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Merck
CN

T0514

Trimethylamine N-oxide dihydrate

98%

Synonym(s):

TMANO

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About This Item

Linear Formula:
(CH3)3NO · 2H2O
CAS Number:
Molecular Weight:
111.14
EC Number:
214-675-6
UNSPSC Code:
12352116
PubChem Substance ID:
Beilstein/REAXYS Number:
3612927
MDL number:
Assay:
98%
Form:
powder
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Quality Level

assay

98%

form

powder

reaction suitability

reagent type: oxidant

mp

95-99 °C (lit.)

SMILES string

O.O.C[N+](C)(C)[O-]

InChI

1S/C3H9NO.2H2O/c1-4(2,3)5;;/h1-3H3;2*1H2

InChI key

PGFPZGKEDZGJQZ-UHFFFAOYSA-N

Application

Trimethylamine N-oxide dihydrate can be used as:
  • A decarbonylating agent in many chemical reactions.
  • An oxidizing agent for organoboranes.
  • A standard in the determination of amines in air samples using non-suppressed ion chromatography.

Reactant for:
  • C-H bond cleavage
  • Oxidation reactions (oxidant)

  • Decarbonylating agent for solvent-free reactions


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pictograms

Exclamation mark

signalword

Warning

hcodes

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2

Storage Class

11 - Combustible Solids

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves



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Electrophilic attack on diphosphazane-bridged derivatives of diruthenium nonacarbonyl by halogens. Crystal structure of [Ru2 ({′A}-I) I (CO)3 {{′A}-(PriO)2 PN (Et)P (OPri)2}2]
John S, et al.
J. Chem. Soc., Dalton Trans., 10, 2761-2768 (1991)
Oxidation of organoboranes with trimethylamine N-oxide dihydrate
Kabalka GW
Journal of Organometallic Chemistry, 125(2), 273-280 (1977)
Hui Wei et al.
Frontiers in microbiology, 9, 3276-3276 (2019-01-29)
Yarrowia lipolytica, known to accumulate lipids intracellularly, lacks the cellulolytic enzymes needed to break down solid biomass directly. This study aimed to evaluate the potential metabolic burden of expressing core cellulolytic enzymes in an engineered high lipid-accumulating strain of Y.



Global Trade Item Number

SKUGTIN
T0514-100G04061833554098