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Trimethylsulfonium hydroxide solution - 0.2mol/L in methanol, high purity , CAS No.17287-03-5

COA

Grade & Purity:

0.2mol/L in methanol

Cas Number: 17287-03-5
Molecular Weight: 94.18
Beilstein Registry Number: 3910286
MDL number: MFCD00216756
PubChem CID: 11105313
PubChem SID: 504766009

In stock

Item Number

T113600

Grouped product items
SKU	Size	Availability	Price
T113600-1ml	1ml	3	$18.90
T113600-5ml	5ml	3	$71.90
T113600-10×1ml	10×1ml	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$170.90
T113600-25ml	25ml	1	$320.90

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C-X (non halogen) bonding reaction (132) Element classified compounds (2014)

Basic Description

Synonyms	DTXSID70938225 \| Trimethylsulfoniumhydroxyd \| UNII-835839L58Y \| IODO-GLUTIONAL [WHO-DD] \| Trimethylsulfanium Hydroxide \| T1576 \| trimethylsulfanium;hydroxide \| 835839L58Y \| MFCD00216756 \| MDTPTXSNPBAUHX-UHFFFAOYSA-M \| Sulfonium, trimethyl-, hydroxide \| AI
Specifications & Purity	0.2mol/L in methanol
Storage Temp	Store at -20°C
Shipped In	Ice chest + Ice pads This product requires cold chain shipping. Ground and other economy services are not available.
Product Description	Trimethylsulfonium hydroxide (TMSH) is a methylating reagent. It can be prepared by dissolving trimethylsulfonium iodide in methanol and water solvent further treating with silver oxide.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Organic oxygen compounds
  - Class Organic oxoanionic compounds

Kingdom	Organic compounds
Superclass	Organic oxygen compounds
Class	Organic oxoanionic compounds
Subclass	Not available
Intermediate Tree Nodes	Not available
Direct Parent	Organic oxoanionic compounds
Alternative Parents	Organosulfur compounds Organic salts Organic oxides Hydrocarbon derivatives Organic cations
Molecular Framework	Aliphatic acyclic compounds
Substituents	Organic oxide - Hydrocarbon derivative - Organic salt - Organosulfur compound - Organic hydroxide - Organic cation - Aliphatic acyclic compound
Description	This compound belongs to the class of organic compounds known as organic oxoanionic compounds. These are organic compounds containing an oxoanion.
External Descriptors	Not available
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61. DOI: 10.1186/s13321-016-0174-y

Names and Identifiers

Pubchem Sid	504766009
Pubchem Sid Url	https://pubchem.ncbi.nlm.nih.gov/substance/504766009
IUPAC Name	trimethylsulfanium;hydroxide
INCHI	InChI=1S/C3H9S.H2O/c1-4(2)3;/h1-3H3;1H2/q+1;/p-1
InChIKey	MDTPTXSNPBAUHX-UHFFFAOYSA-M
Smiles	C[S+](C)C.[OH-]
Isomeric SMILES	C[S+](C)C.[OH-]
WGK Germany	2
PubChem CID	11105313
UN Number	3286
Molecular Weight	94.18
Beilstein	3910286
Reaxy-Rn	3910286

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

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

Analytical Chart:

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7 results found

Lot Number	Certificate Type	Date	Item
F2523190	Certificate of Analysis	Jun 21, 2022	T113600
G2228515	Certificate of Analysis	Jun 21, 2022	T113600
G2228513	Certificate of Analysis	Jun 21, 2022	T113600
G2228514	Certificate of Analysis	Jun 21, 2022	T113600
A2219114	Certificate of Analysis	Jan 06, 2022	T113600
A2219135	Certificate of Analysis	Jan 06, 2022	T113600
A2219136	Certificate of Analysis	Jan 06, 2022	T113600

Chemical and Physical Properties

Sensitivity	heat sensitive
Flash Point(°F)	11℃
Flash Point(°C)	11℃
Molecular Weight	94.180 g/mol
XLogP3
Hydrogen Bond Donor Count	1
Hydrogen Bond Acceptor Count	1
Rotatable Bond Count	0
Exact Mass	94.0452 Da
Monoisotopic Mass	94.0452 Da
Topological Polar Surface Area	2.000 Å²
Heavy Atom Count	5
Formal Charge	0
Complexity	8.000
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	2

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