THE DOPE DOULA
THE DOPE DOULA
  • HOME
  • ARTIST SEARCH
  • RESOURCES
    • DRUG DICTIONARY
    • FOR PARENTS / CAREGIVERS
    • GENDER IDENTITY
    • NAVIGATING PSYCHEDELICS
    • SOCIAL JUSTICE - RACE
    • STIGMA
    • THE WAR ON DRUGS
    • TOOLS
    • 2C CHEMICALS | 2C-B
    • 5-MEO-DMT
    • ALCOHOL
    • BENZODIAZEPINES | XANAX
    • CAT | KAT | METHCATHINONE
    • CANNABIS | WEED | DAGGA
    • COCAINE | COKE | CHARLIE
    • DMT | CHANGA
    • GHB | GBL | LIQUID E
    • HEROIN | FENTANYL| NYAOPE
    • IBOGAINE | IBOGA | WOOD
    • KAMBO
    • KETAMIN | KET | SPECIAL K
    • LSA | DATURA | SALVIA
    • LSD | ACID | TRIPS
    • MANDRAX | BUTTONS | LUDES
    • MDMA | MANDY | PILLS
    • MUSHROOMS | SHROOMS
    • SAN PEDRO | PEYOTE
    • METH | CRYSTAL | TIK
    • OVERDOSE
  • CONTACT
  • BLOG
  • More
    • HOME
    • ARTIST SEARCH
    • RESOURCES
      • DRUG DICTIONARY
      • FOR PARENTS / CAREGIVERS
      • GENDER IDENTITY
      • NAVIGATING PSYCHEDELICS
      • SOCIAL JUSTICE - RACE
      • STIGMA
      • THE WAR ON DRUGS
      • TOOLS
      • 2C CHEMICALS | 2C-B
      • 5-MEO-DMT
      • ALCOHOL
      • BENZODIAZEPINES | XANAX
      • CAT | KAT | METHCATHINONE
      • CANNABIS | WEED | DAGGA
      • COCAINE | COKE | CHARLIE
      • DMT | CHANGA
      • GHB | GBL | LIQUID E
      • HEROIN | FENTANYL| NYAOPE
      • IBOGAINE | IBOGA | WOOD
      • KAMBO
      • KETAMIN | KET | SPECIAL K
      • LSA | DATURA | SALVIA
      • LSD | ACID | TRIPS
      • MANDRAX | BUTTONS | LUDES
      • MDMA | MANDY | PILLS
      • MUSHROOMS | SHROOMS
      • SAN PEDRO | PEYOTE
      • METH | CRYSTAL | TIK
      • OVERDOSE
    • CONTACT
    • BLOG
  • HOME
  • ARTIST SEARCH
  • RESOURCES
    • DRUG DICTIONARY
    • FOR PARENTS / CAREGIVERS
    • GENDER IDENTITY
    • NAVIGATING PSYCHEDELICS
    • SOCIAL JUSTICE - RACE
    • STIGMA
    • THE WAR ON DRUGS
    • TOOLS
    • 2C CHEMICALS | 2C-B
    • 5-MEO-DMT
    • ALCOHOL
    • BENZODIAZEPINES | XANAX
    • CAT | KAT | METHCATHINONE
    • CANNABIS | WEED | DAGGA
    • COCAINE | COKE | CHARLIE
    • DMT | CHANGA
    • GHB | GBL | LIQUID E
    • HEROIN | FENTANYL| NYAOPE
    • IBOGAINE | IBOGA | WOOD
    • KAMBO
    • KETAMIN | KET | SPECIAL K
    • LSA | DATURA | SALVIA
    • LSD | ACID | TRIPS
    • MANDRAX | BUTTONS | LUDES
    • MDMA | MANDY | PILLS
    • MUSHROOMS | SHROOMS
    • SAN PEDRO | PEYOTE
    • METH | CRYSTAL | TIK
    • OVERDOSE
  • CONTACT
  • BLOG

HEROIN | SMACK | H | THAI

Substance Information Sheet

Diacetylmorphine

Diacetylmorphine or morphine diacetate (also known as diamorphine and heroin as well as colloquially as H, dope, smack, junk, brown, boy, and others) is a semi-synthetic opioid substance of the morphinan class. It is a derivative of morphine, a natural product of the opium poppy (Papaver somniferum). Heroin is known for its highly addictive properties and it makes up a large portion of the illicit traffic in narcotics.

Heroin was first synthesized from morphine by a British chemist in 1874 and was introduced as a commercial product by the Bayer Company of Germany in 1898. Although the name heroin is a trade name, it has since been widely adopted for all intents and purposes and may describe a recreational depressant that may or may not contain pure diacetylmorphine.

Class Membership

Psychoactive class - Opioid

Chemical class - Morphinan

CRITICAL WARNING

Extreme Caution

Fatal overdose may occur when opiates are combined with other depressants such as benzodiazepines, barbiturates, gabapentinoids, thienodiazepines, alcohol or other GABAergic substances.

It is strongly discouraged to combine these substances, particularly in common to heavy doses.

DANGEROUS COMBINATIONS

INTERACTIONS

  • Alcohol - Both substances potentiate the ataxia and sedation caused by the other and can lead to unexpected loss of consciousness at high doses. Place affected patients in the recovery position to prevent vomit aspiration from excess. Memory blackouts are likely
  • Amphetamines - Stimulants increase respiration rate which allows for a higher dose of opiates than would otherwise be used. If the stimulant wears off first then the opiate may overcome the user and cause respiratory arrest.
  • Benzodiazepines - Central nervous system and/or respiratory-depressant effects may be additively or synergistically present. The two substances potentiate each other strongly and unpredictably, very rapidly leading to unconsciousness. While unconscious, vomit aspiration is a risk if not placed in the recovery position blackouts/memory loss are likely.
  • Cocaine - Stimulants increase respiration rate, which allows for a higher dose of opiates than would otherwise be used. If the stimulant wears off first then the opiate may overcome the patient and cause respiratory arrest.
  • DXM - Generally considered to be toxic. CNS depression, difficulty breathing, heart issues, and liver toxicity have been observed. Additionally if one takes DXM, their tolerance of opiates goes down slightly, thus causing additional synergistic effects.
  • GHB/GBL - The two substances potentiate each other strongly and unpredictably, very rapidly leading to unconsciousness. While unconscious, vomit aspiration is a risk if not placed in the recovery position
  • Ketamine - Both substances bring a risk of vomiting and unconsciousness. If the user falls unconscious while under the influence there is a severe risk of vomit aspiration if they are not placed in the recovery position.
  • MAOIs - Coadministration of monoamine oxidase inhibitors (MAOIs) with certain opioids has been associated with rare reports of severe adverse reactions. There appear to be two types of interaction, an excitatory and a depressive one. Symptoms of the excitatory reaction may include agitation, headache, diaphoresis, hyperpyrexia, flushing, shivering, myoclonus, rigidity, tremor, diarrhoea, hypertension, tachycardia, seizures, and coma. Death has occurred in some cases.
  • MXE - MXE can potentiate the effects of opioids but also increase the risk of respiratory depression and organ toxicity.
  • Nitrous - Both substances potentiate the ataxia and sedation caused by the other and can lead to unexpected loss of consciousness at high doses. While unconscious, vomit aspiration is a risk if not placed in the recovery position. Memory blackouts are common.
  • PCP - PCP may reduce opioid tolerance, increasing the risk of overdose.
  • Tramadol - Increased risk of seizures. Tramadol itself is known to induce seizures and it may have additive effects on seizure threshold with other opioids. Central nervous system- and/or respiratory-depressant effects may be additively or synergistically present.
  • Grapefruit - While grapefruit is not psychoactive, it may affect the metabolism of certain opioids. Tramadol, oxycodone, and fentanyl are all primarily metabolized by the enzyme CYP3A4, which is potently inhibited by grapefruit juice[22]. This may cause the drug to take longer to clear from the body. it may increase toxicity with repeated doses. Methadone may also be affected[22]. Codeine and hydrocodone are metabolized by CYP2D6. People who are on medicines that inhibit CYP2D6, or that lack the enzyme due to a genetic mutation will not respond to codeine as it can not be metabolized into its active product: morphine.

FENTANYL FACT SHEET

Download PDF

IMPORTANT SAFETY CONSIDERATIONS

Black tar heroin is dangerous to inject

It's not practical to make black tar heroin sterile, for example, by heating a solution with a lighter for a minute. Black tar heroin injection is associated with Clostridium botulinuminfection. Prion: "For prion elimination, various recommendations state 121–132 °C (250–270 °F) for 60 minutes or 134 °C (273 °F) for at least 18 minutes." A pressure cooker reach 120 °C at full pressure. However, we don't recommend black tar heroin injection even if you own a pressure cooker with a PSI meter due to lack of safety data.


This form of heroin is diacetylmorphine acetate, a product of heroin production that does not require further acetylation. It differs in texture from powder heroin in that it is black, gooey, viscous, and a texture ranging from quite similar to wet asphalt and a hard rock of material. It is commonly produced in South America and is found on the western coast of the USA. 

The actual chemical contents of black tar heroin can vary from the white powder form. Black tar might contain a variable mixture of morphine derivatives, predominantly 6-MAM (6-monoacetylmorphine) which is another result of crude acetylation that occurs in the clandestine manufacturing process.

When injected into any type of tissue, this form of heroin results in an increased risk of wound botulism. Wound botulism can be fatal and leads to amputations and death at a higher rate of black tar heroin users. Because of the consistency of the substance (tar-like), it can pose a greater risk for collapsing, damaging, or infecting veins. This damage to veins leads to a higher chance of subcutaneous and intradermal injection which is not advocated from a harm reduction point of view. 


Like many other opioids, unadulterated heroin at appropriate dosages does not cause many long-term complications other than physical and psychological dependence and constipation. Outside of the extremely powerful addiction and physical dependence, the harmful or toxic aspects of opioid usage are exclusively associated with not taking the necessary precautions in regards to its administration, overdosing and using impure heroin products that contain harmful additives. 

Heavy dosages of heroin can result in severe respiratory depression which can result in dangerous or even fatal levels of anoxia (oxygen deprivation). This occurs because the breathing reflex is suppressed by agonism of µ-opioid receptors - this effect is proportional to the dosage of the substance consumed. 

Due to the nature of the unregulated drug market, illicit heroin is of widely varying and unpredictable purity. A user may prepare what they consider to be a moderate dose while actually taking far more than intended in the event of obtaining a purer product than they are used to, or may be cut unknowingly with more potent and dangerous substances such as fentanyl.[16] Depending on drug interactions and numerous other factors, death from overdose can take anywhere from several minutes to several hours and is a direct result of  respiratory depression leading onto anoxia (oxygen deprivation) resulting from the breathing reflex being suppressed by agonism of µ-opioid receptors. Some sources quote the median lethal dose (for an average 75 kg opiate-naive individual) as being between 75 and 600mg.[17]

Heroin can also cause nausea and vomiting; a significant number of deaths attributed to opioid overdose are caused by aspiration of vomit by an unconscious victim. This is when an unconscious or semi-conscious user who is lying on their back vomits into their mouth and unknowingly suffocates. It can be prevented by ensuring that one is lying on their side with their head tilted downwards so that the airways cannot be blocked in the event of vomiting while unconscious (also known as the recovery position). 

In case of a suspected or known overdose, it is advised to administer a dose of naloxone intravenously, intramuscularly, or nasally to reverse the effects of opioid agonism


As with other opioids, the chronic use of heroin can be considered extremely addictive with a high potential for abuse and is capable of causing psychological and physical dependence among certain users. When psychological or physical addiction has developed, mental and physical withdrawal symptoms and cravings may occur if a person suddenly stops their usage.

Tolerance to many of the effects of heroin develops with prolonged and repeated use. The rate at which this occurs develops at different rates for different effects, with tolerance to the constipation-inducing effects developing particularly slowly for instance. This results in users having to administer increasingly large doses to achieve the same psychoactive effects of a previously lower dose. After heroin tolerance has developed, it takes about 3 - 7 days for the tolerance to be reduced to half and 1 - 2 weeks to be back at baseline (in the absence of further consumption). Heroin presents cross-tolerance with all other opioids, meaning that after the consumption of heroin all opioids will have a reduced effect.

The risk of fatal heroin overdoses rise sharply after a period of cessation and relapse, largely because of reduced tolerance.[19] When users dose their old doses, they no longer have the physical tolerance to handle the sedative effects of heroin and overdose occurs. To account for this lack of physical tolerance, it is safer to only dose a fraction of one's usual dosage if using after a prolonged period of sobriety. It has also been found that the environment one is in can play a role in tolerance: in one scientific study, rats with the same history of heroin administration were significantly more likely to die after receiving their dose in an environment not associated with the drug in contrast to a familiar environment.[20]

Studies have shown that the subjective cognitive euphoria and physical euphoria of heroin use, which is the reinforcing component of addiction, is proportional in its' intensity to the rate at which the blood level concentrations of the drug increases.[21] Intravenous injection is the fastest route of drug administration, causing blood concentrations to rise the fastest. It is followed by smoking, suppository (anal or vaginal insertion), insufflation (snorting), and ingestion (swallowing).


OPIOID WITHDRAWAL AT HOME

A NEXT DISTRO RESOURCE

Download PDF

Special Thanks to

psychonautwiki logo

NOTICE

The Dope Doula provides information solely for educational and harm reduction purposes. We do not promote, sell, or facilitate the sale of illegal substances on this website. It is important to note that we do not endorse or encourage the use of illegal compounds. Our aim is to provide accurate and balanced information to promote safety, health, and responsible decision-making.

While we acknowledge that substance use may occur despite legal prohibitions, we firmly advocate for personal well-being and safety. Our content is designed to raise awareness about potential risks and provide harm-reduction strategies for individuals who choose to use substances. We emphasize the importance of informed choices, consent, and responsible behaviour.


Copyright © 2024 The Dope Doula - All Rights Reserved.

  • Services
  • OVERDOSE
  • Terms of Use
  • Privacy Policy
  • Artist Search Agreements

Powered by

We're Moving!


This website will close in a few days.
All harm reduction resources are systematically being added, and all updates will be available on Substack soon!

Thank you for being part of the journey — see you there!

Take me to the Stack

Let's get this over with...

We use cookies to analyze website traffic and provide an epic experience.  Since consent is a big deal, please be explicit:

🚫ᴅᴇᴄʟiɴᴇ✅ ᴄᴏɴꜱᴇɴᴛ