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3-Methoxythiophenol - 98%, high purity , CAS No.15570-12-4

    Grade & Purity:
  • ≥98%
In stock
Item Number
M101779
Grouped product items
SKU Size
Availability
Price Qty
M101779-1g
1g
3
$9.90
M101779-5g
5g
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$22.90
M101779-25g
25g
2
$57.90
M101779-100g
100g
1
$208.90

Basic Description

Synonyms BP-10733 | m-Methoxy phenyl mercaptan | 3-methyloxy-benzenethiol | PS-3033 | AKOS005257798 | m-Methoxythiophenol | (M-METHOXYPHENYL)THIOL | NSC-518339 | 3-Methoxy thiophenol | 3-methoxy -thiophenol | AMY21950 | 3-Mercaptoanisole | 3-METHOXYBENZENE-1-THIOL
Specifications & Purity ≥98%
Storage Temp Store at 2-8°C,Argon charged
Shipped In
Wet ice
This product requires cold chain shipping. Ground and other economy services are not available.
Product Description

3-Methoxythiophenol was used in the preparation of allenes。

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Benzenoids
Class Thiophenols
Subclass Not available
Intermediate Tree Nodes Not available
Direct Parent Thiophenols
Alternative Parents Phenoxy compounds  Methoxybenzenes  Anisoles  Alkyl aryl ethers  Thiols  Hydrocarbon derivatives  
Molecular Framework Aromatic homomonocyclic compounds
Substituents Phenoxy compound - Methoxybenzene - Thiophenol - Phenol ether - Anisole - Alkyl aryl ether - Monocyclic benzene moiety - Arylthiol - Ether - Organic oxygen compound - Hydrocarbon derivative - Organosulfur compound - Organooxygen compound - Aromatic homomonocyclic compound
Description This compound belongs to the class of organic compounds known as thiophenols. These are compounds containing a thiophenol ring, which a phenol derivative obtained by replacing the oxygen atom from the hydroxyl group (attached to the benzene) by a sulfur atom.
External Descriptors Not available

Mechanisms of Action

Mechanism of Action Action Type target ID Target Name Target Type Target Organism Binding Site Name References

Names and Identifiers

IUPAC Name 3-methoxybenzenethiol
INCHI InChI=1S/C7H8OS/c1-8-6-3-2-4-7(9)5-6/h2-5,9H,1H3
InChIKey QMVAZEHZOPDGHA-UHFFFAOYSA-N
Smiles COC1=CC(=CC=C1)S
Isomeric SMILES COC1=CC(=CC=C1)S
WGK Germany 3
UN Number 2810
Molecular Weight 140.2
Beilstein 2041496
Reaxy-Rn 2041496
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2041496&ln=

Certificates(CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

12 results found

Lot Number Certificate Type Date Item
J2312515 Certificate of Analysis Jul 09, 2025 M101779
J2312516 Certificate of Analysis Jul 09, 2025 M101779
J2312517 Certificate of Analysis Jul 09, 2025 M101779
J2312518 Certificate of Analysis Jul 09, 2025 M101779
D2301519 Certificate of Analysis Jan 07, 2025 M101779
D2301532 Certificate of Analysis Jan 07, 2025 M101779
D2301516 Certificate of Analysis Jan 07, 2025 M101779
D2301523 Certificate of Analysis Jan 07, 2025 M101779
G2417456 Certificate of Analysis Jun 13, 2024 M101779
K2104263 Certificate of Analysis Aug 04, 2023 M101779
K2104267 Certificate of Analysis Aug 04, 2023 M101779
A2104300 Certificate of Analysis Oct 19, 2022 M101779

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Chemical and Physical Properties

Solubility Not miscible or difficult to mix in water. Soluble in methanol, benzene, hexane, toluene and dichloromethane.
Sensitivity Air sensitive.
Refractive Index 1.587
Flash Point(°F) 204.8 °F
Flash Point(°C) 96 °C
Boil Point(°C) 223-226°C
Molecular Weight 140.200 g/mol
XLogP3 2.500
Hydrogen Bond Donor Count 1
Hydrogen Bond Acceptor Count 2
Rotatable Bond Count 1
Exact Mass 140.03 Da
Monoisotopic Mass 140.03 Da
Topological Polar Surface Area 10.200 Ų
Heavy Atom Count 9
Formal Charge 0
Complexity 85.000
Isotope Atom Count 0
Defined Atom Stereocenter Count 0
Undefined Atom Stereocenter Count 0
Defined Bond Stereocenter Count 0
Undefined Bond Stereocenter Count 0
The total count of all stereochemical bonds 0
Covalently-Bonded Unit Count 1

Alternative Products

Citations of This Product

1. Jun Zha, Xiangfu Meng, Wentao Fan, Qing You, Nan Xia, Wanmiao Gu, Yan Zhao, Lin Hu, Jin Li, Haiteng Deng, Hui Wang, Nan Yan, Zhikun Wu.  (2023)  Surface Site-Specific Replacement for Catalysis Selectivity Switching.  ACS Applied Materials & Interfaces,  15  (3): (3985–3992). 
2. H. Nabipour, X. Wang, L. Song, Y. Hu.  (2023)  Synthesis of a bio-based and intrinsically anti-flammable epoxy thermoset and the application of its carbonized foam as an efficient CO2 capture adsorbent.  Materials Today Sustainability,  21  (100265). 
3. Chen Xuejing, Zhou Xuesi, He Qinghua, He Yonghong, Guan Tian, Feng Guangxia, Wang Bei, Xie Luyuan, Ji Yanhong.  (2020)  Hydrogel-based microbeads for Raman-encoded suspension array using the reversed-phase suspension polymerization method and ultraviolet light curing.  ANALYTICAL AND BIOANALYTICAL CHEMISTRY,  412  (12): (2731-2741). 

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