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379212

Sigma-Aldrich

Hexamethyldisilazane

ReagentPlus®, 99.9%

Sinónimos:

1,1,1,3,3,3-Hexamethyldisilazane, HMDS

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About This Item

Fórmula lineal:
(CH3)3SiNHSi(CH3)3
Número de CAS:
999-97-3
Peso molecular:
161.39
Beilstein:
635752
Número CE:
213-668-5
Número MDL:
MFCD00008259
Código UNSPSC:
12352103
ID de la sustancia en PubChem:
24863226
NACRES:
NA.23

Línea del producto

ReagentPlus®

Ensayo

99.9%

Formulario

liquid

índice de refracción

n20/D 1.407 (lit.)

bp

125 °C (lit.)

cadena SMILES

C[Si](C)(C)N[Si](C)(C)C

InChI

1S/C6H19NSi2/c1-8(2,3)7-9(4,5)6/h7H,1-6H3

Clave InChI

FFUAGWLWBBFQJT-UHFFFAOYSA-N

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Descripción general

Hexamethyldisilazane (HDMS) is an organoslicon compound. HDMS is a colorless liquid used as a reagent and precursor in organic synthesis and organometallic chemistry. It is also used as a sol-gel precursor to fabricate thin films for semiconductor devices.

Aplicación

Hexamethyldisilazane can be used:
  • As a precursor to fabricate multilayer quantum dot light-emitting diodes.
  • To modify dielectric surfaces of organic thin film transistors.
  • To fabricate superhydrophobic coatings on epoxy resins.
  • For the silylation of alcohols and phenols.

Información legal

ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany

Pictogramas

FlameSkull and crossbones
GHS02,GHS06

Palabra de señalización

Danger

Clasificaciones de peligro

Acute Tox. 3 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Aquatic Chronic 3 - Flam. Liq. 2

Código de clase de almacenamiento

3 - Flammable liquids

Clase de riesgo para el agua (WGK)

WGK 2

Punto de inflamabilidad (°F)

52.5 °F - closed cup

Punto de inflamabilidad (°C)

11.4 °C - closed cup

Equipo de protección personal

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

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Certificados de análisis (COA)

Lot/Batch Number
SHBM6136
SHBJ6186
SHBH7587
SHBG6192V
SHBF8354V

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Si necesita una versión concreta, puede buscar un certificado específico por el número de lote.

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Clorotrimetilsilano ≥98.0% (GC)

Sigma-Aldrich

92361

Clorotrimetilsilano

Osmium tetroxide solution suitable for electron microscopy, 4% in H2O

Sigma-Aldrich

75632

Osmium tetroxide solution

Clorotrimetilsilano for GC derivatization, LiChropur™, ≥99.0% (GC)

Supelco

89595

Clorotrimetilsilano

G Chiavari et al.
Journal of chromatography. A, 922(1-2), 235-241 (2001-08-07)
Alpha-amino acids were pyrolysed at 600 degrees C in the presence of hexamethyldisilazane (HMDS) and the formed volatile products were analysed on line by gas chromatography-mass spectrometry (GC-MS). Glycine, alanine, valine, leucine, isoleucine, norleucine, methionine, phenylalanine yielded principally the trimethylsilyl
Joachim C Burbiel et al.
Beilstein journal of organic chemistry, 2, 20-20 (2006-10-28)
Poly-substituted xanthine derivatives are an important class of compounds in medicinal chemistry. Substitution at the 8-position of the purine ring is generally accessible by ring closure of a carboxamido-substituted uracil precursor. Although several procedures to accomplish this synthetic step have
D F Bray et al.
Microscopy research and technique, 26(6), 489-495 (1993-12-15)
Three different drying methods, critical-point drying (CPD), Peldri II, and hexamethyldisilazane (HMDS), were compared using representative animal (rat kidney, trachea, duodenum, lung, and red blood cells) and plant (leaves from ten species of monocotyledons and dicotyledons) specimens. All three drying
Greta M de Waal et al.
Scientific reports, 10(1), 8777-8777 (2020-05-31)
Gut dysbiosis contributes to the development of a dysfunctional gut barrier, facilitating the translocation of bacteria and inflammagens, and is implicated in colorectal cancer (CRC) pathogenesis. Such 'leaky gut' conditions result in systemic inflammation, of which a hallmark is increased
Else Driehuis et al.
Cancer discovery, 9(7), 852-871 (2019-05-06)
Previous studies have described that tumor organoids can capture the diversity of defined human carcinoma types. Here, we describe conditions for long-term culture of human mucosal organoids. Using this protocol, a panel of 31 head and neck squamous cell carcinoma
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