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
Beilstein:
3612927
EC Number:
MDL number:
UNSPSC Code:
12352116
PubChem Substance ID:
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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
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Related Categories
Application
Reactant for:
- C-H bond cleavage
- Oxidation reactions (oxidant)
- Decarbonylating agent for solvent-free reactions
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.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2
Storage Class Code
11 - Combustible Solids
WGK
WGK 2
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
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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)
Thermal degradation of transition metal carbonyl complexes: Part IV: Thermogravimetric studies of various stoichiometric mixtures of trimethylamine N-oxide dihydrate and hexacarbonyl molybdenum
Chan HSO, et al.
Thermochimica Acta, 145, 179-187 (1989)
Mark E Erupe et al.
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An ion chromatography method with non-suppressed conductivity detection was developed for the simultaneous determination of methylamines (methylamine, dimethylamine, trimethylamine) and trimethylamine-N-oxide in particulate matter air samples. The analytes were well separated by means of cation-exchange chromatography using a 3 mM
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