T31003
Thiolactic acid
95%
Synonym(s):
2-Mercaptopropionic acid
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About This Item
Linear Formula:
CH3CH(SH)COOH
CAS Number:
Molecular Weight:
106.14
Beilstein:
506218
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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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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Related Categories
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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A Flexible Route to (5 R)-Thiolactomycin, a Naturally Occurring Inhibitor of Fatty Acid Synthesis
McFadden JM, et al.
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Cadmium removal from water using thiolactic acid-modified titanium dioxide nanoparticles
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Journal of Photochemistry and Photobiology A: Chemistry, 148(1-3), 393-397 (2002)
T Teerlink et al.
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A high-performance liquid chromatographic method for the determination of glutamine in biological samples is presented. Glutamine was derivatized with ortho-phthalaldehyde reagent containing 3-mercaptopropionic acid and separated by reversed phase chromatography on a C18 column containing 3-microns particles. No interference from
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