Trimethylsilylmethyl-Triphenylphosphonium Iodide

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MOQ : 10 Kilograms

Trimethylsilylmethyl-Triphenylphosphonium Iodide Specification

Melting Point
230-232C (decomposes)

Storage
Store in cool, dry place, under inert atmosphere, tightly closed

Grade
Analytical Grade / Research Grade

Smell
Odorless

Molecular Weight
478.43 g/mol

Solubility
Soluble in polar aprotic solvents (e.g., DMSO, DMF, acetonitrile); slight solubility in water

Ingredients
Trimethylsilylmethyl-Triphenylphosphonium Iodide

HS Code
29319090

Molecular Formula
C22H28IPSi

Properties
Moisture sensitive, Air sensitive, Stable under recommended conditions, Non-flammable

Application
Organic synthesis, particularly for the introduction of trimethylsilylmethyl groups

EINECS No
241-654-0

Usage
Used as a reagent in Wittig-type reactions and related organophosphorus transformations

Structural Formula
[Ph3P+CH2SiMe3]I-

Poisonous
NO

Shape
Crystalline

Appearance
White to off-white crystalline powder

CAS No
17670-82-7

Product Type
Phosphonium Salt

Purity
>98%

Shelf Life
12-24 months if properly stored

Physical Form
Solid (Powder or Crystals)

Boiling Point
Decomposes before boiling

Sensitivity
Sensitive to air and moisture

UN Number
Non-regulated

Synonyms
(Trimethylsilyl)methyltriphenylphosphonium iodide; Phosphonium, [(trimethylsilyl)methyl]triphenyl-, iodide

Packaging
Sealed bottles under inert gas, commonly available in 1g, 5g, 25g quantities

Handling Precautions
Use in glove box or under dry nitrogen/argon atmosphere

Hazard Class
Not classified as hazardous under GHS

EC Number
241-654-0

Decomposition Temperature
Above 230C

About Trimethylsilylmethyl-Triphenylphosphonium Iodide

Discover the must-have, new Trimethylsilylmethyl-Triphenylphosphonium Iodide-an impeccable addition for any advanced organic synthesis lab. This sought-after reagent, also known as (Trimethylsilyl)methyltriphenylphosphonium iodide, boasts blue-ribbon purity (>98%) and is perfect for Wittig-type reactions and organophosphorus transformations. Stable and non-flammable, it arrives in sealed bottles filled under inert gas to preserve quality. With a white crystalline appearance and odorless nature, it is available in 1g, 5g, and 25g quantities. Get it now from your trusted supplier in India-unparalleled performance guaranteed.

Versatile Applications and Ideal Suitability

Trimethylsilylmethyl-Triphenylphosphonium Iodide is suitable for use in university labs, chemical research institutes, and industrial R&D centers. Its primary application is in organic synthesis, especially for introducing trimethylsilylmethyl groups through Wittig-type or organophosphorus reactions. This reagent is optimal for laboratories focusing on advanced synthetic methodologies, enabling high-yield and selective transformations. It is a favored choice among chemists striving for precision and reliability in their site-specific functional group installations.

Payment Terms, Packaging, and Sample Policies

The asking price for Trimethylsilylmethyl-Triphenylphosphonium Iodide is available on request, with favorable terms for the domestic market. Packaging details include secure, sealed bottles under inert gas, commonly handed over in quantities of 1g, 5g, or 25g to ensure integrity and ease of transport. Sample policy typically allows qualified buyers to request small test portions for evaluation, making it convenient to assess suitability before a larger commitment.

FAQ's of Trimethylsilylmethyl-Triphenylphosphonium Iodide:

Q: How should Trimethylsilylmethyl-Triphenylphosphonium Iodide be handled safely?

A: It should be manipulated in a glove box or under a dry nitrogen or argon atmosphere due to its high sensitivity to air and moisture.

Q: What is the primary usage of this chemical?

A: It is mainly used as a reagent in Wittig-type reactions and various organophosphorus transformations in organic synthesis.

Q: Where can this reagent be applied effectively?

A: Ideal application sites include research laboratories, industrial R&D departments, and academic institutions engaging in advanced organic synthesis.