JavaScript seems to be disabled in your browser. For the best experience on our site, be sure to turn on Javascript in your browser.

This is a demo store. No orders will be fulfilled.

Account

Settings

Language

྾

Home
Chemistry & Biochemicals
Chemical Synthesis
Ionic Liquids
Tetramethylammonium iodide - 98%, high purity , CAS No.75-58-1

Skip to the end of the images gallery

Skip to the beginning of the images gallery

Tetramethylammonium iodide - 98%, high purity , CAS No.75-58-1

4 Citations

COA

Grade & Purity:

≥98%

Cas Number: 75-58-1
Molecular Weight: 201.05
Beilstein Registry Number: 3620030
EC Number: 200-881-3
MDL number: MFCD00011629
PubChem CID: 6381

In stock

Item Number

T100317

Grouped product items
SKU	Size	Availability	Price
T100317-5g	5g	1	$9.90
T100317-25g	25g	2	$28.90
T100317-100g	100g	1	$88.90
T100317-500g	500g	Available within 4-8 weeks(?) Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!	$339.90

View related series

Ammonium salt capping agent (44) Biochemical Assay Reagents (928) phase transfer catalyst (106)

Basic Description

Synonyms	HY-W014861 \| Q26840810 \| AKOS015833289 \| T0139 \| Yodurtan \| EINECS 200-881-3 \| Banikol \| SCHEMBL108581 \| F87494 \| TMAI \| Tetramethyl ammonium iodide \| UNII-L493Z502W3 \| TRETRAMETHYLAMMONIUM IODIDE \| ghl.PD_Mitscher_leg0.944 \| RXMRGBVLCSYIBO-UHFFFAOYSA-M \|
Specifications & Purity	≥98%
Storage Temp	Protected from light,Room temperature
Shipped In	Normal

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Organic nitrogen compounds
  - Class Organonitrogen compounds
    - Subclass Quaternary ammonium salts

Kingdom	Organic compounds
Superclass	Organic nitrogen compounds
Class	Organonitrogen compounds
Subclass	Quaternary ammonium salts
Intermediate Tree Nodes	Not available
Direct Parent	Tetraalkylammonium salts
Alternative Parents	Organopnictogen compounds Organic iodide salts Hydrocarbon derivatives Amines
Molecular Framework	Aliphatic acyclic compounds
Substituents	Tetraalkylammonium salt - Organopnictogen compound - Hydrocarbon derivative - Organic iodide salt - Organic salt - Amine - Aliphatic acyclic compound
Description	This compound belongs to the class of organic compounds known as tetraalkylammonium salts. These are organonitrogen compounds containing a quaternary ammonium substituted with four alkyl chains.
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

Associated Targets(Human)

CHRNA1 Tclin Acetylcholine receptor protein alpha chain (98 Activities)

Discover Target: CHRNA1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

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	tetramethylazanium;iodide
INCHI	InChI=1S/C4H12N.HI/c1-5(2,3)4;/h1-4H3;1H/q+1;/p-1
InChIKey	RXMRGBVLCSYIBO-UHFFFAOYSA-M
Smiles	C[N+](C)(C)C.[I-]
Isomeric SMILES	C[N+](C)(C)C.[I-]
WGK Germany	3
RTECS	PA1050000
PubChem CID	6381
UN Number	2811
Molecular Weight	201.05
Beilstein	3620030
Reaxy-Rn	3620030

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.

19 results found

Lot Number	Certificate Type	Date	Item
C2507619	Certificate of Analysis	Feb 22, 2025	T100317
C2507626	Certificate of Analysis	Feb 22, 2025	T100317
C2507636	Certificate of Analysis	Feb 22, 2025	T100317
C2507646	Certificate of Analysis	Feb 22, 2025	T100317
C2507635	Certificate of Analysis	Feb 22, 2025	T100317
E2516077	Certificate of Analysis	Feb 22, 2025	T100317
K2218079	Certificate of Analysis	Feb 17, 2025	T100317
A2515117	Certificate of Analysis	Jul 31, 2024	T100317
H2409635	Certificate of Analysis	Jul 31, 2024	T100317
H2409636	Certificate of Analysis	Jul 31, 2024	T100317
H2409615	Certificate of Analysis	Jul 31, 2024	T100317
H2409616	Certificate of Analysis	Jul 31, 2024	T100317
H2409637	Certificate of Analysis	Jul 31, 2024	T100317
H2409638	Certificate of Analysis	Jul 31, 2024	T100317
E2406210	Certificate of Analysis	Mar 25, 2024	T100317
E2406224	Certificate of Analysis	Mar 25, 2024	T100317
A2219374	Certificate of Analysis	Oct 11, 2023	T100317
A2219412	Certificate of Analysis	Oct 11, 2023	T100317
A2219418	Certificate of Analysis	Oct 11, 2023	T100317

Show more⌵

Chemical and Physical Properties

Solubility	Slightly soluble in water. Insoluble in chloroform, ether
Sensitivity	Moisture & Light sensitive
Melt Point(°C)	>300°C
Molecular Weight	201.050 g/mol
XLogP3
Hydrogen Bond Donor Count	0
Hydrogen Bond Acceptor Count	1
Rotatable Bond Count	0
Exact Mass	201.001 Da
Monoisotopic Mass	201.001 Da
Topological Polar Surface Area	0.000 Å²
Heavy Atom Count	6
Formal Charge	0
Complexity	19.100
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

Citations of This Product

How to Cite Aladdin Scientific Products?

1. Qi Li, Yi-lei Li, Bo Li, Ying-juan Hao, Xiao-jing Wang, Rui-hong Liu, Yuan Ling, Xinying Liu, Fa-tang Li. (2021) Construction of adjustable dominant {314} facet of Bi5O7I and facet-oxygen vacancy coupling dependent adsorption and photocatalytic activity. APPLIED CATALYSIS B-ENVIRONMENTAL, 289 (120041).
2. Xuejiang Cheng, Xin Wang, Guangming Chen. (2018) A convenient and highly tunable way to n-type carbon nanotube thermoelectric composite film using common alkylammonium cationic surfactant. Journal of Materials Chemistry A, 6 (39): (19030-19037).
3. Yingli Wang, Jialong Duan, Yuanyuan Zhao, Benlin He, Zhengbo Jiao, Qunwei Tang. (2018) Hybridized dye-sensitized solar cells for persistent power generation free of sun illumination. ELECTROCHIMICA ACTA, 280 (181).
4. Wen-Wang Yu, Xiang-Guang Meng, Wen Li, Li-Yu Chen, Zi-Yu Gan, Yu-Lian Zhang, Jie Zhou. (2024) Highly efficient capture and conversion of CO2 into cyclic carbonates from actual flue gas under atmospheric pressure. Journal of Environmental Chemical Engineering, 12 (113614).

Solution Calculators

Molarity Calculator

Determine the necessary mass, volume, or concentration for preparing a solution.

Mass

Concentration

Volume

M. Wt*

g/mol

*When preparing stock solutions, always use the batch-specific molecular weight of the product found on the vial label and the Certificate of Analysis (available online).

Dilution Calculator

Determine the dilution needed to prepare a stock solution.

Concentration 1 (C1)

Volume 1 (V1)

Concentration 2 (C2)

Volume 2 (V2)

Reconstitution Calculator

The reconstitution calculator enables you to quickly determine the volume of a reagent needed to reconstitute your vial. Just enter the mass of the reagent and the target concentration, and the calculator will do the rest.

Volume (to add to vial)

Mass (in vial)

Desired Reconstitution Concentration

Reviews

Shall we send you a message when we have discounts available?

Remind me later

Thank you! Please check your email inbox to confirm.

Oops! Notifications are disabled.