Musk xylene

Musk xylene is a synthetic musk fragrance which mimics natural musk. It has been used as a perfume fixative in a wide variety of consumer products, and is still used in some cosmetics and fragrances.

Musk xylene[1]
Names
Preferred IUPAC name
1-tert-Butyl-3,5-dimethyl-2,4,6-trinitrobenzene
Identifiers
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
ECHA InfoCard 100.001.210
EC Number
  • 201-329-4
KEGG
MeSH musk+xylene
UNII
UN number 2956
Properties
C
12H
15N
3O
6
Molar mass 297.2640 g mol−1
Appearance Yellow crystals
Odor Musk-like
Melting point 110 °C (230 °F; 383 K)
150 ng dm−1
log P 4.369
Vapor pressure 9.7 mPa (at 40 °C)
Hazards
E Xn N
R-phrases (outdated) R2, R40, R50/53
S-phrases (outdated) (S2), S36/37, S46, S60, S61
Flash point 2 °C (36 °F; 275 K)
305 to 341 °C (581 to 646 °F; 578 to 614 K)
Related compounds
Related nitro musks
 Musk ambrette
Related compounds
 Trinitrotoluene
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
N verify (what is YN ?)
Infobox references

Musk xylene was once the most widely used of the "nitro-musks", but its use has declined sharply since the mid-1980s due to safety and environmental concerns. Its explosive and carcinogenic hazards are recognized to be borderline, and musk xylene is a useful example of the lowest level of such risks which need to be taken into account. However, it is a very persistent and very bioaccumulative pollutant in the aquatic environment (vPvB substance), and is the first substance to be proposed as a "substance of very high concern" (SVHC) for these reasons alone under the European Union REACH Regulation. Since no company has applied for authorisation, it is banned in the EU.[2]

Production and use

Musk xylene is produced from meta-xylene (1,3-dimethylbenzene), by a Friedel–Crafts alkylation with tert-butyl chloride and aluminium chloride followed by nitration with fuming nitric acid or with a 70:30 mixture of nitric acid and sulfuric acid. The crude product is recrystallized from 95% ethanol.[3]

Use of musk xylene in various domestic products
ProductMass fraction (%)
Skin cream0.0075
Deodorant0.0075
Shampoo0.01
Household detergents0.02
Aftershave0.03
Toilet soap0.04
Air freshener0.07
Cologne/eau de toilette0.075
Fine fragrance0.05–0.1
Sources: International Agency for Research on Cancer (1996); European Union Risk Assessment Report (2005).
NOTE: Use of musk xylene varies widely between different countries and manufacturers; these figures should be regarded as indicative maxima for the period 1990–present.

Musk xylene has been used in a wide variety of consumer products since the early 1900s, usually in very small quantities. World production of nitro musks in 1987 was about 2500 tonnes, but had fallen to about 1000 tonnes by the early 1990s: musk xylene made up roughly two-thirds of the production of nitro musks during this period. Production was concentrated in Western Europe, with the United Kingdom alone accounting for 28% of world production of nitro musks.[4][5]

Use of musk xylene continued to decline through the 1990s, as fragrance manufacturers voluntarily switched to alternative fragrance compounds.[6] For example, musk xylene has not been used in Japanese products (on a voluntary basis) since 1982,[4] and the Association of the German Toiletries and Detergents Industry (IKW) recommended the replacement of musk xylene by another compound in 1993.[7] Production of musk xylene in the European Union came to a halt and, by 2000 (the last year for which full data are available), imports to Europe were only 67 tonnes, with China as the most important source.[7] The estimated 2008 usage of musk xylene in the European Union was 25 tonnes.[8]

Musk xylene is still permitted for use in cosmetics products (except oral care products) in the European Union under the Cosmetics Directive. The permitted quantities are: up to 1% in fine fragrances; up to 0.4% in eau de toilette; up to 0.03% in other products.[9] European Union suppliers must inform their customers on request if a product contains more than 0.1% by weight of musk xylene.[10]

Safety

Musk xylene is an analogue of the explosive trinitrotoluene (TNT), so it is unsurprising that its safety characteristics have been studied in some detail. Indeed, the nitro musks were first discovered in an attempt to produce new high explosives. It has also been used – albeit in very small amounts – in mass-market consumer products for the last hundred years. The discovery of musk xylene residues in the environment prompted new concerns about its possible long-term toxicity, and led to the sharp decline in its use from the mid to late 1980s. The European Chemicals Agency has listed musk xylene as a "substance of very high concern" (SVHC) under the REACH Regulation, judging it to be "very persistent and very bioaccumulative" (vPvB) but not meeting the criteria for human or environmental toxicity to be of concern.[11]

Explosive properties

Musk xylene is used as an example case in the United Nations Manual of Test Methods and Criteria as a substance which shows some explosive properties but which does not have to be transported as Class 1 dangerous goods under the Model Regulations.[12] It is transported as small flakes in plastic bags (maximum 50 kg net mass), which are themselves within cardboard drums to avoid tearing.[13][14] This does not count as "confinement" in the meaning of explosives tests: indeed, the special packing is intended to prevent over-confinement during transport.[15]

It will explode when detonated under confinement (UN gap test[16]) or when heated under confinement (Koenen test[17]), but does not explode under the BAM fallhammer test[18] (limiting impact energy 25 J) or the BAM friction test[19] (limiting load >360 N).[12] There is no ignition, explosion, self-heating or visible decomposition when musk xylene is heated (without confinement) to 75 °C for 48 hours.[12][20]

Nevertheless, musk xylene is classified in the European Union as an explosive under the Dangerous Substances Directive[21] and as a category 1.1 explosive under the CLP Regulation.[22] The European Union classification reflects the fact that hazardous heating under confinement cannot be excluded in the industrial use of musk xylene, as opposed to its transport, and so it is necessary to warn potential users of the risk.[23]

Carcinogenicity

Musk xylene also demonstrates some of the problems of classifying substances as carcinogens. It has been placed into Group 3 ("not classifiable as to their carcinogenicity to humans") by the International Agency for Research on Cancer (IARC),[4] and is classified in the European Union as category 3 carcinogen ("cause concern for man owing to possible carcinogenic effects but in respect of which the available information is not adequate for making a satisfactory assessment") under the Dangerous Substances Directive[21] and a category 2 carcinogen ("suspected human carcinogen") under the CLP Regulation.[22]

These classifications are based mainly on a single study of oral exposure to musk xylene in B6C3F1-strain mice.[24] The mice showed a highly significant increase in liver adenomas and carcinomas at median dietary intakes of 170 mg/kg body weight (males) and 192 mg/kg body weight (females), as well as significant increases in adenomas in the Harderian gland (male mice only) and in the liver at median dietary intakes of 91 mg/kg body weight (males) and 101 mg/kg body weight (females).[24]

The European Union Risk Assessment Report makes a number of observations about this study:[25]

  • it was conducted on a single species; no studies are available on, for example, rats;
  • B6C3F1-strain mice are known to be particularly prone to liver cancers;
  • the doses were high, and toxic effects (especially on the liver) were observed in the test animals;
  • the mechanism of tumour development is unclear.

Musk xylene is not genotoxic.[26] It has significant effects on liver function which are similar to those shown by phenobarbital, for example, induction of CYP2B6 and other cytochrome P450 enzymes.[27] The human carcinogenicity of phenobarbital has been the subject of debate,[28][29] but it is currently classified in group 2B by the IARC[29] and this appears to have been an important consideration in the classification of musk xylene as a category 3 carcinogen under the Dangerous Substances Directive.[30] Nevertheless, the European Union Risk Assessment Report admits that musk xylene is a "borderline case".[25]

A further complication is the metabolism of musk xylene. One route of metabolism is through reduction of one or more nitro groups by the intestinal microflora (gut bacteria) to produce aromatic amines such as p-NH2-musk xylene.[4] This metabolite has a different liver toxicity: in particular, it inhibits the CYP1B enzymes by covalent binding.[27]

Induction of cytochrome P450 enzymes, the most likely cause of rodent carcinogenicity, is a threshold phenomenon, with a no observed effect level (NOEL) of 10 mg/kg/day in mice and a lowest observed effect level (LOEL) of 10 mg/kg/day in rats. The lowest oral dose which caused cancer (LOAEL) in B6C3F1-mice was 70 mg/kg/day.[27] These are 1–3 orders of magnitude higher than human exposure, which is principally dermal rather than oral.[31]

Environmental concerns

The first concerns about musk xylene arose in the early 1980s, with the detection of musk xylene residues in fish from the Tama River near Tokyo,[32] and subsequently in the river water itself, especially at the outlets of sewage treatment plants. This led to a voluntary moratorium on the use of musk xylene in Japan from 1982.[4] Similar residues were subsequently found in European waters such as the Elbe, Stör and Ruhr rivers in Germany, the German Bight area of the North Sea and sewage treatment plant outlets in Sweden.[4][33] Typical concentrations were >0.001 µg/l in sea water, 0.001–0.01 µg/l in river water and 0.01–0.1 µg/l (sometimes higher) in the effluent from sewage treatment plants.

These findings indicate that musk xylene is not completely removed from wastewater by the sewage treatment process. Two studies in Germany found compared musk xylene concentrations in incoming wastewater and sewage treatment plant effluent, and found removal rates of 82% and 58%.[34][35] However, they are not concentrations which are expected to be toxic to aquatic life. The European Union Risk Assessment Report reviewed more than a dozen studies of the toxicity of musk xylene to algae and to aquatic vertebrates and invertebrates, and all found no observed effect concentrations greater than 10 µg/l,[36] the chronic aquatic toxicity threshold in the EU REACH Regulation.[37]

The biodegradation of musk xylene in sea water and in mixed sea water/sediment systems was studied in laboratory simulations using carbon-14 labelled musk xylene, and the results discussed in an addendum to the European Union Risk Assessment Report.[11] The half-life in marine sediment was estimated to be 60 days or less, with biodegradation occurring by anaerobic reduction of the nitro groups. The half-life in sediment-free sea water was estimated to be more than 150 days, far above the "very persistent" threshold of 60 days.[37] The 2008 addendum also discussed the photolysis of musk xylene in water and in air, which are rapid: however, photolysis was not considered to be relevant in the persistence of musk xylene in the environment, and was not taken into account in classifying it as a "very persistent" substance.[11]

Several different primary bioaccumulation studies were reviewed in the European Union Risk Assessment Report, with bioaccumulation factors varying between 640 l/kg and 6740 l/kg.[38] Given that musk xylene has a very high octanol–water partition coefficient (log Kow = 4.9),[1] the higher bioaccumulation factors were considered to be the more significant. The 2008 addendum[11] considered a further laboratory study from the Japanese Ministry of International Trade and Industry which was not available to the authors of the original Risk Assessment Report and which also showed bioaccumulation factors in fish (Cyprinus carpio) that were higher than the REACH threshold[37] of 5000 l/kg for "very bioaccumulative" substances. Bioaccumulation factors of more than 5000 l/kg (wet weight basis) have also been found in carp (Carassius carassius) and eels (Anguilla anguilla) from a sewage treatment pond.[39]

gollark: Also, you don't need the `if h then` bit, because it'll just return early if `h` doesn't exist, see?
gollark: If you're okay with hardcoding the time/date you're waiting for, you can generate the Unix timestamp for it with another thing and just get the difference between that and `os.epoch "utc"`.
gollark: It needs to be pastebin.com/**raw**/whatever.
gollark: You can get the time/date in UTC and localtime with `os.date` or something, and Unix time, but I don't think there's a way to parse dates.
gollark: The rest of `pastebin` is mostly just argument parsing. Well, and handling other stuff like `put` and `run`.

References
  1. Section 1.3, European Union Risk Assessment Report (2005), pp. 6–7.
  2. "Archived copy". Archived from the original on 2015-06-16. Retrieved 2015-05-18.CS1 maint: archived copy as title (link)
  3. Bedoukian (1986).
  4. International Agency for Research on Cancer (1996).
  5. Ippen (1994).
  6. OSPAR Commission (2004).
  7. Section 2, European Union Risk Assessment Report (2005), pp. 9–10.
  8. RIVM–DHI–RPA (2008).
  9. ATP (2004) to the Cosmetics Directive.
  10. Article 31.3, REACH Regulation, at p. 108.
  11. European Chemicals Agency (2008).
  12. Section 10.5, Part I, UN Manual of Tests and Criteria, pp. 23–28.
  13. Section 4.1.1.2, European Union Risk Assessment Report (2005), p. 42.
  14. Packing instruction P409, Section 4.1.4, Part 4, UN Model Regulations, at p. 59.
  15. Special provision 133, Section 3.3.1, Part 3, UN Model Regulations, at p. 291.
  16. Section 11.4, Part I, UN Manual of Tests and Criteria, pp. 32–34.
  17. Section 11.5, Part I, UN Manual of Tests and Criteria, pp. 35–40.
  18. Section 13.4.2, Part I, UN Manual of Tests and Criteria, pp. 76–83.
  19. Section 13.5.1, Part I, UN Manual of Tests and Criteria, pp. 105–8.
  20. Section 13.6, Part I, UN Manual of Tests and Criteria, pp. 117–19.
  21. ATP (2004) to the Dangerous Substances Directive, at p. 121 (index no. 609-068-00-1).
  22. CLP Regulation, at p. 615 (index no. 609-068-00-1).
  23. Position document prepared for the European Chemicals Bureau (2002).
  24. Maekawa et al. (1990).
  25. Section 4.1.2.7.3, European Union Risk Assessment Report (2005), pp. 83–85.
  26. Section 4.1.2.6, European Union Risk Assessment Report (2005), pp. 74–77.
  27. Section 4.1.2.7.1, European Union Risk Assessment Report (2005), pp. 77–83.
  28. Williams & Whysner (1996).
  29. International Agency for Research on Cancer (2001).
  30. Meeting of the Commission Working Group on the Classification and Labelling of Dangerous Substances, 25 November 2002.
  31. Sections 4.1.1.5 & 4.1.3.5, European Union Risk Assessment Report, pp. 57 and 109–110.
  32. Yamagishi et al. (1981).
  33. Section 3.1.2.4, European Union Risk Assessment Report (2005), pp. 21–24.
  34. Eschke et al. (1994). Hahn (1993).
  35. Later studies have found higher rates of removal of musk xylene by sewage treatment plants, around 95%: European Chemicals Agency (2008).
  36. Section 3.2.1.1, European Union Risk Assessment Report (2005), pp. 31–34.
  37. Annex XIII, REACH Regulation, at pp. 383–85.
  38. Section 3.1.1.2, European Union Risk Assessment Report (2005), pp. 12–15.
  39. Gatermann et al. (2002).

Further reading
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