| Identification | More | [Name]
Methyl thioglycolate | [CAS]
2365-48-2 | [Synonyms]
MERCAPTOACETIC ACID METHYL ESTER
METG
METHYL MERCAPTOACETATE
METHYL THIOGLYCOLATE
METHYL THIOGLYCOLLATE
THIOGLYCOLIC ACID METHYL ESTER
mercapto-aceticacimethylester
Methanethiol, methoxy-
methoxy-methanethio
Methyl 2-mercaptoacetate
Methyl alpha-mercaptoacetate
Methyl ester of thioglycolic acid
Methyl sulfanylacetate
methyl2-mercaptoacetate
Thioglykolsaeure-methylester
USAF ek-7119
usafek-7119
Sulfhydryl methyl acetate
Methylthioglycolate,98%
Acetic acid, mercapto-, methyl ester | [EINECS(EC#)]
219-121-7 | [Molecular Formula]
C3H6O2S | [MDL Number]
MFCD00004873 | [Molecular Weight]
106.14 | [MOL File]
2365-48-2.mol |
| Chemical Properties | Back Directory | [Appearance]
CLEAR COLOURLESS LIQUID | [Melting point ]
-24 °C
| [Boiling point ]
42-43 °C/10 mmHg (lit.) | [density ]
1.187 g/mL at 25 °C(lit.)
| [refractive index ]
n20/D 1.466(lit.)
| [Fp ]
86 °F
| [storage temp. ]
Store below +30°C. | [solubility ]
40g/l | [form ]
Liquid | [pka]
8.04±0.10(Predicted) | [color ]
Clear colorless | [Odor]
Strong, unpleasant, garlic-like | [Water Solubility ]
40 g/L (20 ºC) | [Sensitive ]
Air Sensitive | [BRN ]
506259 | [Henry's Law Constant]
1.6×100 mol/(m3Pa) at 25℃, HSDB (2015) | [Cosmetics Ingredients Functions]
HAIR WAVING OR STRAIGHTENING | [Cosmetic Ingredient Review (CIR)]
Methyl thioglycolate (2365-48-2) | [InChI]
1S/C3H6O2S/c1-5-3(4)2-6/h6H,2H2,1H3 | [InChIKey]
MKIJJIMOAABWGF-UHFFFAOYSA-N | [SMILES]
COC(=O)CS | [CAS DataBase Reference]
2365-48-2(CAS DataBase Reference) | [NIST Chemistry Reference]
Acetic acid, mercapto-, methyl ester(2365-48-2) | [EPA Substance Registry System]
2365-48-2(EPA Substance) |
| Safety Data | Back Directory | [Symbol(GHS) ]
 
GHS02,GHS06 | [Signal word ]
Danger | [Hazard statements ]
H226-H301-H315-H319-H332-H335 | [Precautionary statements ]
P210-P233-P301+P310-P303+P361+P353-P304+P340+P312-P305+P351+P338 | [Hazard Codes ]
Xn,T | [Risk Statements ]
R10:Flammable.
R20/22:Harmful by inhalation and if swallowed .
R36/37/38:Irritating to eyes, respiratory system and skin .
R25:Toxic if swallowed. | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36/37:Wear suitable protective clothing and gloves .
S45:In case of accident or if you feel unwell, seek medical advice immediately (show label where possible) .
S36/37/39:Wear suitable protective clothing, gloves and eye/face protection . | [RIDADR ]
UN 1992 3/PG 3
| [WGK Germany ]
1
| [RTECS ]
AI7350000
| [TSCA ]
Yes | [REACH Registrations]
Active | [HazardClass ]
3 | [PackingGroup ]
III | [HS Code ]
29309070 | [Storage Class]
3 - Flammable liquids | [Hazard Classifications]
Acute Tox. 3 Oral
Acute Tox. 4 Inhalation
Eye Irrit. 2
Flam. Liq. 3
Skin Irrit. 2
STOT SE 3 | [Hazardous Substances Data]
2365-48-2(Hazardous Substances Data) | [Toxicity]
mouse,LD50,intraperitoneal,100mg/kg (100mg/kg),National Technical Information Service. Vol. AD277-689, |
| Hazard Information | Back Directory | [Chemical Properties]
CLEAR COLOURLESS LIQUID | [Uses]
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. | [Application]
Methyl thioglycolate is a chemical compound that is used in the pharmaceutical industry as an intermediate. It has been used to synthesize anti-inflammatory drugs, such as aspirin and ibuprofen, and also for the treatment of autoimmune diseases. Methyl thioglycolate binds to amino acids on the surface of bacteria, which prevents them from functioning properly. This binding causes the cells to stop growing and die.
| [Definition]
Methyl thioglycolate are widely used in free-radical photoinitiated polymerization reactions. In particular, the use of methyl thioglycolate (MTG), CH3OC(O)CH2SH, results in greater photopolymerization reaction rates, attributed to a weakening of the sulfur–hydrogen bond by hydrogen bonding of the thiol group. MTG constitutes the smaller exponent of the series of CH3OC(O)(CH2)nSH compounds, reported as intermediated in the organic sulfur cycle in marine environments, produced by marine phytoplankton.
| [Production Methods]
Adding thioglycollic acid with purity of between 70.0 and 96.0 percent and methanol with purity of between 95.0 and 99.9 percent into a reaction device according to the molar ratio of 1:1.3-4.0; subsequently, adding an activating agent into the reaction device, stirring and heating for reaction; and after the reaction is finished, carrying out separatory distillation on reaction products to obtain the methyl thioglycolate. The activating agent is a p-toluenesulfonic acid methanol solution with a mass concentration of between 20 and 30 percent, and the use amount is 0.5 to 1.0 percent of the total mass of relative input materials.
| [General Description]
Methyl thioglycolate reacts with nonprotein component of the antitumor antibiotic neocarzinostatin to form 1:1 adduct. It reacts with isothiocyanate to form Rhodanine. | [reaction suitability]
reagent type: ligand
reaction type: [1,2]-Wittig Rearrangement |
|
| Company Name: |
J & K SCIENTIFIC LTD.
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| Telephone: |
18210857532 18210857532 |
| Website: |
https://www.jkchemical.com |
| Company Name: |
Alfa Aesar
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400-6106006 |
| Website: |
http://chemicals.thermofisher.cn |
| Company Name: |
Energy Chemical
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400-0056266 |
| Website: |
www.energy-chemical.com |
| Company Name: |
Jia Xing Isenchem Co.,Ltd
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| Telephone: |
0573-85285100 18627885956 |
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https://www.chemicalbook.com/ShowSupplierProductsList14265/0_EN.htm |
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