64306
甲基硫代磺酸甲酯
purum, ≥98.0% (GC)
别名:
S-甲基硫代甲基砜, MMTS
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关于此项目
线性分子式:
CH3SO2SCH3
化学文摘社编号:
分子量:
126.20
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
220-970-0
Beilstein/REAXYS Number:
1446059
MDL number:
Assay:
≥98.0% (GC)
grade
purum
Quality Level
assay
≥98.0% (GC)
refractive index
n20/D 1.513
bp
69-71 °C/0.4 mmHg (lit.)
solubility
chloroform: 750mg + 5 ml Chloroform mg/mL, colorless to light greenish-yellow
density
1.337 g/mL at 20 °C, 1.337 g/mL at 25 °C (lit.)
functional group
disulfide
storage temp.
2-8°C
SMILES string
CSS(C)(=O)=O
InChI
1S/C2H6O2S2/c1-5-6(2,3)4/h1-2H3
InChI key
XYONNSVDNIRXKZ-UHFFFAOYSA-N
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Application
- 硫氢基酶的修饰：甲基硫代磺酸甲酯（MMTS）提供了一种修饰硫氢基酶和氧化还原调节蛋白的独特方法 ，提供了有关于酶调节和氧化还原生物学的生化研究中的潜在应用（Makarov et al., 2019）。
- 用于蛋白酶活性的传感器开发： 甲基硫代磺酸甲酯被用作木瓜蛋白酶样半胱氨酸蛋白酶结构转化的阻滞剂，这有助于其在传感器开发中的用途，使我们可以检测和分析各种生物过程中的蛋白酶的活性（Markovic et al., 2023）。
- 农业病原体控制：研究评估了作为晚期枯萎病抑制剂的甲基硫代磺酸甲酯，重点介绍了其作为植物病原体广泛毒素的潜力，暗示了其在农业农作物疾病管理中的应用（Joller et al., 2020）。
Other Notes
亚甲基亚磺酰化剂有多种用途 ；对于 α-环酮的甲磺酰化 ；硫醇中的甲基二硫化物；酶的选择性、可逆性失活
Disclaimer
储存时可能变为黄色
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 3 Oral - Skin Sens. 1
存储类别
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
wgk
WGK 3
P. Laszlo et al.
The Journal of Organic Chemistry, 49, 2281-2281 (1984)
D. Scholz
Synthesis, 944-944 (1983)
Anna-Riikka Karala et al.
Antioxidants & redox signaling, 9(4), 527-531 (2007-02-07)
S-Methyl methanethiosulfonate (MMTS) is a reagent used to trap the natural thiol-disulfide state of the proteins. The efficiency of trapping mixed disulfides in vivo has been found to be higher for MMTS than for the more commonly used N-ethylmaleimide. MMTS
W H Briggs et al.
Journal of agricultural and food chemistry, 48(11), 5731-5735 (2000-11-23)
Thiosulfinates (TSs) have been implicated as a principle source of the antiplatelet property of raw onion and garlic juice. The in vitro responses of human platelets to dosages of four TSs were measured using whole blood aggregometry and compared by
D J Smith et al.
Biochemistry, 14(4), 766-771 (1975-02-25)
New reagents for the temporary blocking of active or accessible sulfhydryl groups of enzymes have been developed. These reagents, which are either alkyl alkanethiolsulfonates or alkoxycarbonylalkyl disulfides, rapidly and quantitatively place various RS- groups on the sulfhydryls to generate mixed
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| 778672-25KG | 04061833367568 |
| W326305-1KG | 04061835566839 |
| W326305-100G | 04061837528651 |
| V900400-500G | 04061832649580 |
| 30089-25G | 04061826660591 |
| 168149-500G | 04061835554416 |
| 168149-100G | 04061835521173 |
| 243005-1KG | 04055977199079 |
| 243005-100GM | 04055977199086 |
| 243005-25GM | 07790788054939 |
| 30089-1G-KC | 04061826680261 |
| 30089-500G | 04061833440315 |
| 30089-100G | 04061826660096 |
| 1028381000 | 04022536037387 |
| 1028380100 | 04022536037370 |
| 1028389010 | 04022536692678 |
| 778672-100G | 04061833315064 |
| C7352-100G | 04061835568321 |
| C7352-25G | 04061835568338 |
| 1024520025 | 04027269669775 |
| 1024520250 | 04027269965280 |
| 1028380025 | 04022536037363 |
| C5360-100G | 04061833502013 |
| C7352-1G | 04061822459366 |
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