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Key Documents

T30007

Sigma-Aldrich

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

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>

Pictograms

Exclamation mark

Signal Word

Warning

Hazard 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

Certificates of Analysis (COA)

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Giovanni Puccio et al.
Rapid communications in mass spectrometry : RCM, 27(3), 476-480 (2013-01-03)
Thiodiglycolic acid (TDGA) is a urinary metabolite of the oxazaphosphorine class of chemotherapeutics, in particular of ifosfamide. Ifosfamide metabolism generates chloroacetaldehyde (CAA), a toxic compound associated with neurotoxicity, nephrotoxicity, urotoxicity and cardiotoxicity. CAA, in turn, interacts with cellular thiol groups
C Scheick et al.
Zeitschrift fur Naturforschung. C, Journal of biosciences, 52(1-2), 70-76 (1997-01-01)
Urine samples of premature babies contain high amounts of thiodiacetic acid (TDA). Since these pre-term infants are exposed to an increased oxygen atmosphere in the incubator, we supposed that these high levels of thiodiacetic acid might be produced from ethylene
K Norpoth et al.
Journal of cancer research and clinical oncology, 114(2), 158-162 (1988-01-01)
Two groups of male and female Sprague-Dawley rats (50 animals/group per sex) were treated with either 15.37 or 46.77 mumole of 1,1,2-TCE in DMSO/rat for 2 years. The animals were treated once a week by s.c. injection of test compound
Yu-Chen Lei et al.
Mutation research, 561(1-2), 119-126 (2004-07-09)
The association between vinyl chloride monomer (VCM) exposure and DNA damage has been established. However, the relationship between individual exposure and DNA single strand breaks was limited. Since environmental monitoring may not reflect the actual exposure, a useful marker of
June Dunnick et al.
Toxicological sciences : an official journal of the Society of Toxicology, 81(1), 243-252 (2004-06-18)
Cardiotoxicity induced by 2-, 3-, 5-, and 12-day dermal administration of 400 and 600 mg/kg/day of bis(2-chloroethoxy)methane to F344/N male and female rats was characterized. The severity and incidence of lesions were similar among males and females and in all

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