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HXE: Difference between revisions

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>Dextromethorphan
up to visual effects
>Lustrous
m fixed link
 
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{{headerpanel|{{Approval}}}}
{{headerpanel|{{Approval}}}}
{{SummarySheet}}
{{SummarySheet}}
{{SubstanceBox
{{SubstanceBox/HXE}}
 
    <!-- Special Parameters -->
    |displayClasses={{{displayClasses|}}}
    |MaterialTable_MaxWidth=250px
    |MaterialTable_Title={{PAGENAME}}
 
    <!-- Modules -->
    |ModuleSource=false
    |ModuleCombination=false
    |ModuleStructure=true
    |ModuleNomenclature=true
    |ModuleClassMembership=true
    |ModuleROA=true
 
    <!-- Source -->
    |PhotoImageFile=
    |PhotoImageWidth=
    |PhotoImageCaption=
 
    <!-- Combination -->
    |CombinationImage1_Caption=
    |CombinationImage1_File=
    |CombinationImage1_Width=
 
    |CombinationImage2_Caption=
    |CombinationImage2_File=
    |CombinationImage2_Width=
 
    |CombinationImage3_Caption=
    |CombinationImage3_File=
    |CombinationImage3_Width=
 
    <!-- Structure -->
    |MolecularStructureCaption=
    |SkeletalImageFile=File:HXE.svg
    |SkeletalImageWidth=245px
    |3DImageFile=
    |3DImageWidth=
 
    <!-- Nomenclature -->
    |NameCommon=HXE  
    |NameSubstitution=3-HO-2'-Oxo-PCE
    |NameSystematic=2-(Ethylamino)-2-(3-hydroxyphenyl)cyclohexan-1-one
 
    <!-- Class Membership -->
    |EffectClass=[[psychoactive class::Dissociative]]
    |ChemicalClass=[[chemical class::Arylcyclohexylamine]]
 
    <!-- Dosage/Duration per ROA -->
 
    |OralROA=true
    |OralROA_Collapsed=false
    |OralROA_Caption=
    |OralROA_Bioavailability=[[Oral min bioavailability::x]]% - [[Oral max bioavailability::y]]%<ref>APA formatted citation.</ref> <!-- Refer to this tool to generate APA citations from DOI links: https://reftag.appspot.com/doiweb.py -->
    |OralROA_Microdose=
    |OralROA_Threshold=[[Oral threshold dose::30]] -  [[Oral dose units::mg]]
    |OralROA_Light=[[Oral min light dose::30]] - [[Oral max light dose::60]] mg
    |OralROA_Common=[[Oral min common dose::60]] - [[Oral max common dose::100]] mg
    |OralROA_Strong=[[Oral min strong dose::100]] - [[Oral max strong dose::130]] mg
    |OralROA_Heavy=[[Oral heavy dose::130]] mg +
    |OralROA_TimelineFile=
    |OralROA_TimelineWidth=
    |OralROA_Duration=[[Oral min total time::x]] - [[Oral max total time::y]] [[Oral total time units::hours]]
    |OralROA_Onset=[[Oral min onset time::x]] - [[Oral max onset time::y]] [[Oral onset time units::minutes]]
    |OralROA_Comeup=[[Oral min comeup time::x]] - [[Oral max comeup time::y]] [[Oral comeup time units::minutes]]
    |OralROA_Peak=[[Oral min peak time::x]] - [[Oral max peak time::y]] [[Oral peak time units::hours]]
    |OralROA_Offset=[[Oral min offset time::x]] - [[Oral max offset time::y]] [[Oral offset time units::hours]]
    |OralROA_Aftereffects=[[Oral min afterglow time::x]] - [[Oral max afterglow time::y]] [[Oral afterglow time units::hours]]
 
    |SublingualROA=true
    |SublingualROA_Collapsed=false
    |SublingualROA_Caption=
    |SublingualROA_Bioavailability=[[Sublingual min bioavailability::x]]% - [[Sublingual max bioavailability::y]]%
    |SublingualROA_Microdose=
    |SublingualROA_Threshold=[[Sublingual threshold dose::30]] - [[Sublingual dose units::mg]]
    |SublingualROA_Light=[[Sublingual min light dose::30]] - [[Sublingual max light dose::y]] mg
    |SublingualROA_Common=[[Sublingual min common dose::60]] - [[Sublingual max common dose::y]] mg
    |SublingualROA_Strong=[[Sublingual min strong dose::10ü]] - [[Sublingual max strong dose::y]] mg
    |SublingualROA_Heavy=[[Sublingual heavy dose::13ü]] mg +
    |SublingualROA_TimelineFile=
    |SublingualROA_TimelineWidth=
    |SublingualROA_Duration=[[Sublingual min total time::a]] - [[Sublingual max total time::b]] [[Sublingual total time units::hours]]
    |SublingualROA_Onset=[[Sublingual min onset time::a]] - [[Sublingual max onset time::b]] [[Sublingual onset time units::minutes]]
    |SublingualROA_Comeup=[[Sublingual min comeup time::a]] - [[Sublingual max comeup time::b]] [[Sublingual comeup time units::minutes]]
    |SublingualROA_Peak=[[Sublingual min peak time::a]] - [[Sublingual max peak time::b]] [[Sublingual peak time units::hours]]
    |SublingualROA_Offset=[[Sublingual min offset time::a]] - [[Sublingual max offset time::b]] [[Sublingual offset time units::hours]]
    |SublingualROA_Aftereffects=[[Sublingual min afterglow time::a]] - [[Sublingual max afterglow time::b]] [[Sublingual afterglow time units::hours]]
 
    |BuccalROA=false
    |BuccalROA_Collapsed=True
    |BuccalROA_Caption=
    |BuccalROA_Bioavailability=[[Buccal min bioavailability::x]]% - [[Buccal max bioavailability::y]]%<ref>APA formatted citation</ref>
    |BuccalROA_Microdose=
    |BuccalROA_Threshold=[[Buccal threshold dose::x]] -  [[Buccal dose units::mg]]
    |BuccalROA_Light=[[Buccal min light dose::x]] - [[Buccal max light dose::y]] mg
    |BuccalROA_Common=[[Buccal min common dose::x]] - [[Buccal max common dose::y]] mg
    |BuccalROA_Strong=[[Buccal min strong dose::x]] - [[Buccal max strong dose::y]] mg
    |BuccalROA_Heavy=[[Buccal heavy dose::x]] mg +
    |BuccalROA_TimelineFile=
    |BuccalROA_TimelineWidth=
    |BuccalROA_Duration=[[Buccal min total time::x]] - [[Buccal max total time::y]] [[Buccal total time units::hours]]
    |BuccalROA_Onset=[[Buccal min onset time::x]] - [[Buccal max onset time::y]] [[Buccal onset time units::minutes]]
    |BuccalROA_Comeup=[[Buccal min comeup time::x]] - [[Buccal max comeup time::y]] [[Buccal comeup time units::minutes]]
    |BuccalROA_Peak=[[Buccal min peak time::x]] - [[Buccal max peak time::y]] [[Buccal peak time units::hours]]
    |BuccalROA_Offset=[[Buccal min offset time::x]] - [[Buccal max offset time::y]] [[Buccal offset time units::hours]]
    |BuccalROA_Aftereffects=[[Buccal min afterglow time::x]] - [[Buccal max afterglow time::y]] [[Buccal afterglow time units::hours]]
 
    |InsufflatedROA=true
    |InsufflatedROA_Collapsed=false
    |InsufflatedROA_Caption=
    |InsufflatedROA_Bioavailability=[[Insufflated min bioavailability::x]]% - [[Insufflated max bioavailability::y]]%<ref>APA formatted citation</ref>
    |InsufflatedROA_Microdose=
    |InsufflatedROA_Threshold=[[Insufflated threshold dose::20]] -  [[Insufflated dose units::mg]]
    |InsufflatedROA_Light=[[Insufflated min light dose::40]] - [[Insufflated max light dose::20]] mg
    |InsufflatedROA_Common=[[Insufflated min common dose::40]] - [[Insufflated max common dose::70]] mg
    |InsufflatedROA_Strong=[[Insufflated min strong dose::70]] - [[Insufflated max strong dose::120]] mg
    |InsufflatedROA_Heavy=[[Insufflated heavy dose::120]] mg +
    |InsufflatedROA_TimelineFile=
    |InsufflatedROA_TimelineWidth=
    |InsufflatedROA_Duration=[[Insufflated min total time::4]] - [[Insufflated max total time::8]] [[Insufflated total time units::hours]]
    |InsufflatedROA_Onset=[[Insufflated min onset time::10]] - [[Insufflated max onset time::30]] [[Insufflated onset time units::minutes]]
    |InsufflatedROA_Comeup=[[Insufflated min comeup time::20]] - [[Insufflated max comeup time::40]] [[Insufflated comeup time units::minutes]]
    |InsufflatedROA_Peak=[[Insufflated min peak time::1.5]] - [[Insufflated max peak time::4]] [[Insufflated peak time units::hours]]
    |InsufflatedROA_Offset=[[Insufflated min offset time::2]] - [[Insufflated max offset time:4]] [[Insufflated offset time units::hours]]
    |InsufflatedROA_Aftereffects=[[Insufflated min afterglow time::2]] - [[Insufflated max afterglow time:7]] [[Insufflated afterglow time units::hours]]
 
    |RectalROA=false
    |RectalROA_Collapsed=True
    |RectalROA_Caption=
    |RectalROA_Bioavailability=[[Rectal min bioavailability::x]]% - [[Rectal max bioavailability::y]]
    |RectalROA_Microdose=
    |RectalROA_Threshold=[[Rectal threshold dose::x]] -  [[Rectal dose units::mg]]
    |RectalROA_Light=[[Rectal min light dose::x]] - [[Rectal max light dose::y]] mg
    |RectalROA_Common=[[Rectal min common dose::x]] - [[Rectal max common dose::y]] mg
    |RectalROA_Strong=[[Rectal min strong dose::x]] - [[Rectal max strong dose::y]] mg
    |RectalROA_Heavy=[[Rectal heavy dose::x]] mg +
    |RectalROA_TimelineFile=
    |RectalROA_TimelineWidth=
    |RectalROA_Duration=[[Rectal min total time::x]] - [[Rectal max total time::y]] [[Rectal total time units::hours]]
    |RectalROA_Onset=[[Rectal min onset time::x]] - [[Rectal max onset time::y]] [[Rectal onset time units::minutes]]
    |RectalROA_Comeup=[[Rectal min comeup time::x]] - [[Rectal max comeup time::y]] [[Rectal comeup time units::minutes]]
    |RectalROA_Peak=[[Rectal min peak time::x]] - [[Rectal max peak time::y]] [[Rectal peak time units::hours]]
    |RectalROA_Offset=[[Rectal min offset time::x]] - [[Rectal max offset time::y]] [[Rectal offset time units::hours]]
    |RectalROA_Aftereffects=[[Rectal min afterglow time::x]] - [[Rectal max afterglow time::y]] [[Rectal afterglow time units::hours]]
 
    |TransdermalROA=false
    |TransdermalROA_Collapsed=True
    |TransdermalROA_Caption=
    |TransdermalROA_Bioavailability=[[Transdermal min bioavailability::x]]% - [[Transdermal max bioavailability::y]]%<ref>APA formatted citation</ref>
    |TransdermalROA_Microdose=
    |TransdermalROA_Threshold=[[Transdermal threshold dose::x]] -  [[Transdermal dose units::mg]]
    |TransdermalROA_Light=[[Transdermal min light dose::x]] - [[Transdermal max light dose::y]] mg
    |TransdermalROA_Common=[[Transdermal min common dose::x]] - [[Transdermal max common dose::y]] mg
    |TransdermalROA_Strong=[[Transdermal min strong dose::x]] - [[Transdermal max strong dose::y]] mg
    |TransdermalROA_Heavy=[[Transdermal heavy dose::x]] mg +
    |TransdermalROA_TimelineFile=
    |TransdermalROA_TimelineWidth=
    |TransdermalROA_Duration=[[Transdermal min total time::x]] - [[Transdermal max total time::y]] [[Transdermal total time units::hours]]
    |TransdermalROA_Onset=[[Transdermal min onset time::x]] - [[Transdermal max onset time::y]] [[Transdermal onset time units::minutes]]
    |TransdermalROA_Comeup=[[Transdermal min comeup time::x]] - [[Transdermal max comeup time::y]] [[Transdermal comeup time units::minutes]]
    |TransdermalROA_Peak=[[Transdermal min peak time::x]] - [[Transdermal max peak time::y]] [[Transdermal peak time units::hours]]
    |TransdermalROA_Offset=[[Transdermal min offset time::x]] - [[Transdermal max offset time::y]] [[Transdermal offset time units::hours]]
    |TransdermalROA_Aftereffects=[[Transdermal min afterglow time::x]] - [[Transdermal max afterglow time::y]] [[Transdermal afterglow time units::hours]]
 
    |SubcutaneousROA=false
    |SubcutaneousROA_Collapsed=True
    |SubcutaneousROA_Caption=
    |SubcutaneousROA_Bioavailability=[[Subcutaneous min bioavailability::x]]% - [[Subcutaneous max bioavailability::y]]%<ref>APA formatted citation</ref>
    |SubcutaneousROA_Microdose=
    |SubcutaneousROA_Threshold=[[Subcutaneous threshold dose::x]] -  [[Subcutaneous dose units::mg]]
    |SubcutaneousROA_Light=[[Subcutaneous min light dose::x]] - [[Subcutaneous max light dose::y]] mg
    |SubcutaneousROA_Common=[[Subcutaneous min common dose::x]] - [[Subcutaneous max common dose::y]] mg
    |SubcutaneousROA_Strong=[[Subcutaneous min strong dose::x]] - [[Subcutaneous max strong dose::y]] mg
    |SubcutaneousROA_Heavy=[[Subcutaneous heavy dose::x]] mg +
    |SubcutaneousROA_TimelineFile=
    |SubcutaneousROA_TimelineWidth=
    |SubcutaneousROA_Duration=[[Subcutaneous min total time::x]] - [[Subcutaneous max total time::y]] [[Subcutaneous total time units::hours]]
    |SubcutaneousROA_Onset=[[Subcutaneous min onset time::x]] - [[Subcutaneous max onset time::y]] [[Subcutaneous onset time units::minutes]]
    |SubcutaneousROA_Comeup=[[Subcutaneous min comeup time::x]] - [[Subcutaneous max comeup time::y]] [[Subcutaneous comeup time units::minutes]]
    |SubcutaneousROA_Peak=[[Subcutaneous min peak time::x]] - [[Subcutaneous max peak time::y]] [[Subcutaneous peak time units::hours]]
    |SubcutaneousROA_Offset=[[Subcutaneous min offset time::x]] - [[Subcutaneous max offset time::y]] [[Subcutaneous offset time units::hours]]
    |SubcutaneousROA_Aftereffects=[[Subcutaneous min afterglow time::x]] - [[Subcutaneous max afterglow time::y]] [[Subcutaneous afterglow time units::hours]]
 
    |IntramuscularROA=false
    |IntramuscularROA_Collapsed=true
    |IntramuscularROA_Caption=
    |IntramuscularROA_Bioavailability=[[Intramuscular min bioavailability::x]]% - [[Intramuscular max bioavailability::y]]%<ref>APA formatted citation</ref>
    |IntramuscularROA_Microdose=
    |IntramuscularROA_Threshold=[[Intramuscular threshold dose::x]] -  [[Intramuscular dose units::mg]]
    |IntramuscularROA_Light=[[Intramuscular min light dose::x]] - [[Intramuscular max light dose::y]] mg
    |IntramuscularROA_Common=[[Intramuscular min common dose::x]] - [[Intramuscular max common dose::y]] mg
    |IntramuscularROA_Strong=[[Intramuscular min strong dose::x]] - [[Intramuscular max strong dose::y]] mg
    |IntramuscularROA_Heavy=[[Intramuscular heavy dose::x]] mg +
    |IntramuscularROA_TimelineFile=
    |IntramuscularROA_TimelineWidth=
    |IntramuscularROA_Duration=[[Intramuscular min total time::x]] - [[Intramuscular max total time::y]] [[Intramuscular total time units::hours]]
    |IntramuscularROA_Onset=[[Intramuscular min onset time::x]] - [[Intramuscular max onset time::y]] [[Intramuscular onset time units::minutes]]
    |IntramuscularROA_Comeup=[[Intramuscular min comeup time::x]] - [[Intramuscular max comeup time::y]] [[Intramuscular comeup time units::minutes]]
    |IntramuscularROA_Peak=[[Intramuscular min peak time::x]] - [[Intramuscular max peak time::y]] [[Intramuscular peak time units::hours]]
    |IntramuscularROA_Offset=[[Intramuscular min offset time::x]] - [[Intramuscular max offset time::y]] [[Intramuscular offset time units::hours]]
    |IntramuscularROA_Aftereffects=[[Intramuscular min afterglow time::x]] - [[Intramuscular max afterglow time::y]] [[Intramuscular afterglow time units::hours]]
 
    |IntravenousROA=false
    |IntravenousROA_Collapsed=true
    |IntravenousROA_Caption=
    |IntravenousROA_Bioavailability=[[Intravenous min bioavailability::x]]% - [[Intravenous max bioavailability::y]]%<ref>APA formatted citation</ref>
    |IntravenousROA_Microdose=
    |IntravenousROA_Threshold=[[Intravenous threshold dose::x]] -  [[Intravenous dose units::mg]]
    |IntravenousROA_Light=[[Intravenous min light dose::x]] - [[Intravenous max light dose::y]] mg
    |IntravenousROA_Common=[[Intravenous min common dose::x]] - [[Intravenous max common dose::y]] mg
    |IntravenousROA_Strong=[[Intravenous min strong dose::x]] - [[Intravenous max strong dose::y]] mg
    |IntravenousROA_Heavy=[[Intravenous heavy dose::x]] mg +
    |IntravenousROA_TimelineFile=
    |IntravenousROA_TimelineWidth=
    |IntravenousROA_Duration=[[Intravenous min total time::x]] - [[Intravenous max total time::y]] [[Intravenous total time units::hours]]
    |IntravenousROA_Onset=[[Intravenous min onset time::x]] - [[Intravenous max onset time::y]] [[Intravenous onset time units::minutes]]
    |IntravenousROA_Comeup=[[Intravenous min comeup time::x]] - [[Intravenous max comeup time::y]] [[Intravenous comeup time units::minutes]]
    |IntravenousROA_Peak=[[Intravenous min peak time::x]] - [[Intravenous max peak time::y]] [[Intravenous peak time units::hours]]
    |IntravenousROA_Offset=[[Intravenous min offset time::x]] - [[Intravenous max offset time::y]] [[Intravenous offset time units::hours]]
    |IntravenousROA_Aftereffects=[[Intravenous min afterglow time::x]] - [[Intravenous max afterglow time::y]] [[Intravenous afterglow time units::hours]]
 
}}
 




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{{Preamble/SubjectiveEffects}}
{{Preamble/SubjectiveEffects}}


HXE's effects resemble rather the effects of [[MXPr]], [[MXE]], [[DCK]] than more chaotic derivatives like [[O-PCE]] or [[MXiPr]]. Compared to [[MXE]], it has less of a warmth to it and is weaker in its euphoria and clearheadedness.
HXE's effects resemble rather the effects of [[MXPr]], [[MXE]], [[DCK]] than more chaotic derivatives like [[O-PCE]] or [[MXiPr]]. Compared to [[MXE]], it has less of a warmth to it and is weaker in its euphoria and clearheadedness, which can roughly be considered equal to [[MXPr]]'s potency.


{{effects/base
{{effects/base
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}}
}}
{{effects/disconnective|
*'''[[Effect::Tactile disconnection]]'''
*'''[[Effect::Visual disconnection]]''' - This eventually results in HXE's equivalent of the "k-hole" or more specifically, ''[[Visual disconnection#Holes, spaces and voids|holes, spaces and voids]]'' alongside of ''[[Visual disconnection#Structures|structures]]''.
*'''[[Effect::Consciousness disconnection]]'''
}}


}}
{{effects/visual|
{{effects/visual|
====Suppression====
====Suppression====
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*'''[[Effect::External hallucination]]''' (''[[effect::autonomous entities]]''; ''[[effect::settings, sceneries, and landscapes]]''; ''[[effect::perspective hallucinations]]'' and ''[[effect::scenarios and plots]]'') - In comparison to other [[dissociative]]s, this effect can occur at heavy doses, but is extremely infrequent in comparison to the same effect found within [[deliriant]]s. It can be comprehensively described through its [[Visual_effects:_Internal_hallucinations#Variations|variations]] as delirious in believability, autonomous in controllability and solid in style. The most common theme for this effect to follow is one of experiencing and talking to friends when they are not actually present.
*'''[[Effect::External hallucination]]''' (''[[effect::autonomous entities]]''; ''[[effect::settings, sceneries, and landscapes]]''; ''[[effect::perspective hallucinations]]'' and ''[[effect::scenarios and plots]]'') - In comparison to other [[dissociative]]s, this effect can occur at heavy doses, but is extremely infrequent in comparison to the same effect found within [[deliriant]]s. It can be comprehensively described through its [[Visual_effects:_Internal_hallucinations#Variations|variations]] as delirious in believability, autonomous in controllability and solid in style. The most common theme for this effect to follow is one of experiencing and talking to friends when they are not actually present.


}}
}}|
 
|{{effects/cognitive|
If applicable, a brief paragraph summary of the substance's cognitive effects may be included here.


You may select from a list of cognitive effects to add below [[Subjective effect index#Cognitive effects|here]].
{{effects/cognitive|
HXE is generally considered to be euphoric and comfortable. It can also turn mildly confusing, although it's manageable and not nearly as wild as [[O-PCE]] or [[MXiPr]]. It is mostly clear-headed in comparison to that of [[DXM]] and [[ketamine]]. The specific cognitive effects can be broken down into several separate subcomponents which are listed and described below:


*'''[[Effect::Cognitive effect1]]'''  
*'''[[Effect::Amnesia]]'''
*'''[[Effect::Cognitive effect2]]'''  
*'''[[Effect::Anxiety suppression]]'''
*'''[[Effect::Cognitive effect3]]'''  
*'''[[Effect::Cognitive euphoria]]'''
*'''[[Effect::Compulsive redosing]]'''
*'''[[Effect::Conceptual thinking]]'''
*'''[[Effect::Creativity enhancement]]'''
*'''[[Effect::Decreased libido]]''' - This is not experienced in all environments, as [[Effect::increased libido]] may also be experienced especially at lower dosage ranges.
*'''[[Effect::Déjà vu]]'''
*'''[[Effect::Depersonalization]]
*'''[[Effect::Derealization]]
*'''[[Effect::Disinhibition]]'''
*'''[[Effect::Dream potentiation]]'''
*'''[[Effect::Ego death]]'''
*'''[[Effect::Immersion enhancement]]'''
*'''[[Effect::Increased music appreciation]]'''
*'''[[Effect::analysis suppression]]
*'''[[Effect::Introspection]]'''
*'''[[Effect::Mania]]''' - This can potentially occur with users who are compulsively and regularly consuming large amounts of this compound. This effect occurs less often on HXE than it does on more stimulating dissociatives such as [[3-MeO-PCP]] or [[2'-Oxo-PCE]].
*'''[[Effect::Memory suppression]]'''
*'''[[Effect::Personal meaning enhancement]]'''
*'''[[Effect::Thought deceleration]]'''
*'''[[Effect::Time distortion]]'''


}}
}}
{{effects/auditory|
{{effects/auditory|
If applicable, a brief paragraph summary of the substance's auditory effects may be included here.


You may select from a list of auditory effects to add below [[Subjective effect index#Auditory effects|here]].
*'''[[Effect::Auditory distortion|Distortions]]'''
 
*'''[[Effect::Auditory hallucinations|Hallucinations]]'''
*'''[[Effect::Auditory effect1]]'''
*'''[[Effect::Auditory suppression|Suppression]]'''
*'''[[Effect::Auditory effect2]]'''


}}
}}
{{effects/multisensory|
If applicable, a brief paragraph summary of the substance's multisensory effects may be included here.


You may select from a list of multisensory effects to add below [[Subjective effect index#Multisensory effects|here]].
{{effects/disconnective|
*'''[[Effect::Tactile disconnection]]'''
*'''[[Effect::Visual disconnection]]''' - This eventually results in HXE's equivalent of the "k-hole" or more specifically, ''[[Visual disconnection#Holes, spaces and voids|holes, spaces and voids]]'' alongside of ''[[Visual disconnection#Structures|structures]]''.
*'''[[Effect::Consciousness disconnection]]'''


*'''[[Effect::Multisensory effect1]]'''
}}
*'''[[Effect::Multisensory effect2]]'''


}}
{{effects/transpersonal|
{{effects/transpersonal|
If applicable, a brief paragraph summary of the substance's transpersonal effects may be included here.
*'''[[Effect::Existential self-realization]]'''
 
*'''[[Effect::Unity and interconnectedness]]'''
You may select from a list of transpersonal effects to add below [[Subjective effect index#Transpersonal effects|here]].
 
*'''[[Effect::Transpersonal effect1]]'''
*'''[[Effect::Transpersonal effect2]]'''


}}
}}
}}
}}
===Experience reports===
===Experience reports===
There are currently {{#ask:[[Category:SUBSTANCE]][[Category:Experience]] | format=count}} experience reports which describe the effects of this substance in our [[experience index]].
There are currently {{#ask:[[Category:HXE]][[Category:Experience]] | format=count}} experience reports which describe the effects of this substance in our [[experience index]].
{{#ask: [[Category:SUBSTANCE]][[Category:Experience]]|format=ul|Columns=1}}
{{#ask: [[Category:HXE]][[Category:Experience]]|format=ul|Columns=1}}
<!--
Additional experience reports can be found here:
Additional experience reports can be found here:
* [https://www.erowid.org/experiences/subs/exp_SUBSTANCE.shtml Erowid Experience Vaults: SUBSTANCE] <!-- Check the link to see if it exists -->
* [https://www.erowid.org/experiences/subs/exp_SUBSTANCE.shtml Erowid Experience Vaults: SUBSTANCE] <!-- Check the link to see if it exists ->
 
-->
==Toxicity and harm potential==
==Toxicity and harm potential==
{{toxicity}}
{{toxicity}}
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It is strongly recommended that one use [[responsible use|harm reduction practices]] when using this substance.
It is strongly recommended that one use [[responsible use|harm reduction practices]] when using this substance.
===Lethal dosage===
===Lethal dosage===
The lethal dosage of HXE is not known. Based on it's effect it could probably be assumed, that it might carry roughly the same risk of death like similar compounds like [[DMXE]] or [[MXPr]].
===Tolerance and addiction potential===
===Tolerance and addiction potential===
As with other nmda receptor antagonists, the chronic use of HXE can be considered [[addiction potential::moderately addictive with a high potential for abuse]] and is capable of producing psychological dependence among certain users.
when addiction has developed, cravings and [[withdrawal effects]] may occur if a person suddenly stops their usage.
tolerance to many of the effects of HXE [[time to full tolerance::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 [[time to half tolerance::3 - 7 days]] for the tolerance to be reduced to half and [[time to zero tolerance::1 - 2 weeks]] to be back at baseline (in the absence of further consumption).
HXE presents cross-tolerance with [[cross-tolerance::all [[dissociative]]s]], meaning that after the consumption of HXE all [[dissociative]]s will have a reduced effect.
===Dangerous interactions===
===Dangerous interactions===
{{DangerousInteractions}}
{{DangerousInteractions}}
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==Legal status==
==Legal status==
{{LegalStub}}
{{LegalStub}}
*'''Switzerland:''' HXE can be considered a specially defined derivative of PCE or O-PCE and is therefore illegal.<ref>{{cite web|url=https://www.admin.ch/opc/de/classified-compilation/20101220/index.html|title=Verordnung des EDI über die Verzeichnisse der Betäubungsmittel, psychotropen Stoffe, Vorläuferstoffe und Hilfschemikalien|publisher=Bundeskanzlei [Federal Chancellery of Switzerland]|access-date=January 1, 2020|language=de}}</ref>
*'''United Kingdom''': HXE is illegal in the United Kingdom.{{citation needed}}
*'''United States''': HXE is not illegal, however, if it is sold with the intention for human consumption (such as in capsules) it becomes illegal to possess under the Federal Analogue Act. This is avoided by placing the label "not for human consumption" on the container of the chemical.{{citation needed}}


==See also==
==See also==
*[[Responsible use]]
*[[Responsible use]]
*[[MXE]]
*[[MXPr]]
*[[Dissociative]]


==External links==
==External links==
{{#l:HXE.svg}}
* https://isomerdesign.com/PiHKAL/explore.php?domain=pk&id=7505&name=HXE
==Literature==
* APA formatted reference


Please see the [[citation formatting guide]] if you need assistance properly formatting citations.
*[https://isomerdesign.com/PiHKAL/explore.php?domain=pk&id=7505&name=HXE HXE (Isomerdesign)]


==References==
==References==
<references />
<references />


[[Category:Psychoactive substance]][[Category:Proofread]][[Category:Approval]]
[[Category:Psychoactive substance]]
[[Category:Proofread]]
[[Category:Approval]]




Please see the [[citation formatting guide]] if you need assistance properly formatting citations.
Please see the [[citation formatting guide]] if you need assistance properly formatting citations.


==References==
[[Category:Psychoactive substance]]
<references />
[[Category:Proofread]]
 
[[Category:Approval]]
[[Category:Psychoactive substance]][[Category:Proofread]][[Category:Approval]]

Latest revision as of 22:13, 5 December 2023

This page has not been fully approved by the PsychonautWiki administrators.

It may contain incorrect information, particularly with respect to dosage, duration, subjective effects, toxicity and other risks. It may also not meet PW style and grammar standards.

Summary sheet: HXE
HXE
Chemical Nomenclature
Common names HXE
Substitutive name 3-HO-2'-Oxo-PCE
Systematic name 2-(Ethylamino)-2-(3-hydroxyphenyl)cyclohexan-1-one
Class Membership
Psychoactive class Dissociative
Chemical class Arylcyclohexylamine
Routes of Administration

WARNING: Always start with lower doses due to differences between individual body weight, tolerance, metabolism, and personal sensitivity. See responsible use section.



Oral
Dosage
Threshold 30 mg
Light 30 - 60 mg
Common 60 - 100 mg
Strong 100 - 130 mg
Heavy 130 mg +
Duration
Total 3 - 8 hours
Onset 20 - 60 minutes
Come up 30 - 60 minutes
Peak 2 - 4 hours
Offset 3 - 6 hours
After effects 1 - 12 hours


Sublingual
Dosage
Threshold 30 mg
Light 30 - 60 mg
Common 60 - 100 mg
Strong 100 - 130 mg
Heavy 130 mg +
Duration
Total 3 - 6 hours
Onset 20 - 60 minutes
Come up 30 - 60 minutes
Peak 2 - 4 hours
Offset 2 - 6 hours
After effects 1 - 12 hours
Insufflated
Dosage
Threshold 20 mg
Light 40 - 20 mg
Common 40 - 70 mg
Strong 70 - 120 mg
Heavy 120 mg +
Duration
Total 3 - 6 hours
Onset 10 - 30 minutes
Come up 20 - 40 minutes
Peak 1.5 - 4 hours
Offset 2 - 4 hours
After effects 2 - 7 hours






DISCLAIMER: PW's dosage information is gathered from users and resources for educational purposes only. It is not a recommendation and should be verified with other sources for accuracy.

Interactions


3-HO-2'-Oxo-PCE (commonly known as HXE) is a novel dissociative substance of the arylcyclohexylamine class that produces ketamine-like dissociative effects when administered. It is structurally related to Methoxetamine, Ketamine and PCE.

Limited data exists about the pharmacological properties, metabolism, and toxicity of HXE in humans, and it has a limited history of human use. It is highly advised to use harm reduction practices if using this substance.

History and culture

HXE first appeared for sale on the online research chemical market in late 2020. However, it has been announced about three years prior where it has been 'hyped' for a long time but was on hold due to synthesis difficulties.[citation needed]

Chemistry

HXE or 2-(Ethylamino)-2-(3-hydroxyphenyl)cyclohexan-1-one is classed as an Arylcyclohexylamine

It is substituted on the cyclohexane ring with an oxygen at the 2' position and a hydroxy group at the 3 position on the phenyl ring. In contrast, MXE is substituted there with a methoxy group.

Pharmacology

Very little is known about the pharmacology about this substance, however as an arylcyclohexamine it is reasonable to assume that it is an NMDA receptor antagonist. NMDA receptors allow for electrical signals to pass between neurons in the brain and spinal column; for the signals to pass, the receptor must be open. Dissociatives close the NMDA receptors by blocking them. This disconnection of neurons leads to loss of feeling, difficulty moving, and eventually an almost identical equivalent of the famous “k-hole.”

Subjective effects

This subjective effects section is a stub.

As such, it is still in progress and may contain incomplete or wrong information.

You can help by expanding or correcting it.

Disclaimer: The effects listed below cite the Subjective Effect Index (SEI), an open research literature based on anecdotal user reports and the personal analyses of PsychonautWiki contributors. As a result, they should be viewed with a healthy degree of skepticism.

It is also worth noting that these effects will not necessarily occur in a predictable or reliable manner, although higher doses are more liable to induce the full spectrum of effects. Likewise, adverse effects become increasingly likely with higher doses and may include addiction, severe injury, or death ☠.

HXE's effects resemble rather the effects of MXPr, MXE, DCK than more chaotic derivatives like O-PCE or MXiPr. Compared to MXE, it has less of a warmth to it and is weaker in its euphoria and clearheadedness, which can roughly be considered equal to MXPr's potency.


Physical effects

Visual effects

Cognitive effects

Disconnective effects

Experience reports

There are currently 0 experience reports which describe the effects of this substance in our experience index.

Toxicity and harm potential

This toxicity and harm potential section is a stub.

As a result, it may contain incomplete or even dangerously wrong information! You can help by expanding upon or correcting it.
Note: Always conduct independent research and use harm reduction practices if using this substance.

The toxicity and long-term health effects of recreational HXE use do not seem to have been studied in any scientific context and the exact toxic dosage is unknown. This is because HXE has very little history of human usage.

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

Lethal dosage

The lethal dosage of HXE is not known. Based on it's effect it could probably be assumed, that it might carry roughly the same risk of death like similar compounds like DMXE or MXPr.

Tolerance and addiction potential

As with other nmda receptor antagonists, the chronic use of HXE can be considered moderately addictive with a high potential for abuse and is capable of producing psychological dependence among certain users. when addiction has developed, cravings and withdrawal effects may occur if a person suddenly stops their usage.

tolerance to many of the effects of HXE 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).

HXE presents cross-tolerance with [[cross-tolerance::all dissociatives]], meaning that after the consumption of HXE all dissociatives will have a reduced effect.

Dangerous interactions

This dangerous interactions section is a stub.

As such, it may contain incomplete or invalid information. You can help by expanding upon or correcting it.

Warning: Many psychoactive substances that are reasonably safe to use on their own can suddenly become dangerous and even life-threatening when combined with certain other substances. The following list provides some known dangerous interactions (although it is not guaranteed to include all of them).

Always conduct independent research (e.g. Google, DuckDuckGo, PubMed) to ensure that a combination of two or more substances is safe to consume. Some of the listed interactions have been sourced from TripSit.

This legality section is a stub.

As such, it may contain incomplete or wrong information. You can help by expanding it.

  • Switzerland: HXE can be considered a specially defined derivative of PCE or O-PCE and is therefore illegal.[1]
  • United Kingdom: HXE is illegal in the United Kingdom.[citation needed]
  • United States: HXE is not illegal, however, if it is sold with the intention for human consumption (such as in capsules) it becomes illegal to possess under the Federal Analogue Act. This is avoided by placing the label "not for human consumption" on the container of the chemical.[citation needed]


See also


References

  1. "Verordnung des EDI über die Verzeichnisse der Betäubungsmittel, psychotropen Stoffe, Vorläuferstoffe und Hilfschemikalien" (in Deutsch). Bundeskanzlei [Federal Chancellery of Switzerland]. Retrieved January 1, 2020. 


Please see the citation formatting guide if you need assistance properly formatting citations.