An amine oxide, also known as amine-N-oxide and N-oxide, is a chemical compound that contains the functional group R3N+−O−, an N−O coordinate covalent bond with three additional hydrogen and/or hydrocarbon side chains attached to N. Sometimes it is written as R3N→O or, wrongly, as R3N=O.
In the strict sense the term amine oxide applies only to oxides of tertiary amines. Sometimes it is also used for the analogous derivatives of primary and secondary amines.
Amine oxides are surfactants commonly used in consumer products such as shampoos, conditioners, detergents, and hard surface cleaners. Alkyl dimethyl amine oxide (chain lengths C10–C16) is the most commercially used amine oxide. They are considered a high production volume class of compounds in more than one member country of the Organisation for Economic Co-operation and Development (OECD); with annual production over 26,000, 16,000 and 6,800 metric tons in the US, Europe, and Japan, respectively. In North America, more than 95% of amine oxides are used in home cleaning products. They serve as stabilizers, thickeners, emollients, emulsifiers and conditioners with active concentrations in the range of 0.1–10%. The remainder (< 5%) is used in personal care, institutional, commercial products and for unique patented uses such as photography.
Amine oxides are highly polar molecules and have a polarity close to that of quaternary ammonium salts. Small amine oxides are very hydrophilic and have an excellent water solubility and a very poor solubility in most organic solvents.
- Pyrolytic elimination. Amine oxides, when heated to 150–200 °C eliminate a hydroxylamine, resulting in an alkene. This pyrolytic syn-elimination reaction is known under the name Cope reaction. The mechanism is similar to that of the Hofmann elimination.
- Reduction to amines. Amine oxides are readily converted to the parent amine by common reduction reagents including lithium aluminium hydride, sodium borohydride, catalytic reduction, zinc / acetic acid, and iron / acetic acid. Pyridine N-oxides can be deoxygenated by phosphorus oxychloride
- Sacrificial catalysis. Oxidants can be regenerated by reduction of N-oxides, as in the case of regeneration of osmium tetroxide by N-methylmorpholine oxide.
- O-alkylation. Pyridine N-oxides react with alkyl halides to the O-alkylated product
- Bis-ter-pyridine derivatives adsorbed on silver surfaces are discussed to react with oxygen to bis-ter-pyridine-N-oxide. This reaction can be followed by video-scanning tunneling microscopy with sub-molecular resolution.
- In the Meisenheimer rearrangement (after Jakob Meisenheimer) certain N-oxides R1R2R3N+O− rearrange to hydroxylamines R2R3N−O−R1
- In the Polonovski reaction a tertiary N-oxide is cleaved by acetic acid anhydride to the corresponding acetamide and aldehyde:
|1643-20-5||1-Dodecanamine, N,N-dimethyl-, N-oxide (C12 AO)|
|3332-27-2||1-Tetradecanamine, N,N-dimethyl-, N-oxide (C14 AO)|
|70592-80-2||Amines, C10-16-alkyldimethyl, N-oxides (C10-16 AO)|
|68955-55-5||Amines, C12-18-alkyldimethyl, N-oxides (C12-18 AO)|
|2605-79-0||Decanamine, N,N-dimethyl-, N-oxide|
|7128-91-8||Hexadecanamine, N,N-dimethyl-, N-oxide|
|2571-88-2||Octadecanamine, N,N-dimethyl-, N-oxide|
|61788-90-7||Amine oxides, cocoalkyldimethyl|
|85408-48-6||Amines, C10-18-alkyldimethyl, N-oxides|
|85408-49-7||Amines, C12-16-alkyldimethyl, N-oxides|
|61791-47-7||Ethanol, 2,2'-iminobis-, N-coco alkyl derivs., N-oxides|
|61791-46-6||Ethanol, 2,2'-iminobis-, N-tallow alkyl derivs., N-oxides|
Amine oxides (AO) are not known to be carcinogenic, dermal sensitizers or cause reproductive toxicity. They are readily metabolized and excreted if ingested. Chronic ingestion by rabbits found lower body weight, diarrhea and lenticular opacities at a lowest observed adverse effect levels (LOAEL) in the range of 87–150 mg AO/kw bw/day. Tests of human skin exposure have found that after 8 hours less than 1% is absorbed into the body. Eye irritation due to amine oxides and other surfactants is moderate and temporary with no lasting effects.
Amine oxides with an average chain length of 12.6 have been measured to be water-soluble at ~410 g L−1. They are considered to have low bioaccumulation potential in aquatic species based on log Kow data from chain lengths less than C14 (bioconcentration factor < 87%). Levels of AO in untreated influent were found to be 2.3–27.8 ug L−1, while in effluent they were found to be 0.4–2.91 ug L−1. The highest effluent concentrations were found in oxidation ditch and trickling filter treatment plants. On average, over 96% removal has been found with secondary activated sludge treatment. Acute toxicity in fish, as indicated by 96h LC50 tests, is in the range of 1,000–3,000 ug L−1 for carbon chain lengths less than C14. LC50 values for chain lengths greater than C14 range from 600 to 1400 ug L−1. Chronic toxicity data for fish is 420 ug/L. When normalized to C12.9, the NOEC is 310 ug L−1 for growth and hatchability.
- Functional group
- Amine, NR3
- Hydroxylamine, NR2OH
- Phosphine oxide, PR3=O
- Sulfoxide, R2S=O
- Azoxy, RN=N+(O−)R RN=N+RO−
- TEMPO (2,2,6,6-Tetramethylpiperidine-1-oxyl), a stable amine oxide radical
- Organisation for Economic Co-operation and Development (OECD) (2006). "Amine Oxides". OECD Existing Chemicals Database. Archived from the original on 22 February 2014.
- Sanderson, H; C Tibazarwa; W Greggs; DJ Versteeg (2009). "High Production Volume Chemical Amine Oxides [C8–C20]". Risk Analysis. 29 (6): 857–867. doi:10.1111/j.1539-6924.2009.01208.x.
- Modler, RF; Inoguchi Y (2004). "CEH Marketing Research Report: Surfactants, Household Detergents, and their Raw Materials". Chemical Economics Handbook. Menlo Park, CA: SRI Consulting.
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- Recent trends in the chemistry of pyridine N-oxides Shaker Youssif Arkivoc 2001 Link
- Waldmann, T.; et al. (2012). "Oxidation of an Organic Adlayer: A Bird's Eye View". Journal of the American Chemical Society. 134: 8817. PMID 22571820. doi:10.1021/ja302593v.
- J. Meisenheimer, Ber. 52. 1667 (1919)
- March's Advanced Organic Chemistry: Reactions, Mechanisms, and Structure Michael B. Smith, Jerry March Wiley-Interscience, 5th edition, 2001, ISBN 0-471-58589-0
- Grierson, D (1990). "The Polonovski Reaction". Org. React. 39: 85. doi:10.1002/0471264180.or039.02.
- M. Polonovski, M. Polonovski, Bull. Soc. Chim. France 41, 1190 (1927).
- Strategic Applications of Named Reactions in Organic Synthesis (Paperback) by Laszlo Kürti, Barbara Czako ISBN 0-12-429785-4.