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15236

Sigma-Aldrich

N,O-Bis(trimethylsilyl)carbamate

≥98.0% (T)

Synonym(s):

BSC, Trimethylsilyl N-(trimethylsilyl)carbamate

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$82.60

About This Item

Linear Formula:
(CH3)3SiNHCO2Si(CH3)3
CAS Number:
35342-88-2
Molecular Weight:
205.40
Beilstein/REAXYS Number:
2043399
EC Number:
252-520-4
MDL number:
MFCD00040476
UNSPSC Code:
12352100
PubChem Substance ID:
329750791
NACRES:
NA.22

$82.60

List Price$118.00Save 30%
Web-Only Promotion

Available to ship onApril 29, 2025Details

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Quality Level

100

assay

≥98.0% (T)

form

solid

mp

77-83 °C

functional group

amine

SMILES string

C[Si](C)(C)NC(=O)O[Si](C)(C)C

InChI

1S/C7H19NO2Si2/c1-11(2,3)8-7(9)10-12(4,5)6/h1-6H3,(H,8,9)

InChI key

DGIJAZGPLFOQJE-UHFFFAOYSA-N

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Other Notes

Extremely suitable reagent for the silylation of alcohols, phenols and carboxylic acids. The only by-products are CO2 and NH3[1]; Silyloxycarbonylation of amines[2][3]; Acylisocyanates from carboxylic acid chlorides[4]

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
048627/1
048627/1V

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Zhur. Obshch. Khim., 50, 955-955 (1980)
V.P. Kozyukov et al.
Zhur. Obshch. Khim., 51, 239-239 (1981)
V.P. Kozyukov et al.
Current Chemical Reactions, 2, 6251-6251 (1980)
Isabelle C Arnold et al.
The Journal of experimental medicine, 215(8), 2055-2072 (2018-07-05)
Eosinophils are predominantly known for their contribution to allergy. Here, we have examined the function and regulation of gastrointestinal eosinophils in the steady-state and during infection with Helicobacter pylori or Citrobacter rodentium We find that eosinophils are recruited to sites
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