Product Overview
Trimethylamine N-oxide dihydrate (TMAO, C₃H₉NO·2H₂O, CAS 62637-93-8) is a small, zwitterionic amine oxide supplied as a white, freely water-soluble crystalline dihydrate. In the laboratory sciences it serves three core non-medical roles: (1) as the classic chemical chaperone and compatible osmolyte that stabilizes proteins against urea, heat, pressure and ice denaturation in biochemical research; (2) as a mild, selective oxidant and oxygen-transfer reagent in organic synthesis; and (3) as a reagent in functional-materials preparation, cryopreservation research and analytical chemistry.
Core value propositions:
Mild Organic Oxidant:
● selective oxidation of iodides, thiols, phosphines; oxygen donor in metal catalysis;
Functional-Materials Reagent:
● synthesis of thermally stable TiO₂-nanorod polymers and semiconductor/metal nanocomposites;
Stable, High-Solubility Form:
● dihydrate is the standard shelf-stable commercial form, freely soluble in water.
Product Information (Quick Facts)
Item | Specification |
Chemical Name | Trimethylamine N-oxide dihydrate (TMAO dihydrate; 2-hydrate) |
Synonyms | TMAO; TMO; TMANO; trimethylamine oxide dihydrate; N,N-dimethylmethanamine N-oxide dihydrate |
CAS No. | 62637-93-8 (commercial reference); 62637-93-4 (standard registry number) — both refer to the same product |
EC No. (EINECS) | 214-675-6 |
Molecular Formula | C₃H₉NO·2H₂O (C₃H₁₃NO₃) |
Molecular Weight | 111.14 g/mol (dihydrate); 75.11 g/mol (anhydrous, CAS 1184-78-7) |
Appearance | White to off-white fine crystalline powder (moisture-sensitive) |
Melting Point | ≈ 95–99 °C (lit.); anhydrous form 220–222 °C |
Solubility | Soluble in water, ethanol, DMSO and methanol; sparingly soluble in hot chloroform; insoluble in ether, benzene and hydrocarbons |
Assay | ≥ 99 % |
Chemistry & Structure
TMAO is the N-oxide of trimethylamine: a nitrogen atom bonded to three methyl groups and an oxide oxygen, (CH₃)₃N⁺–O⁻, isolated commercially as the dihydrate. It is a highly polar, zwitterionic molecule with excellent solubility in water, ethanol, DMSO and methanol, and very low acute toxicity. The dihydrate melts around 95–99 °C; the anhydrous form melts at 220–222 °C. Because it is moisture-sensitive and hygroscopic, the dihydrate is the preferred shelf-stable commercial form. In aqueous solution TMAO behaves as a compatible osmolyte: As an oxidant, its N–O bond readily transfers oxygen to soft reducing centers (iodide, thiols, phosphines) and to transition-metal complexes.
Key Features & Benefits
● Mild, selective oxidant: clean oxygen transfer with mild conditions and easy work-up.
● Excellent solubility: freely soluble in water, ethanol, DMSO and methanol — easy buffer and stock preparation.
● Stable dihydrate form: shelf-stable, economical alternative to the hygroscopic anhydrous material.
● Broad utility: biochemistry, synthesis, materials and analytical use.
● Reliable quality: controlled assay, water content and purity; COA with every batch.
Main Applications
1 Biochemistry Research
● Marine biology: mechanism studies of the deep-sea osmolyte TMAO counteracting pressure/urea denaturation;
● Structural biology: stabilizing additive in protein preparation, purification and crystallization.
2 Organic Synthesis Oxidant & Oxygen-Transfer Reagent
● Mild oxidations: iodide to iodine, thiols to disulfides, phosphines to phosphine oxides;
● Metal-catalyzed oxidations: oxygen donor in heterometallic-cluster and Mo/Cu-mediated oxidation and hydrogenation chemistry;
● Process chemistry: safe, water-soluble alternative to peroxide-based oxidants in sensitive substrates;
● Synthetic transformations: N-oxide chemistry and oxidative coupling applications.
3 Functional Materials & Nanocomposite Synthesis
● Polymer composites: preparation of thermally stable TiO₂-nanorod incorporated polymers;
● Nanocomposites: semiconductor/metal nanocomposite synthesis where TMAO acts as oxidant/oxygen-transfer agent;
● Catalyst preparation: reagent in the synthesis of oxidation and cluster catalysts;
● Materials R&D: controlled-chemistry routes to metal-oxide and hybrid materials.
4 Analytical & Laboratory Reagent
● Laboratory reagent: standard TMAO source for analytical and synthetic work;
● Reference material: internal standards for NMR, MS and LC method development;
● Education and research: teaching and biochemistry lab use in universities and institutes;
● Quality control: routine reagent applications in industrial and contract laboratories.
Packaging, Storage
Packaging (customizable):
● 25 g / 100 g / 500 g / 1 kg laboratory bottles; 25 kg fiber drums for production scale;
Storage:
● Store in a cool, dry, well-ventilated area; keep containers tightly closed (sealed in dry, room temperature);
● Protect from moisture and humidity; keep away from strong oxidizers and acids;
● Avoid inhaling dust; use local ventilation when handling large quantities.
Why Choose Jinan Future Chemical Co., Ltd.?
● Factory-direct supply: own production and sourcing capability, transparent pricing;
● Stable quality: strict internal control, every batch tested (assay ≥ 99%, water content, purity), COA with every shipment;
● Export experience: smooth air and sea shipping worldwide,
FAQ
Q1: What are the uses of trimethylamine N-oxide (TMAO) dihydrate?
TMAO dihydrate is used: (1) in biochemical research as a chemical chaperone and compatible osmolyte,structural biology and marine-biology research; (2) in organic synthesis as a mild, selective oxidant — oxidizing iodides to iodine, thiols to disulfides and phosphines to phosphine oxides, and serving as an oxygen donor in transition-metal-catalyzed oxidations; (3) in functional-materials research for the synthesis of thermally stable TiO₂-nanorod polymers and semiconductor/metal nanocomposites; (4) as an analytical and laboratory reagent.
Q2: Why is TMAO such an effective protein stabilizer?
TMAO is preferentially excluded from the protein surface in aqueous solution: it is pushed away from the peptide backbone, which raises the free-energy cost of an unfolded, surface-exposed conformation and therefore thermodynamically favors the compact native state. This 'preferential exclusion' mechanism is why TMAO counteracts chaotropes such as urea and guanidinium chloride, and why deep-sea organisms accumulate TMAO to offset the denaturing effects of high hydrostatic pressure. It is the textbook example of a compatible osmolyte and chemical chaperone.