p-Phenylenediamine

p-Phenylenediamine (PPD) is an organic compound with the formula C6H4(NH2)2. This derivative of aniline is a white solid, but samples can darken due to air oxidation.[1] It is mainly used as a component of engineering polymers and composites like kevlar. It is also an ingredient in hair dyes and is occasionally used as a substitute for henna.

p-Phenylenediamine
Names
Preferred IUPAC name
Benzene-1,4-diamine
Other names
Paraphenylenediamine
1,4-Diaminobenzene
1,4-Phenylenediamine
Identifiers
3D model (JSmol)
749029
ChEBI
ChEMBL
ChemSpider
DrugBank
ECHA InfoCard 100.003.096
EC Number
  • 203-404-7
KEGG
RTECS number
  • SS8050000
UNII
UN number 1673
Properties
C6H8N2
Molar mass 108.144 g·mol−1
Appearance White crystalline solid, darkens upon exposure to air[1]
Melting point 145 to 147 °C (293 to 297 °F; 418 to 420 K)[1]
Boiling point 267 °C (513 °F; 540 K)[1]
10% at 40°C, 87% at 107 C, 100% at 140 C [2]
Vapor pressure <1 mmHg (20°C)[3]
Acidity (pKa)
  • 2.97 (doubly protonated form; 20 °C, H2O)
  • 6.31 (conjugate acid; 20 °C, H2O)[4]
-70.28·10−6 cm3/mol
Hazards
GHS pictograms
GHS Signal word Danger
GHS hazard statements
 H301, H311, H317, H319, H331, H400, H410
P261, P264, P270, P271, P272, P273, P280, P301+310, P302+352, P304+340, P305+351+338, P311, P312, P321, P322, P330, P333+313, P337+313, P361, P363, P391, P403+233, P405, P501
Flash point 156 °C; 312 °F; 429 K [3]
400 °C
Lethal dose or concentration (LD, LC):
80 mg/kg (rat, oral)
98 mg/kg (rat, oral)
145 mg/kg (guinea pig, oral)[5]
250 mg/kg (rabbit, oral)
100 mg/kg (cat, oral)[5]
NIOSH (US health exposure limits):
PEL (Permissible)
 TWA 0.1 mg/m3 [skin][3]
REL (Recommended)
 TWA 0.1 mg/m3 [skin][3]
IDLH (Immediate danger)
 25 mg/m3[3]
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Infobox references

Production

PPD is produced via three routes. Most commonly, 4-nitrochlorobenzene is treated with ammonia and the resulting 4-nitroaniline is then hydrogenated:

ClC6H4NO2 + 2 NH3 → H2NC6H4NO2 + NH4Cl
H2NC6H4NO2 + 3 H2 → H2NC6H4NH2 + 2 H2O

In the DuPont route, aniline is converted to diphenyltriazine, which is converted by acid-catalysis to 4-aminoazobenzene. Hydrogenation of the latter affords PPD.[6]

Uses

Precursor to polymers

PPD is a precursor to aramid plastics and fibers such as Kevlar and Twaron. These applications exploit PPD's difunctionality, i.e. the presence of two amines which allow the molecules to be strung together. This polymer arises from the reaction of PPD and terephthaloyl chloride. The reaction of PPD with phosgene gives the diisocyanate, a precursor to urethane polymers.[6]

Molecular structure of Kevlar: the monomer subunit is bolded, dashed lines indicate hydrogen bonds.

Dyeing

This compound is a common hair dye. Its use is being supplanted by other aniline analogues and derivatives such as 2,5-diamino(hydroxyethylbenzene and 2,5-diaminotoluene). Other popular derivatives include tetraaminopyrimidine and indoanilines and indophenols. Derivatives of diaminopyrazole give red and violet colours.[7] In these applications, the nearly colourless dye precursor oxidizes to the dye.

Rubber antioxidant

PPD is easily oxidized, and for this reason, derivatives of PPD are used as antiozonants in the production of rubber products (e.g., IPPD). The substituents (naphthyl, isopropyl, etc.) affect the effectiveness of their antioxidant roles as well as their properties as skin irritants.[8]

Other uses

A substituted form of PPD sold under the name CD-4 is also used as a developing agent in the C-41 color photographic film development process, reacting with the silver grains in the film and creating the colored dyes that form the image.

PPD is also used as a Henna surrogate for temporary tattoos. Its usage can lead to severe contact dermatitis.

PPD is also used as a histological stain for lipids such as myelin.

PPD is used by Lichenologists in the PD test to aid identification of Lichens.[9] PPD is used extensively as a cross-linking agent in the formation of COFs (covalent organic frameworks), which have a number of applications in dyes and aromatic compounds adsorption.

Safety

The aquatic LD50 of PPD is 0.028 mg/L.[6] The U.S. Environmental Protection Agency reported that in rats and mice chronically exposed to PPD in their diet, it simply depressed body weights, and no other clinical signs of toxicity were observed in several studies.[10] One review of 31 English-language articles published between January 1992 and February 2005 that investigated the association between personal hair dye use and cancer as identified through the PubMed search engine found "at least one well-designed study with detailed exposure assessment" that observed associations between personal hair dye use and non-Hodgkin's lymphoma, multiple myeloma, acute leukemia, and bladder cancer,[11] but those associations were not consistently observed across studies. A formal meta-analysis was not possible due to the heterogeneity of the exposure assessment across the studies.

Patch test

In 2005–06, it was the tenth-most-prevalent allergen in patch tests (5.0%).[12]

The CDC lists PPD as being a contact allergen. Exposure routes are through inhalation, skin absorption, ingestion, and skin and/or eye contact; symptoms of exposure include throat irritation (pharynx and larynx), bronchial asthma, and sensitization dermatitis.[13][14] Sensitization is a lifelong issue, which may lead to active sensitization to products, including but not limited to black clothing, various inks, hair dye, dyed fur, dyed leather, and certain photographic products. It was voted Allergen of the Year in 2006 by the American Contact Dermatitis Society.

Poisoning by PPD is rare in western countries.[15]

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gollark: If they say your board is pre-updated, get one, I guess, unless you need PCIe 4.0 (hint: probably not).

See also

References
  1. Merck Index, 11th Edition, 7256
  2. "Archived copy". Archived from the original on 2012-03-13. Retrieved 2011-07-14.CS1 maint: archived copy as title (link)
  3. NIOSH Pocket Guide to Chemical Hazards. "#0495". National Institute for Occupational Safety and Health (NIOSH).
  4. Haynes, William M., ed. (2016). CRC Handbook of Chemistry and Physics (97th ed.). CRC Press. pp. 5–89. ISBN 978-1498754286.
  5. "p-Phenylene diamine". Immediately Dangerous to Life and Health Concentrations (IDLH). National Institute for Occupational Safety and Health (NIOSH).
  6. Robert A. Smiley "Phenylene- and Toluenediamines" in Ullmann's Encyclopedia of Industrial Chemistry, 2002, Wiley-VCH, Weinheim. doi:10.1002/14356007.a19_405
  7. Thomas Clausen et al. "Hair Preparations" in Ullmann's Encyclopedia of Industrial Chemistry, 2007, Wiley-VCH, Weinheim. doi:10.1002/14356007.a12_571.pub2
  8. Hans-Wilhelm Engels et al., "Rubber, 4. Chemicals and Additives" in Ullmann's Encyclopedia of Industrial Chemistry, 2007, Wiley-VCH, Weinheim. doi:10.1002/14356007.a23_365.pub2
  9. "Chemical Tests". The British Lichen Society. Retrieved 2019-04-30.
  10. p-Phenylenediamine, U.S. Environmental Protection Agency
  11. Rollison, DE; Helzlsouer, KJ; Pinney, SM (2006). "Personal hair dye use and cancer: a systematic literature review and evaluation of exposure assessment in studies published since 1992". Journal of Toxicology and Environmental Health Part B: Critical Reviews. 9 (5): 413–39. doi:10.1080/10937400600681455. PMID 17492526.
  12. Zug KA, Warshaw EM, Fowler JF Jr, Maibach HI, Belsito DL, Pratt MD, Sasseville D, Storrs FJ, Taylor JS, Mathias CG, Deleo VA, Rietschel RL, Marks J. Patch-test results of the North American Contact Dermatitis Group 2005–2006. Dermatitis. 2009 May–Jun;20(3):149-60.
  13. "The NIOSH Pocket Guide to Chemical Hazards". Archived from the original on 2017-10-24. Retrieved 2017-09-07.
  14. "NIOSH Registry of Toxic Effects of Chemical Substances (RTECS) entry for p-Phenylenediamine (PPD)". Archived from the original on 2010-03-31. Retrieved 2017-09-07.
  15. Ashraf, W.; Dawling, S.; Farrow, L. J. (1994). "Systemic Paraphenylenediamine (PPD) Poisoning: A Case Report and Review". Human & Experimental Toxicology. 13 (3): 167–70. doi:10.1177/096032719401300305. PMID 7909678.
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