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Name | Methyl thioglycolate |
Basic Information | |
Synonyms | MERCAPTOACETIC ACID METHYL ESTER; METG; METHYL THIOGLYCOLATE; |
CAS number | 2365-48-2 |
EINECS | 219-121-7 |
Formula | C3H6O2S |
Molecular Weight | 106.14 |
Melting Point | -24 °C |
Flashing Point | 86 °F |
Water Solubility | 40 g/L (20 ºC) |
Boiling Point | 42-43 °C10 mm Hg(lit.) |
Density | 1.187 g/mL at 25 °C(lit.) |
Storage temp | Store below +30°C. |
Refractive index | n20/D 1.466(lit.) |
Safety Information | |
Hazard Codes | Xn,T |
Risk Statements | 10-20/22-36/37/38-25 |
Safety Statements | 26-36/37-45-36/37/39-28A |
RIDADR | UN 1992 3/PG 3 |
RTECS | AI7350000 |
HazardClass | 3 |
PackingGroup | III |
HS Code | 29309070 |
Description | |
Methyl Thioglycolate is an derivative of Thioglycolic Acid (T350760), an organic compound containing both a thiol and a carboxylic acid functional groups. Thioglycolic Acid and its derivatives are oft en used in organic synthesis as a nucleophile in thioglycolysis reactions and is also used as a S transfer agent for sulfonyl chloride synthesis. Methyl Thioglycolate have been studied for the its inf luence on neocarzinostatin activation and expression of DNA damage. |
Name | Methyl thioglycolate |
Basic Information | |
Synonyms | MERCAPTOACETIC ACID METHYL ESTER; METG; METHYL THIOGLYCOLATE; |
CAS number | 2365-48-2 |
EINECS | 219-121-7 |
Formula | C3H6O2S |
Molecular Weight | 106.14 |
Melting Point | -24 °C |
Flashing Point | 86 °F |
Water Solubility | 40 g/L (20 ºC) |
Boiling Point | 42-43 °C10 mm Hg(lit.) |
Density | 1.187 g/mL at 25 °C(lit.) |
Storage temp | Store below +30°C. |
Refractive index | n20/D 1.466(lit.) |
Safety Information | |
Hazard Codes | Xn,T |
Risk Statements | 10-20/22-36/37/38-25 |
Safety Statements | 26-36/37-45-36/37/39-28A |
RIDADR | UN 1992 3/PG 3 |
RTECS | AI7350000 |
HazardClass | 3 |
PackingGroup | III |
HS Code | 29309070 |
Description | |
Methyl Thioglycolate is an derivative of Thioglycolic Acid (T350760), an organic compound containing both a thiol and a carboxylic acid functional groups. Thioglycolic Acid and its derivatives are oft en used in organic synthesis as a nucleophile in thioglycolysis reactions and is also used as a S transfer agent for sulfonyl chloride synthesis. Methyl Thioglycolate have been studied for the its inf luence on neocarzinostatin activation and expression of DNA damage. |
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