Black tar heroin

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Black tar heroin

Black tar heroin, also known as black dragon, is a form of heroin that is sticky like tar or hard like coal. Its dark color is the result of crude processing methods that leave behind impurities. Despite its name, black tar heroin can also be dark orange or dark brown in appearance. [1]

Contents

Black tar heroin is impure diacetylmorphine. Other forms of heroin require additional steps of purification post acetylation. With black tar, the product's processing stops immediately after acetylation. Its unique consistency however is due to acetylation without a reflux apparatus. As in homebake heroin in Australia and New Zealand the crude acetylation results in a gelatinous mass.

Black tar as a type holds a variable admixture of morphine derivatives—predominantly 6-MAM (6-monoacetylmorphine), which is another result of crude acetylation. The lack of proper reflux during acetylation fails to remove much of the moisture retained in the acetylating agent, acetic anhydride. The acetic anhydride reacts with the moisture to produce the milder acetylating agent glacial acetic acid which is unable to acetylate the 3 position of the morphine molecule.

Black tar heroin is often produced in Latin America, [2] [3] and is most commonly found in the western and southern parts of the United States, while also being occasionally found in Western Africa. It has a varying consistency depending on manufacturing methods, cutting agents, and moisture levels, from tarry goo in the unrefined form to a uniform, light-brown powder when further processed and cut with a variety of agents. One of the more notable compounds added to heroin is lactose. [4]

Composition

Pure morphine and heroin are both fine white powders. Black tar heroin's unique appearance and texture are due to its acetylation without the benefit of the usual reflux apparatus. [5]

The assumption that tar has fewer adulterants and diluents is a misconception. [6] The most common adulterant is lactose, [7] which is added to tar via dissolving of both substances in a liquid medium, reheating and filtering, and then recrystallizing. This process is very simple and can be accomplished in any kitchen with no level of expertise needed.[ citation needed ]

The price per kilogram of black tar heroin has increased from one-tenth that of South American powder heroin in the mid-1990s to between one-half and three-quarters in 2003 due to increased distributional acumen combined with increased demand in black tar's traditional realm of distribution. Black tar heroin distribution has steadily risen in recent years, while that of U.S. East Coast powder varieties has dropped; heroin production in Colombia decreased from the late 1990s into the early 2000s. [8]

Adverse effects

People who intravenously inject black tar heroin are at higher risk of venous sclerosis than those injecting powder heroin. In this condition, the veins narrow and harden which makes repeated injection there nearly impossible. [9]

The presence of 6-monoacetylcodeine found in tar heroin has not been tested in humans but has been shown to be toxic alone and more toxic when mixed with mono- or di- acetyl morphine, potentially making tar more toxic than refined diamorphine. [10] [11]

Black tar heroin injectors can be at increased risk of life-threatening bacterial infections, in particular necrotizing soft tissue infection. [12] The practice of "skin-popping" or subcutaneous injection predisposes to necrotizing fasciitis or necrotizing cellulitis from Clostridium perfringens , while deep intramuscular injection predisposes to necrotizing myositis. [13]

Tar heroin injection can also be associated with Clostridium botulinum infection. Since the final stage of black tar heroin production would kill any spores (a combination of high temperature and strong acid), contamination is likely due to choice of cutting agent. [14] Almost all cases occur in users who inject intramuscularly or subcutaneously, rather than injecting intravenously. [15]

Black tar heroin users can also be at increased risk of bone and joint infections that stem from hematogenous seeding or local extension of the skin and soft tissue infections. Any joint can be infected, though previous studies have shown that the knee and hip are most commonly affected in heroin injectors. Associated bone infections can include septic bursitis, septic tenosynovitis, and osteomyelitis. Septic arthritis and skin and soft tissue infections often present visible and/or systematic symptoms, while osteomyelitis usually presents localized pain. [16]

Alternative routes of administration

In some parts of the United States, black tar may be the only form of heroin that is available. Many users do not inject.

See also

Related Research Articles

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Heroin, also known as diacetylmorphine and diamorphine among other names, is a morphinan opioid substance synthesized from the dried latex of the Papaver somniferum plant; it is mainly used as a recreational drug for its euphoric effects. Medical-grade diamorphine is used as a pure hydrochloride salt. Various white and brown powders sold illegally around the world as heroin are routinely diluted with cutting agents. Black tar heroin is a variable admixture of morphine derivatives—predominantly 6-MAM (6-monoacetylmorphine), which is the result of crude acetylation during clandestine production of street heroin. Heroin is used medically in several countries to relieve pain, such as during childbirth or a heart attack, as well as in opioid replacement therapy.

<span class="mw-page-title-main">Morphine</span> Pain medication of the opiate family

Morphine, formerly also called morphia, is a strong opiate that is found naturally in opium, a dark brown resin produced by drying the latex of opium poppies. It is mainly used as an analgesic. There are numerous methods used to administer morphine: oral; sublingual; via inhalation; injection into a muscle, injection under the skin, or injection into the spinal cord area; transdermal; or via rectal suppository. It acts directly on the central nervous system (CNS) to induce analgesia and alter perception and emotional response to pain. Physical and psychological dependence and tolerance may develop with repeated administration. It can be taken for both acute pain and chronic pain and is frequently used for pain from myocardial infarction, kidney stones, and during labor. Its maximum effect is reached after about 20 minutes when administered intravenously and 60 minutes when administered by mouth, while the duration of its effect is 3–7 hours. Long-acting formulations of morphine are available as MS-Contin, Kadian, and other brand names as well as generically.

<span class="mw-page-title-main">Acetyl group</span> Chemical group, –C(=O)CH₃

In organic chemistry, acetyl is a functional group with the chemical formula −COCH3 and the structure −C(=O)−CH3. It is sometimes represented by the symbol Ac. In IUPAC nomenclature, acetyl is called ethanoyl.

<span class="mw-page-title-main">Harm reduction</span> Public health policies which lessen negative aspects of problematic activities

Harm reduction, or harm minimization, refers to a range of intentional practices and public health policies designed to lessen the negative social and/or physical consequences associated with various human behaviors, both legal and illegal. Harm reduction is used to decrease negative consequences of recreational drug use and sexual activity without requiring abstinence, recognizing that those unable or unwilling to stop can still make positive change to protect themselves and others.

<span class="mw-page-title-main">Club drug</span> Category of recreational drugs

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<span class="mw-page-title-main">Necrotizing fasciitis</span> Infection that results in the death of the bodys soft tissue

Necrotizing fasciitis (NF), also known as flesh-eating disease, is a bacterial infection that results in the death of parts of the body's soft tissue. It is a severe disease of sudden onset that spreads rapidly. Symptoms usually include red or purple skin in the affected area, severe pain, fever, and vomiting. The most commonly affected areas are the limbs and perineum.

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<span class="mw-page-title-main">Clandestine chemistry</span> Illegal preparation of chemicals

Clandestine chemistry is chemistry carried out in secret, and particularly in illegal drug laboratories. Larger labs are usually run by gangs or organized crime intending to produce for distribution on the black market. Smaller labs can be run by individual chemists working clandestinely in order to synthesize smaller amounts of controlled substances or simply out of a hobbyist interest in chemistry, often because of the difficulty in ascertaining the purity of other, illegally synthesized drugs obtained on the black market. The term clandestine lab is generally used in any situation involving the production of illicit compounds, regardless of whether the facilities being used qualify as a true laboratory.

<span class="mw-page-title-main">Oxymorphone</span> Opioid analgesic drug

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<span class="mw-page-title-main">Drug injection</span> Method of introducing a drug

Drug injection is a method of introducing a drug into the bloodstream via a hollow hypodermic needle, which is pierced through the skin into the body. Intravenous therapy, a form of drug injection, is universally practiced in modernized medical care. As of 2004, there were 13.2 million people worldwide who self-administered injection drugs outside of medical supervision, of which 22% are from developed countries.

<span class="mw-page-title-main">Dipropanoylmorphine</span> Opioid analgesic drug

Dipropanoylmorphine is an opiate derivative, the 3,6-dipropanoyl ester of morphine. It was developed in 1972 as an analgesic. It is rarely used in some countries for the relief of severe pain such as that caused by terminal cancer, as an alternative to diamorphine (heroin) and morphine. The drug was first synthesised circa or about 1875 in Great Britain along with many other esters of morphine, all of which were shelved at the time, some of which were later developed such as heroin (1898), acetylpropionylmorphine (1924), dibenzoylmorphine, and so on. The name of this drug is also given as 3,6-dipropanoylmorphine and its 6-mono-acetylated homologue is also a longer-acting heroin-like drug, as are 3,6-diformylmorphine and 6-formylmorphine.

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Desomorphine is a semi-synthetic opioid commercialized by Roche, with powerful, fast-acting effects, such as sedation and analgesia. It was first discovered and patented by a German team working for Knoll in 1920 but was not generally recognized. It was later synthesized in 1932 by Lyndon Frederick Small. Small also successfully patented it in 1934 in the United States. Desomorphine was used in Switzerland under the brand name Permonid and was described as having a fast onset and a short duration of action, with relatively little nausea compared to equivalent doses of morphine. Dose for dose it is eight to ten times more potent than morphine.

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<span class="mw-page-title-main">Intravitreal injection</span> Method of administration of drugs into the eye by injection with a fine needle

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References

  1. "Types of Heroin". Indiana Prevention Resource Center. 2014.
  2. "Mexican Drug Exports", retrieved 2015/04/04
  3. "Heroin by Area of Origin", retrieved 2015/04/04
  4. "What Is Heroin Cut With? - Sunshine Behavioral Health". Sunshine Behavioral Health. 2020-07-08. Retrieved 2023-07-01.
  5. "Opium Poppy' Cultivation and Heroin Processing in Southeast Asia" (PDF). Department of Justice . 1992. pp. 32–34. Archived (PDF) from the original on 2023-12-16. Retrieved 2023-12-16.
  6. Coomber, Ross (2006). Pusher myths: re-situating the drug dealer. London: Free Association Books. ISBN   978-1-85343-948-3.
  7. Kumar, Virkeshwar; Dash, Susmita (2021-10-07). "Evaporation-Based Low-Cost Method for the Detection of Adulterant in Milk". ACS Omega. 6 (41): 27200–27207. doi:10.1021/acsomega.1c03887. ISSN   2470-1343. PMC   8529649 . PMID   34693139.
  8. <https://web.archive.org/web/20101206095810/http://www.justice.gov/ndic/pubs31/31379/heroin.htm
  9. Pieper, Barbara; Templin, Thomas N.; Kirsner, Robert S.; Birk, Thomas J. (2009). "Impact of injection drug use on distribution and severity of chronic venous disorders". Wound Repair and Regeneration. 17 (4): 485–491. doi:10.1111/j.1524-475X.2009.00513.x. ISSN   1067-1927. PMC   2748060 . PMID   19614913.
  10. Jones, Joseph T.; Jones, Mary; Jones, Brian; Sulaiman, Kristin; Plate, Charles; Lewis, Douglas (2015). "Detection of Codeine, Morphine, 6-Monoacetylmorphine, and Meconin in Human Umbilical Cord Tissue: Method Validation and Evidence of In Utero Heroin Exposure". Therapeutic Drug Monitoring. 37 (1): 45–52. doi:10.1097/FTD.0000000000000104. ISSN   0163-4356. PMC   4297219 . PMID   24901495.
  11. Murrin, L. Charles (2008-01-01), Enna, S. J.; Bylund, David B. (eds.), "Heroin", xPharm: The Comprehensive Pharmacology Reference, New York: Elsevier, pp. 1–9, ISBN   978-0-08-055232-3 , retrieved 2023-12-16
  12. Saldana, Carlos S.; Vyas, Darshali A.; Wurcel, Alysse G. (2020-08-08). "Soft Tissue, Bone, and Joint Infections in People Who Inject Drugs". Infectious Disease Clinics of North America. 34 (3): 495–509. doi:10.1016/j.idc.2020.06.007. ISSN   0891-5520. PMC   8757538 . PMID   32782098.
  13. Gonzales y Tucker, Richard Diego; Frazee, Bradley (2014-12-01). "View from the front lines: An emergency medicine perspective on clostridial infections in injection drug users". Anaerobe. 30: 108–115. doi:10.1016/j.anaerobe.2014.09.005. ISSN   1075-9964. PMID   25230330.
  14. Passaro, Douglas J. (1998-03-18). "Wound Botulism Associated with Black Tar Heroin Among Injecting Drug Users". JAMA. 279 (11): 859–863. doi: 10.1001/jama.279.11.859 . ISSN   0098-7484. PMID   9516001.
  15. "Injection Drug Use and Wound Botulism". Centers for Disease Control and Prevention. 2018-10-09. Retrieved 2021-06-19.
  16. Saldana, Carlos S.; Vyas, Darshali, A.; Wurcel, Alysse G. (1 September 2020). "Soft Tissue, Bone, and Joint Infections in People Who Inject Drugs". Infectious Disease Clinics of North America. 34 (3). Elsevier Inc.: 495–509. doi:10.1016/j.idc.2020.06.007. PMC   8757538 . PMID   32782098.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  17. Maxwell, Jane Carlisle; Spence, Richard T. (2006-01-01). "An Exploratory Study of Inhalers and Injectors Who Used Black Tar Heroin". Journal of Maintenance in the Addictions. 3 (1): 61–82. doi:10.1300/J126v03n01_06. ISSN   1091-1332. PMC   3088121 . PMID   21552428.
  18. de Virgilio, Christian (2015), de Virgilio, Christian; Frank, Paul N.; Grigorian, Areg (eds.), "Question Sets and Answers", Surgery: A Case Based Clinical Review, vol. 156, no. 3, New York, NY: Springer, pp. 591–699, doi:10.1007/978-1-4939-1726-6_59, ISBN   978-1-4939-1726-6, PMC   7120678 , PMID   25061003 , retrieved 2023-12-16
  19. Strang, J.; Griffiths, P.; Gossop, M. (June 1997). "Heroin smoking by 'chasing the dragon': origins and history". Addiction. 92 (6): 673–683, discussion 685–695. doi:10.1046/j.1360-0443.1997.9266734.x. ISSN   0965-2140. PMID   9246796.
  20. Ciccarone, Daniel (May 2009). "Heroin in brown, black and white: Structural factors and medical consequences in the US heroin market". The International Journal on Drug Policy. 20 (3): 277–282. doi:10.1016/j.drugpo.2008.08.003. ISSN   0955-3959. PMC   2704563 . PMID   18945606.
  21. Mars, Sarah G.; Ondocsin, Jeff; Ciccarone, Daniel (2018-05-16). "Toots, tastes and tester shots: user accounts of drug sampling methods for gauging heroin potency". Harm Reduction Journal. 15 (1): 26. doi: 10.1186/s12954-018-0232-z . ISSN   1477-7517. PMC   5956544 . PMID   29769132.