Triisopropylsilane

Triisopropylsilane
Names
	Preferred IUPAC name Tri(propan-2-yl)silane
	Other names TIS or TIPS
Identifiers
CAS Number	6485-79-6;
3D model (JSmol)	Interactive image;
ChemSpider	122362;
ECHA InfoCard	100.104.805
EC Number	464-880-1;
PubChem CID	6327611;
CompTox Dashboard (EPA)	DTXSID90983439 ;
	InChI InChI=1S/C9H21Si/c1-7(2)10(8(3)4)9(5)6/h7-9H,1-6H3 Key: ZGYICYBLPGRURT-UHFFFAOYSA-N;
	SMILES CC(C)[Si](C(C)C)C(C)C;
Properties
Chemical formula	C9H22Si
Molar mass	158.360 g·mol−1
Density	0.773 g/mL
Boiling point	166 °C (331 °F; 439 K)
Hazards
	GHS labelling:
Pictograms
Signal word	Warning
Hazard statements	H226, H315, H317, H319, H335
Precautionary statements	P210, P233, P240, P241, P242, P243, P261, P264, P271, P272, P280, P302+P352, P303+P361+P353, P304+P340, P305+P351+P338, P312, P321, P332+P313, P333+P313, P337+P313, P362, P363, P370+P378, P403+P233, P403+P235, P405, P501
Flash point	35 °C
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references

Triisopropyl silane (TIPS) is an organosilicon compound with the formula (i-Pr)₃SiH (i-Pr = isopropyl). This colorless liquid is used as a scavenger in peptide synthesis. It can also act as a mild reducing agent.

In peptide synthesis, TIPS is used as a scavenger for peptide groups being removed from the peptide sequence at the global deprotection. TIPS is able to scavenge carbocations formed in the deprotection of a peptide as it can act as a hydride donor in acidic conditions.^[1] Silanes may be preferred as scavengers in place of sulfur-based scavengers.

^ Pearson, Daniel A.; Blanchette, Mary; Baker, Mary Lou; Guindon, Cathy A. (1989). "Trialkylsilanes as scavengers for the trifluoroacetic acid deblocking of protecting groups in peptide synthesis". Tetrahedron Letters. 30 (21): 2739–2742. doi:10.1016/s0040-4039(00)99113-5.

[1] Pearson, Daniel A.; Blanchette, Mary; Baker, Mary Lou; Guindon, Cathy A. (1989). "Trialkylsilanes as scavengers for the trifluoroacetic acid deblocking of protecting groups in peptide synthesis". Tetrahedron Letters. 30 (21): 2739–2742. doi:10.1016/s0040-4039(00)99113-5.

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