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291013

Sigma-Aldrich

Chlorotriisobutylsilane

97%

Synonym(s):

Triisobutylchlorosilane, Triisobutylsilyl chloride

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5 G
€154.00

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5 G
€154.00

About This Item

Linear Formula:
[(CH3)2CHCH2]3SiCl
CAS Number:
13154-25-1
Molecular Weight:
234.88
Beilstein:
2409275
EC Number:
454-150-0
MDL number:
MFCD00010658
UNSPSC Code:
12352001
PubChem Substance ID:
24857505
NACRES:
NA.22

€154.00

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Quality Level

100

Assay

97%

refractive index

n20/D 1.448 (lit.)

density

0.875 g/mL at 25 °C (lit.)

SMILES string

CC(C)C[Si](Cl)(CC(C)C)CC(C)C

InChI

1S/C12H27ClSi/c1-10(2)7-14(13,8-11(3)4)9-12(5)6/h10-12H,7-9H2,1-6H3

InChI key

TZPZCTBZJKZFGY-UHFFFAOYSA-N

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Application

Chlorotriisobutylsilane can be used as an intermediate in the synthesis of:
  • Silicon (IV) phthalocyanines, which are used as photosensitizers for the photodynamic inactivation of bacteria.[1]
  • Poly(4-alkylthiazole) polymers exhibiting optical and electronic properties.[2]
  • Bis(trialkylsilyl oxide) based silicon phthalocyanines applicable as ternary additives in organic photovoltaics.[3]

Pictograms

Corrosion
GHS05

Signal Word

Danger

Hazard Statements

H314

Hazard Classifications

Skin Corr. 1B

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 3

Flash Point(F)

188.6 °F - closed cup

Flash Point(C)

87 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
0000179416
SHBP7688
SHBN9849
SHBN8536
SHBK2081

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Bis (trialkylsilyl oxide) Silicon Phthalocyanines: Understanding the Role of Solubility in Device Performance as Ternary Additives in Organic Photovoltaics
Vebber MC, et al.
Langmuir, 36(10), 2612-2621 (2020)
Octacationic and axially di-substituted silicon (IV) phthalocyanines for photodynamic inactivation of bacteria
van de Winckel E, et al.
Dyes and Pigments, 145, 239-245 (2017)
Toward n-type analogues to poly (3-alkylthiophene) s: influence of side-chain variation on bulk-morphology and electron transport characteristics of head-to-tail regioregular poly (4-alkylthiazole) s
Jager J, et al.
Journal of Material Chemistry C, 4(13), 2587-2597 (2016)

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