3-hydroxythiophenol

phenol, 3-mercapto-

CAS: 40248-84-8 C6 H6 O S MW: 126.17802000

Identification

Name3-hydroxythiophenol
IUPAC3-sulfanylphenol
CAS Number40248-84-8
FDA UNIISearch
Molecular FormulaC6 H6 O S
Molecular Weight126.17802000
MDL NumberMFCD01317829
Nikkaji NumberJ801.846D
XlogP31.30 (est)

Regulatory

Physical Properties

Assay 95.00 to 100.00
Food Chemicals Codex Listed No
Melting Point 17.00 °C. @ 760.00 mm Hg
Boiling Point 256.00 to 257.00 °C. @ 760.00 mm Hg (est), 135.00 °C. @ 35.00 mm Hg
Vapor Pressure 0.010000 mmHg @ 25.00 °C. (est)
Flash Point 228.00 °F. TCC ( 108.80 °C. ) (est)
logP (o/w) 1.814 (est)
Soluble in water, 4733 mg/L @ 25 °C (est)

No sensory data available

Safety Information

Preferred SDSView
Oral/Parenteral ToxicityNot determined
Dermal ToxicityNot determined
Inhalation ToxicityNot determined

GHS Classification

['GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)', 'GHS Label elements, including precautionary statements']

Safety in Use

Categoryinformation only not used for fragrances or flavors
Recommendation for 3-hydroxythiophenol usage levels up tonot for fragrance use.
Recommendation for 3-hydroxythiophenol flavor usage levels up tonot for flavor use.

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Potential Uses

None Found

Natural Occurrence

not found in nature

Synonyms

3- hydroxybenzene thiol 3- hydroxybenzenethiol meta- hydroxythiophenol 3- mercaptophenol meta- mercaptophenol phenol, 3-mercapto- 3- sulfanylphenol PubMed: Detecting trace melamine in solution by SERS using Ag nanoparticle coated poly(styrene-co-acrylic acid) nanospheres as novel active substrates. PubMed: Charge-transfer interaction of aromatic thiols with 2,3-dichloro-5,6-dicyano-p-benzoquinone: spectral and quantum mechanical studies. PubMed: An efficient synthesis of a potent PPARpan agonist. PubMed: Solid-phase library synthesis of alkoxyprolines. PubMed: Syntheses, reactivity, and pi-donating ligand metathesis reaction of five-coordinate sixteen-electron manganese(I) complexes: crystal structures of [Mn(CO(3)(-TeC(6)H(4)-o-NH-)](-), [(Mn(CO)(3))2(mu-SC(6)H(4)-o-S--S--C(6)H(4)-o-mu-S--)], [(CO)(3)Mn(mu-SC(6)H(4)-o-NH(2)-)]2, and [(CO)(3)Mn(mu-SC(8)N(2)H(4)-o-S-)](2)(2-). PubMed: O- and S-methylated bromothiocatechols. PubMed: Exclusive production of bistranded DNA damage by calicheamicin. PubMed: Poly(amidoamine)s with potential as drug carriers: degradation and cellular toxicity.