≥95% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping
Store at 2-8°C Ships Wet ice Check lot-specific COA for exact specifications.
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Quality documents
SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
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Literature proof
Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Overview
Description
When used with aliphatic or aromatic aldehydes, this silicon amine protocolSLAP reagent enables the photomediated synthesis of thiomorpholines and thiazepanes. For photocatalytic cross-coupling with this SLAP Reagent, Ir[(ppy)2dtbbpy]PF6(747769) is used with a recommended starting combination of Lewis acids Bi(OTf)3(633305) and Cu(OTf)2(283673) prior to subsequent substrate-specific optimization. This product was introduced in collaboration with theBode Research Groupand provides a tin-free alternative toSnAP(tin amine protocol) reagents and is well-suited for scale-up reactions.
Specifications
Synonyms
3-(((Trimethylsilyl)methyl)thio)propan-1-amine
Specifications & Purity
≥95%
Storage
Store at 2-8°C
Shipped In
Wet ice
This product requires cold chain shipping. Ground and other economy services are not available.
Purity
≥95%
Names and Identifiers
Canonical Smiles
C[Si](C)(C)CSCCCN
IUPAC Name
3-(trimethylsilylmethylsulfanyl)propan-1-amine
InChIKey
CNESDLLESCAVSR-UHFFFAOYSA-N
INCHI
1S/C7H19NSSi/c1-10(2,3)7-9-6-4-5-8/h4-8H2,1-3H3
PubChem CID
131801567
UN Number
1993C
Molecular Weight
177.38
Documentation
📋 Safety Data Sheet (SDS)
Comprehensive hazard, handling, storage, and regulatory compliance document.
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