1.64-1.644
| Water Solubility | INSOLUBLE
| Stability | Stable at room temperature in closed containers under normal storage and handling conditions.
| Storage Condition | Keep away from heat, sparks, and flame. Keep away from sources of ignition. Keep container closed when not in use. Store in a cool, dry, well-ventilated area away from incompatible substances. Corrosives area. Do not expose to air. Store under an inert atm
| Vapor Pressure | 0.0517mmHg at 25°C |
2-Aminothiophenol is an organosulfur compound with the formula C6H4(SH)(NH2). It is a colorless oily solid, although impure samples can be deeply colored. It is soluble in organic solvents and in basic water. It is a precursor to benzothiazoles, some of which are bioactive or are dyes. Isomers of aminothiophenols include 3-aminothiophenol and 4-aminothiophenol.
2-Aminothiophenol can prepared in two steps, starting with the reaction of aniline with carbon disulfide followed by hydrolysis of the resulting mercaptobenzothiazole. It can also obtained by zinc reduction of 2-nitrobenzenesulfonyl chloride.
| Appearance & Physical State | clear yellow to amber liquid
| Density | 1.16
| Melting Point | 23-26ºC
| Boiling Point | 234ºC
| Flash Point | 79ºC
| Refractive Index | 1.64-1.644
| Water Solubility | INSOLUBLE
| Stability | Stable at room temperature in closed containers under normal storage and handling conditions.
| Storage Condition | Keep away from heat, sparks, and flame. Keep away from sources of ignition. Keep container closed when not in use. Store in a cool, dry, well-ventilated area away from incompatible substances. Corrosives area. Do not expose to air. Store under an inert atm
| Vapor Pressure | 0.0517mmHg at 25°C |
2-Aminothiophenol is an organosulfur compound with the formula C6H4(SH)(NH2). It is a colorless oily solid, although impure samples can be deeply colored. It is soluble in organic solvents and in basic water. It is a precursor to benzothiazoles, some of which are bioactive or are dyes. Isomers of aminothiophenols include 3-aminothiophenol and 4-aminothiophenol.
2-Aminothiophenol can prepared in two steps, starting with the reaction of aniline with carbon disulfide followed by hydrolysis of the resulting mercaptobenzothiazole. It can also obtained by zinc reduction of 2-nitrobenzenesulfonyl chloride.
| Appearance & Physical State | clear yellow to amber liquid
| Density | 1.16
| Melting Point | 23-26ºC
| Boiling Point | 234ºC
| Flash Point | 79ºC
| Refractive Index | 1.64-1.644
| Water Solubility | INSOLUBLE
| Stability | Stable at room temperature in closed containers under normal storage and handling conditions.
| Storage Condition | Keep away from heat, sparks, and flame. Keep away from sources of ignition. Keep container closed when not in use. Store in a cool, dry, well-ventilated area away from incompatible substances. Corrosives area. Do not expose to air. Store under an inert atm
| Vapor Pressure | 0.0517mmHg at 25°C |
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Last update 2024-04-26
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