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Dissociative

Nitrous

Also called Nitrous Oxide, Laughing Gas, Hippy Crack, NOS, Nitro, N2O, Nangs

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Common dose · Inhaled8–16 g (1–2 cartridges) PW
Onset5–10 seconds PW
Total1–5 minutes PW
After-effects15–30 minutes PW

Dosage

Inhaled

SourceThresholdLightCommonStrongHeavy
PsychonautWiki4 g PW4–8 g (1/2–1 cartridges) PW8–16 g (1–2 cartridges) PW16–40 g (2–5 cartridges) PW40 g+ (>5 cartridges) PW
What dose are you on? (self-reported, unverified)
Read this first. These numbers come from anonymous visitors typing in a box. Nobody checks them. People misjudge, mistype, troll, or take untested products of unknown strength. They are not a dose guide and never override the sourced table above. They exist only so the sourced ranges can be compared with what people say they take. If you are deciding what to take, use the sourced table, start low, and read the risks section.
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Duration

Route · sourceOnsetCome-upPeakOffsetTotalAfter-effects
Inhaled · PsychonautWiki5–10 seconds PW5–10 seconds PW15–30 seconds PW1–5 minutes PW1–5 minutes PW15–30 minutes PW

TripSit factsheet

Onset
0-1 minutes TS
Duration
1-5 minutes TS
Aftereffects
15-30 minutes TS

Mixing

Acute combinations: what happens when these are taken close together. Entries backed by a medical journal or agency are listed first.

Backed by medical journals

Awaiting sourcePeer-reviewed reports on acute combinations, from PubMed and the journals the harm reduction sites cite.

Other documented combinations

  • Uncertain Alcohol - 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 likely. PW
  • Uncertain GHB - 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 likely. PW
  • Uncertain GBL - 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 likely. PW
  • Uncertain Opioids - 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 likely. PW
  • Uncertain Tramadol - 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 likely. PW

TripSit combination chart

TripSit rates each pairing. Only pairings with a number carry a citation from TripSit. See the whole chart, with TripSit's note for every pairing.

Caution

Low Risk & Synergy

2c-t-x TS2c-x TS5-meo-xxt TSamphetamines TSamt TScannabis TScocaine TSdextromethorphan TSdmt TSdox TSketamine TSlsd TSmdma TSmescaline TSmushrooms TSmxe TSnbomes TSpcp TS

Low Risk & No Synergy

caffeine TSlithium[19] TSmaois TSssris TS

Low Risk & Decrease

Risks and toxicity

The exact toxic dosage is unknown. Potential problems include: PW

  • Nitrous temporarily inhibits methionine synthase, a B12-dependant enzyme responsible for many important functions in the body. Heavy and frequent long-term use can deplete vitamin B12 in the body and lead to serious and unpleasant neurological problems. Users may experience numbness and tingling in the fingers, toes, lips, et al. In more severe cases, there will be numbness of all extremities. Taking B12 supplements, especially in combination with a multivitamin and complete amino acid supplements, may help alleviate this problem. If one experiences these symptoms, nitrous use should be ceased immediately, and if the symptoms persist, medical attention should be sought after.[20][21] PW
  • Nitric oxide, a toxic industrial gas, is occasionally mistaken for nitrous oxide. Users should be careful they know what they are inhaling. Inhaling Nitric Oxide can permanently damage the lungs or kill. PW

It is strongly recommended that one use harm reduction practices when using this substance. PW

Risks of whipped-cream chargers compared to medical nitrous oxide

Medical nitrous oxide has been safely used as a mild anesthetic for over 150 years. PW

  • Vapor pressure PW
  • Whipped-cream chargers: Very cold temperatures of the gas can freeze the lips and throat if taken directly from a tank or whippet. Releasing the gas into a balloon first allows the gas to warm before being administered. PW
  • Medical nitrous oxide is released slowly. PW
  • Hypoxia (abnormally low level of oxygen in the tissues), particularly the entity 'diffusion hypoxia'.[22] PW
  • Whipped-cream chargers contains no oxygen. Oxygen deprivation that can cause brain injury and suffocation can result from lack of oxygen from pure nitrous oxide continuously inhaled from strap-on mask connected to a gas canister. Never use nitrous in any manner that does not provide for adequate oxygen intake. Suffocation can occur without discomfort.[23] PW
  • Medical grade nitrous oxide contains 50% nitrous oxide, and 50% oxygen. When used as an anesthetic, nitrous is always administered in combination with oxygen. PW
  • Purity PW
  • Whipped-cream chargers contains food grade. Thus, they can contain a range of impurities, such as industrial grease left over from manufacturing, and tiny particles of steel from the pierced metal. Users can filter them through a piece of cotton, cloth, or clothing to reduce the amount of impurities inhaled. Regular cleaning of nitrous dispensing devices can also reduce the harm posed by impurities.[24][25] PW
  • Medical grade nitrous oxide: Contains medical grade nitrous oxide. PW

Risk with whipping dispensers

Direct inhalation PW

Whipping dispensers is more convenient to fill balloons with than crackers. Direct inhalation of butane can cause frostbite like effects that pose a serious risk of personal injury. PW

Dangers from plastic whip cream dispensers PW

It is advised to check that all parts of a whipping dispenser are made of metal, because dispensers made of plastic have exploded and damaged, and albeit extremely rare, even killed people: PW

  • In June 2017, Rebecca Burger, 33, a fitness blogger and model, died after a whipped-cream charger exploded and struck her in the chest. PW
  • In August 2017, another woman got wounded from a whipping dispenser.[26] PW

Risks with nitrous charger crackers

A nitrous charger cracker repeatedly used to decompress cartridges without an outer layer of silicone can cause frostbite. PW

Dependence and abuse potential

As with other dissociatives, the chronic use of nitrous oxide can be considered mildly addictive with a moderate potential for abuse. PW

Tolerance to many of the effects of nitrous oxide develops with prolonged and repeated use. This results in users having to administer increasingly large doses to achieve the same effects. After that, 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). Nitrous oxide does not produce cross-tolerance with other dissocatives, meaning that after the use of nitrous oxide other dissociatives will not have a reduced effect. PW

Testing

Awaiting sourceReagent reactions and test kit guidance from a harm reduction testing service.

Effects

gigglingmood lifteuphoriasound distortiondream like stateminor to strong hallucinationsreduction of external stimulianalgesiabuzzing sensation in nerveclumsinessnauseaheadachesnumbness in extremities TS

Overview

Nitrous oxide (also known as laughing gas, nitrous, NOS, and informally as hippy-crack). Whipped cream chargers/cartridges are called whippits (also spelled “whippits”), nangs, or bulbs.[1] PW

Nitrous oxide, also known as laughing gas, often inhaled through balloons filled with canisters of the gas.. A short-acting dissociative inhalant with strong visual, mental and auditory effects. Extremely popular especially in combination with other drugs.[2][3][4] TS

Nitrous oxide (dinitrogen oxide or dinitrogen monoxide), commonly known as laughing gas or nitrous, among others, is a chemical compound, an oxide of nitrogen with the formula N₂O. At room temperature, it is a colourless non-flammable gas, and has a slightly sweet scent and flavour. At elevated temperatures, nitrous oxide is a powerful oxidiser similar to molecular oxygen.[5] WP

Nitrous oxide has significant medical uses, especially in surgery and dentistry, for its anaesthetic and pain-reducing effects, and it is on the World Health Organization's List of Essential Medicines. Its colloquial name, "laughing gas", coined by Humphry Davy, describes the euphoric effects upon inhaling it, which make it attractive as a recreational drug inducing a brief "high". It is known for its disassociative effects. When abused chronically, it may cause neurological damage through inactivation of vitamin B₁₂. It is also used as an oxidiser in rocket propellants and motor racing fuels, and as a frothing gas for whipped cream.[6–9] WP

Nitrous oxide is also an atmospheric pollutant, with a concentration of 333 parts per billion (ppb) in 2020, increasing at 1 ppb annually. It is a major scavenger of stratospheric ozone, with an impact comparable to that of CFCs. About 40% of human-caused emissions are from agriculture, as nitrogen fertilisers are digested into nitrous oxide by soil micro-organisms. As the third most important greenhouse gas, nitrous oxide substantially contributes to global warming. Reduction of emissions is an important goal in the politics of climate change.[10–18] WP

History

Awaiting sourceHistory and culture from Wikipedia or PsychonautWiki, with their citations.

Pharmacology

Mechanism of action

The pharmacological mechanism of action of inhaled N₂O is not fully known. However, it has been shown to directly modulate a broad range of ligand-gated ion channels, which likely plays a major role. It moderately blocks NMDAR and β₂-subunit-containing nACh channels, weakly inhibits AMPA, kainate, GABAA-ρ and 5-HT₃ receptors, and slightly potentiates GABAA and glycine receptors. It also has been shown to activate two-pore-domain K+ channels. While N₂O affects several ion channels, its anaesthetic, hallucinogenic and euphoriant effects are likely caused mainly via inhibition of NMDA receptor-mediated currents. In addition to its effects on ion channels, N₂O may act similarly to nitric oxide (NO) in the central nervous system. Nitrous oxide is 30 to 40 times more soluble than nitrogen.[42–45] WP

The effects of inhaling sub-anaesthetic doses of nitrous oxide may vary unpredictably with settings and individual differences; however, Jay (2008) suggests that it reliably induces the following states and sensations:[46][47][48] WP

A minority of users also experience uncontrolled vocalisations and muscular spasms. These effects generally disappear minutes after removal of the nitrous oxide source.[48] WP

Anxiolytic effect

In behavioural tests of anxiety, a low dose of N₂O is an effective anxiolytic. This anti-anxiety effect is associated with enhanced activity of GABAA receptors, as it is partially reversed by benzodiazepine site antagonists. Mirroring this, animals that have developed tolerance to the anxiolytic effects of benzodiazepines are partially tolerant to N₂O. In humans given 30% N₂O, benzodiazepine receptor antagonists reduced the subjective reports of feeling "high", but did not alter psychomotor performance.[49][50][51] WP

Analgesic effect

The analgesic effects of N₂O are linked to the interaction between the endogenous opioid system and the descending noradrenergic system. When animals are given morphine chronically, they develop tolerance to its pain-killing effects, and this also renders the animals tolerant to the analgesic effects of N₂O. Administration of antibodies that bind and block the activity of some endogenous opioids (not β-endorphin) also block the antinociceptive effects of N₂O. Drugs that inhibit the breakdown of endogenous opioids also potentiate the antinociceptive effects of N₂O. Several experiments have shown that opioid receptor antagonists applied directly to the brain block the antinociceptive effects of N₂O, but these drugs have no effect when injected into the spinal cord.[52][53] WP

Apart from an indirect action, nitrous oxide, like morphine also interacts directly with the endogenous opioid system by binding at opioid receptor binding sites.[54][55][56] WP

Conversely, α₂-adrenoceptor antagonists block the pain-reducing effects of N₂O when given directly to the spinal cord, but not when applied directly to the brain. α2B-adrenoceptor knockout mice or animals depleted in norepinephrine are nearly completely resistant to the antinociceptive effects of N₂O. Apparently N₂O-induced release of endogenous opioids causes disinhibition of brainstem noradrenergic neurons, which release norepinephrine into the spinal cord and inhibit pain signalling. Exactly how N₂O causes the release of endogenous opioid peptides remains uncertain.[57][58][59] WP

Chemistry

Formula
N2O PC
Molar mass (g/mol)
44.013 PC
IUPAC name (computed by PubChem)
nitrous oxide PC
SMILES
[N-]=[N+]=O PC
InChIKey
GQPLMRYTRLFLPF-UHFFFAOYSA-N PC
PubChem CID
948

User reports

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Pop culture

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References

  1. Other Tarendash, A. S. Let’s Review: Chemistry, the Physical Setting. July 2001
  2. Journal / agency Ketamine potentiates cerebrocortical damage induced by the common anaesthetic agent nitrous oxide in adult rats
  3. Journal / agency Severe neurotoxicity following intrathecal methotrexate with nitrous oxide sedation in a child with acute lymphoblastic leukemia
  4. Journal / agency Neurologic degeneration associated with nitrous oxide anesthesia in patients with vitamin B12 deficiency
  5. Journal / agency Nitrous oxide. 14 September 2024
  6. Journal / agency Quax, Marcel Libertus Johannes; Van Der Steenhoven, Timothy Jason; Antonius Bronkhorst, Martinus Wilhelmus Gerardus; Emmink, Benjamin Lucas. Frostbite injury: an unknown risk when using nitrous oxide as a party drug. Acta Chirurgica Belgica. 4 March 2022. doi:10.1080/00015458.2020.1782160 · PMID 32543291
  7. Other Organization, World Health. World Health Organization model list of essential medicines: 21st list 2019. 2019
  8. Harm reduction site Turner, Sally. Nitrous-Oxide: What is it good for?. 2024-08-30
  9. Journal / agency Stockton, Lindsey; Simonsen, Cameron; Seago, Susan. Nitrous Oxide-Induced Vitamin B₁₂ Deficiency. Baylor University Medical Center Proceedings. April 2017. doi:10.1080/08998280.2017.11929571 · PMID 28405070 · PMC5349816
  10. Other Nitrous Oxide (N₂O) Mole Fraction
  11. Other Trends in Atmospheric Nitrous Oxide
  12. Journal / agency Ravishankara, A. R.; Daniel, John S.; Portmann, Robert W. Nitrous Oxide (N₂O): The Dominant Ozone-Depleting Substance Emitted in the 21st Century. Science. 2 October 2009. doi:10.1126/science.1176985 · PMID 19713491
  13. Journal / agency Tian, Hanqin; Xu, Rongting; Canadell, Josep G.; Thompson, Rona L.; Winiwarter, Wilfried; Suntharalingam, Parvadha; Davidson, Eric A.; Ciais, Philippe; Jackson, Robert B.; Janssens-Maenhout, Greet; Prather, Michael J.; Regnier, Pierre; Pan, Naiqing; Pan, Shufen; Peters, Glen P.; Shi, Hao; Tubiello, Francesco N.; Zaehle, Sönke; Zhou, Feng; Arneth, Almut; Battaglia, Gianna; Berthet, Sarah; Bopp, Laurent; Bouwman, Alexander F.; Buitenhuis, Erik T.; Chang, Jinfeng; Chipperfield, Martyn P.; Dangal, Shree R. S.; Dlugokencky, Edward; Elkins, James W.; Eyre, Bradley D.; Fu, Bojie; Hall, Bradley; Ito, Akihiko; Joos, Fortunat; Krummel, Paul B.; Landolfi, Angela; Laruelle, Goulven G.; Lauerwald, Ronny; Li, Wei; Lienert, Sebastian; Maavara, Taylor; MacLeod, Michael; Millet, Dylan B.; Olin, Stefan; Patra, Prabir K.; Prinn, Ronald G.; Raymond, Peter A.; Ruiz, Daniel J.; van der Werf, Guido R.; Vuichard, Nicolas; Wang, Junjie; Weiss, Ray F.; Wells, Kelley C.; Wilson, Chris; Yang, Jia; Yao, Yuanzhi. A comprehensive quantification of global nitrous oxide sources and sinks. Nature. 8 October 2020. doi:10.1038/s41586-020-2780-0 · PMID 33028999
  14. Journal / agency Thompson, R. L. Acceleration of global N₂O emissions seen from two decades of atmospheric inversion. Nat. Clim. Change. 2019. doi:10.1038/s41558-019-0613-7
  15. Other Reduce nitrous oxide emissions. 2021-12-13
  16. Other AR5 Climate Change 2013: The Physical Science Basis
  17. Other Nitrous oxide emissions pose an increasing climate threat, study finds
  18. Other Mundschenk, Susanne. The Netherlands is showing how not to tackle climate change | The Spectator. 3 August 2022
  19. Other Drugbank. Lithium Carbonate
  20. Journal / agency Weimann, J. Toxicity of nitrous oxide. Best Practice & Research Clinical Anaesthesiology. March 2003. doi:10.1053/bean.2002.0264
  21. Forum (anecdotal) Ok-Ad5515. Warning about Nitrous Oxide. 2021
  22. Journal / agency https://pubmed.ncbi.nlm.nih.gov/3537624/
  23. Harm reduction site http://www.erowid.org/chemicals/nitrous/nitrous_health.shtml
  24. Other https://www.dancewizensw.org.au/filtering-nangs
  25. Harm reduction site http://www.erowid.org/chemicals/nitrous/nitrous_article2.shtml
  26. Journal / agency https://www.independent.co.uk/news/world/woman-whipped-cream-canister-explosion-emilie-lada-skull-crack-award-ps990000-french-court-model-death-a7880461.html
  27. Other BtMG
  28. Other NpSG
  29. Other § 2 AMG - Einzelnorm
  30. Other Anlage 1 AMVV
  31. Other Rankin, Jennifer. Dutch to ban laughing gas over fears for health and road safety. 2022-11-15
  32. Other Opium act (drugs)
  33. Other Nyheter, S. V. T. Ny lag: 18-årsgräns för köp av lustgas. 4 June 2025
  34. Other https://www.legislation.gov.uk/uksi/2023/1091/made
  35. Other US Nitrous Oxide Laws (alphabetically) Based on a search of online free legal databases. Conducted May 2002
  36. Other California Code, Penal Code - PEN § 381b
  37. Other Ohio Medical
  38. Other Anderton, Jim. Time's up for sham sales of laughing gas. 26 June 2005
  39. Other Lambeth Council bans laughing gas as recreational drug. 17 August 2015
  40. Other Nitrous oxide: Laughing gas to be illegal by end of year. 2023-09-05
  41. Other California Penal Code § 381b. 1984
  42. Journal / agency Yamakura T, Harris RA. Effects of gaseous anaesthetics nitrous oxide and xenon on ligand-gated ion channels. Comparison with isoflurane and ethanol. Anesthesiology. 2000. doi:10.1097/00000542-200010000-00034 · PMID 11020766
  43. Journal / agency Mennerick S, Jevtovic-Todorovic V, Todorovic SM, Shen W, Olney JW, Zorumski CF. Effect of nitrous oxide on excitatory and inhibitory synaptic transmission in hippocampal cultures. Journal of Neuroscience. 1998. doi:10.1523/JNEUROSCI.18-23-09716.1998 · PMID 9822732 · PMC6793274
  44. Journal / agency Gruss M, Bushell TJ, Bright DP, Lieb WR, Mathie A, Franks NP. Two-pore-domain K⁺ channels are a novel target for the anesthetic gases xenon, nitrous oxide, and cyclopropane. Molecular Pharmacology. 2004. doi:10.1124/mol.65.2.443 · PMID 14742687
  45. Journal / agency Emmanouil DE, Quock RM. Advances in Understanding the Actions of Nitrous Oxide. Anesthesia Progress. 2007. doi:10.2344/0003-3006(2007)54[9:AIUTAO]2.0.CO;2 · PMID 17352529 · PMC1821130
  46. Journal / agency Atkinson, Roland M.; Green, J. DeWayne; Chenoweth, Dennis E.; Atkinson, Judith Holmes. Subjective Effects of Nitrous Oxide: Cognitive, Emotional, Perceptual and Transcendental Experiences. Journal of Psychedelic Drugs. 1979-10-01. doi:10.1080/02791072.1979.10471415 · PMID 522172
  47. Journal / agency Walker, Diana J; Zacny, James P. Within- and between-subject variability in the reinforcing and subjective effects of nitrous oxide in healthy volunteers. Drug and Alcohol Dependence. September 2001. doi:10.1016/s0376-8716(00)00234-9 · PMID 11470344
  48. Journal / agency Jay M. Nitrous oxide: recreational use, regulation and harm reduction. Drugs and Alcohol Today. 2008-09-01. doi:10.1108/17459265200800022
  49. Journal / agency Emmanouil DE, Johnson CH, Quock RM. Nitrous oxide anxiolytic effect in mice in the elevated plus maze: mediation by benzodiazepine receptors. Psychopharmacology. 1994. doi:10.1007/BF02244768 · PMID 7862891
  50. Journal / agency Zacny JP, Yajnik S, Coalson D, Lichtor JL, Apfelbaum JL, Rupani G, Young C, Thapar P, Klafta J. Flumazenil may attenuate some subjective effects of nitrous oxide in humans: a preliminary report. Pharmacology Biochemistry and Behavior. 1995. doi:10.1016/0091-3057(95)00039-Y · PMID 7675863
  51. Journal / agency Gillman, Mark Akfred. What is better for psychiatry: Titrated or fixed concentrations of nitrous oxide?. Front. Psychiatry. 2022. doi:10.3389/fpsyt.2022.773190 · PMID 36072452 · PMC9441863
  52. Journal / agency Berkowitz BA, Finck AD, Hynes MD, Ngai SH. Tolerance to nitrous oxide analgesia in rats and mice. Anesthesiology. 1979. doi:10.1097/00000542-197910000-00006 · PMID 484891
  53. Journal / agency Branda EM, Ramza JT, Cahill FJ, Tseng LF, Quock RM. Role of brain dynorphin in nitrous oxide antinociception in mice. Pharmacology Biochemistry and Behavior. 2000. doi:10.1016/S0091-3057(99)00202-6 · PMID 10672972
  54. Journal / agency Gillman, M.A. Analgesic (sub anesthetic) nitrous oxide interacts with the endogenous opiod system: A review of the evidence. Life Sciences. October 1986. doi:10.1016/0024-3205(86)90181-5 · PMID 3020325
  55. Journal / agency Daras, Christos; Cantrill, Richard C.; Gillman, Mark A. 3HNaloxone displacement: Evidence for nitrous oxide as opioid receptor agonist. European Journal of Pharmacology. April 1983. doi:10.1016/0014-2999(83)90626-x · PMID 6305684
  56. Journal / agency Ori, Carlo; Ford-Rice, Felicia; London, Edythe D. Effects of Nitrous Oxide and Halothane on μ and κ Opioid Receptors in Guinea-pig Brain. Anesthesiology. March 1989. doi:10.1097/00000542-198903000-00027 · PMID 2564264
  57. Journal / agency Guo TZ, Davies MF, Kingery WS, Patterson AJ, Limbird LE, Maze M. Nitrous oxide produces antinociceptive response via alpha2B and/or alpha2C adrenoceptor subtypes in mice. Anesthesiology. 1999. doi:10.1097/00000542-199902000-00022 · PMID 9952154
  58. Journal / agency Sawamura S, Kingery WS, Davies MF, Agashe GS, Clark JD, Koblika BK, Hashimoto T, Maze M. Antinociceptive action of nitrous oxide is mediated by stimulation of noradrenergic neurons in the brainstem and activation of [alpha]{2B adrenoceptors. J. Neurosci. 2000. doi:10.1523/JNEUROSCI.20-24-09242.2000 · PMID 11125002 · PMC6773006
  59. Journal / agency Maze M, Fujinaga M. Recent advances in understanding the actions and toxicity of nitrous oxide. Anaesthesia. 2000. doi:10.1046/j.1365-2044.2000.01463.x · PMID 10781114

Text and values on this page are quoted from PsychonautWiki (CC BY-SA 4.0), Wikipedia (CC BY-SA 4.0), TripSit factsheets, PubChem (public domain). Each value links to the exact revision it came from.