T31003
Thiolactic acid
95%
Synonym(s):
2-Mercaptopropionic acid
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About This Item
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Quality Level
Assay
95%
refractive index
n20/D 1.481 (lit.)
bp
102 °C/16 mmHg (lit.)
203-208 °C (lit.)
mp
10-14 °C (lit.)
density
1.196 g/mL at 25 °C (lit.)
SMILES string
CC(S)C(O)=O
InChI
1S/C3H6O2S/c1-2(6)3(4)5/h2,6H,1H3,(H,4,5)
InChI key
PMNLUUOXGOOLSP-UHFFFAOYSA-N
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Application
Thiolactic acid (TLA) can be used as a building block in the synthesis of:
It can also be used as a bidental chelating agent for the surface modification of titanium dioxide (TiO2) nanoparticles for the removal of cadmium from waste water.
- Thiolactomycin via oxathiolanone intermediate.
- 4-Thiazolidinones by reacting various Schiff bases with thioglycolic acid.
- 1,4-Naphthoquinone derivatives containing sulfur atom for antibacterial and antiviral activity studies.
It can also be used as a bidental chelating agent for the surface modification of titanium dioxide (TiO2) nanoparticles for the removal of cadmium from waste water.
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Skin Corr. 1B
Storage Class Code
6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
WGK
WGK 1
Flash Point(F)
190.4 °F - closed cup
Flash Point(C)
88 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Synthesis and biological evaluation of novel 1, 4-naphthoquinone derivatives as antibacterial and antiviral agents
Bioorganic & Medicinal Chemistry Letters, 15(14), 3463-3466 (2005)
Synthesis of novel heterocyclic 4-thiazolidinone derivatives and their antibacterial activity
Journal of Chemistry, 1(4), 189-193 (2004)
A Flexible Route to (5 R)-Thiolactomycin, a Naturally Occurring Inhibitor of Fatty Acid Synthesis
Organic Letters, 4(22), 3859-3862 (2002)
Cadmium removal from water using thiolactic acid-modified titanium dioxide nanoparticles
Journal of Photochemistry and Photobiology A: Chemistry, 148(1-3), 393-397 (2002)
Chemical communications (Cambridge, England), (44)(44), 6828-6830 (2009-11-04)
Addition of O(2)(g) at low-temperature to a mononuclear, nonheme iron(ii) complex comprising a tetraazamacrocyclic N(4) donor and an arylthiolate S donor leads to the generation of a deep red complex assigned as a low-spin Fe(III)?OOH complex, formed via metal- and
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