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Merck

52619

Supelco

Hexamethyldisilazane

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

Sinónimos:

HMDS

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About This Item

Fórmula lineal:
(CH3)3SiNHSi(CH3)3
Número de CAS:
Peso molecular:
161.39
Beilstein:
635752
Número CE:
Número MDL:
Código UNSPSC:
12000000
ID de la sustancia en PubChem:
NACRES:
NA.22

grado

for GC derivatization

Nivel de calidad

Análisis

≥99.0% (GC)

formulario

liquid

calidad

LiChropur

idoneidad de la reacción

reagent type: derivatization reagent
reaction type: Silylations

técnicas

gas chromatography (GC): suitable

índice de refracción

n20/D 1.407 (lit.)
n20/D 1.408

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 (HMDS) is a commercially available, silylating agent, which is used as an alternative for the preparation of silyl ethers from hydroxyl compounds.

Aplicación

Learn more in the Product Information
Hexamethyldisilazane is suitable for the derivatization of alcohols, U-aminobutyric acid, pesticidal carbamates and urea, 3,4-Dihydroxyphenylglycol, 4-hydroxycoumarins, hydroxyfatty acids, n-hydroxy-2-fluorenylacetamide, kerb cycle acid, malonaldehyde, monoglycerides, phenylpyruvic acid, shikimic acid, unsaturated fatty acid esters (or methyl esters), and related compounds.

It may be used as a derivatizing reagent for the analysis of bioamines and their acidic metabolites, phenol, hydroquinone and catechol in urine samples, mixtures of free fatty acids and metal soaps in paint samples using gas chromatography/mass spectrometry (GC/MS).
Suitable for the derivatization of alcohols, Υ-aminobutyric acid, pesticidal carbamates and urea, 3,4-Dihydroxyphenylglycol, 4-hydroxycoumarins, hydroxyfatty acids, n-hydroxy-2-fluorenylacetamide, kerb cycle acid, malonaldehyde, monoglycerides, phenylpyruvic acid, shikimic acid, unsaturated fatty acid esters (or methyl esters), and related compounds.

Características y beneficios

  • HMDS is inexpensive and has a relatively low boiling point (124-127 °C).        
  • It can be used without solvent but its silylating power can be increased by various (mostly acidic) catalysts.        
  • The only reaction byproduct, ammonia, can leave the reaction mixture as the reaction goes to completion.

Otras notas

Importante agente sililante
Reagent for 2-hydroxypyrimidine, polytrimethylsilyloxy, trimethylsilyl and trimethylsilyl oximes.

Información legal

LiChropur is a trademark of Merck KGaA, Darmstadt, Germany

Pictogramas

FlameSkull and crossbones

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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Visite la Librería de documentos

Comprehensive profiling analysis of bioamines and their acidic metabolites in human urine by gas chromatography/mass spectrometry combined with selective derivatization
Park H-N, et al.
Journal of Chromatography A, 1305, 234-243 (2013)
J. Heberle et al.
Silylating Agents, 2nd ed. (1995)
Tania Limongi et al.
Biomedical materials (Bristol, England) (2020-11-14)
Generation of artifical vascular grafts (TEVG) as blood vessel substitutes is a primary challenge in biomaterial and tissue engineering research. Ideally, these grafts should be able to recapitulate physiological and mechanical properties of natural vessels and guide the assembly of
Oxide-based Systems at the Crossroads of Chemistry (2001)
Jacopo La Nasa et al.
Analytica chimica acta, 1001, 51-58 (2018-01-03)
In this paper we present a new analytical GC/MS method for the analysis of mixtures of free fatty acids and metal soaps in paint samples. This approach is based on the use of two different silylating agents: N,O-bis(trimethylsilyl)trifluoroacetamide (BSTFA) and

Artículos

Results of a study involving the ability few Fluka silylating reagents to form GC-MS-compatible trimethylsilylmethyl derivatives of NSAIDs

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