T30007
2,2′-Thiodiacetic acid
98%
Synonym(s):
2,2′-Thio-bis(acetic acid), Dicarboxydimethyl sulfide, Thiodiglycolic acid
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About This Item
Linear Formula:
S(CH2COOH)2
CAS Number:
Molecular Weight:
150.15
Beilstein:
1764392
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
Assay
98%
mp
128-131 °C (lit.)
SMILES string
OC(=O)CSCC(O)=O
InChI
1S/C4H6O4S/c5-3(6)1-9-2-4(7)8/h1-2H2,(H,5,6)(H,7,8)
InChI key
UVZICZIVKIMRNE-UHFFFAOYSA-N
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Related Categories
Application
<ul>
<li><strong>Environmentally Safe Herbicides:</strong> It is used in the synthesis of quaternary ammonium mono- and bis-salts. This compound has been formulated into ammonium 2,2-thiodiacetates, serving as selective and environmentally safe herbicides. Its application underscores its utility in sustainable agriculture and safety in environmental management (Balczewski et al., 2018).</li>
</ul>
<li><strong>Environmentally Safe Herbicides:</strong> It is used in the synthesis of quaternary ammonium mono- and bis-salts. This compound has been formulated into ammonium 2,2-thiodiacetates, serving as selective and environmentally safe herbicides. Its application underscores its utility in sustainable agriculture and safety in environmental management (Balczewski et al., 2018).</li>
</ul>
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 2
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Thiodiglycolic acid as a possible causative agent of fixed drug eruption provoked only after continuous administration of S-carboxymethyl-L-cysteine: case report and review of reported cases.
A Adachi et al.
The British journal of dermatology, 153(1), 226-228 (2005-07-21)
T Lee et al.
Biotechnology progress, 16(3), 363-367 (2000-06-03)
A Gram-negative bacterium, Alcaligenes xylosoxydans ssp. xylosoxydans (SH91), consumed thiodiglycol (TDG), the nontoxic hydrolysis product of sulfur mustard, as a primary carbon source and transformed TDG to commercially relevant chemical precursors, [(2-hydroxyethyl)thio]acetic acid (HETA) and thiodiglycolic acid (TDGA). Aerobic fed
T M Visarius et al.
Drug metabolism and disposition: the biological fate of chemicals, 26(3), 193-196 (1998-04-04)
Thiodiglycolic acid has been identified as a major metabolite of the anticancer drug ifosfamide in humans. Patients treated with 12-16 g ifosfamide/m2.day excreted thiodiglycolic acid ranging from 0.10 +/- 0.02 mmol on the first day of therapy, to a maximum
L W Wormhoudt et al.
Drug metabolism and disposition: the biological fate of chemicals, 25(4), 508-515 (1997-04-01)
1,2-Dibromoethane (1,2-DBE) is a carcinogenic compound that is metabolized both by cytochrome P450 (P450) and glutathione S-transferase (GST) enzymes, and that has been used by us as a model compound to study interindividual variability in biotransformation reactions. In this study
T Navrátil et al.
Physiological research, 59(3), 431-442 (2009-03-03)
The administration of creatine (5 g/day for one month) to 11 young active sportsmen affected their urinary excretion of creatine, creatinine, and thiodiglycolic acid (TDGA) as well as blood levels of homocysteine, vitamin B12 and folates. The probands were divided
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