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Part I Class A
Section 1(a): Explicitly named Class A substances
Section 1(b): Tryptamines, generic
Section 1(ba): Phenethylamines, explicitly named
Section 1(c): Phenethylamines, generic
Section 1(d): Fentanyls, generic
Section 1(e): Pethedines, generic
Section 1(f):
N
-Benzyl phenethylamines, generic
Section 2 to 6: Analogues, various, defined
All sections
Part II Class B
Section 1(a): Explicitly named Class B substances
Section 1(aa): Cathinones, generic
Section 1(ab): Quasi-cathinones, generic
Section 1(ac): Pipradrol analogues, generic
Section 1(b): Barbiturates, generic
Section 1(c): Cannabinoids, nonclassical, generic
Section 1(d): Aryl cyclohexylamines, generic
Section 1(e): Fused ring arylethylamines, generic
Section 2, 2A, 3 and 4: Analogues, various, defined
All sections
Part III Class C
Section 1(a): Explicitly named Class C substances
Section 1(b): Steroids, explicitly named
Section 1(c): Steroids, generic
Section 1(ca): Benzyl and phenyl piperazines, generic
Section 1(d): Analogues, various, defined
Section 1(e): Explicitly named Class C substances
Section 2 to 4: Analogues, various, defined
All sections
Drug precursors
Annex I Category 1: Explicitly named substances
Annex I Category 2: Explicitly named substances
Annex I Category 3: Explicitly named substances
Annex II Explicitly named substances
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Drugs Subject to Temporary Control
Effective 10 Jun 2013,
S.I. 2013/1294
added, for one year’s duration:
1.
The following substances, namely—
Effective 10 Jun 2013,
S.I. 2013/1294
added, for one year’s duration:
2-(4-Iodo-2,5-dimethoxyphenyl)-
N
-[(2-methoxyphenyl)methyl]ethanamine
EU: Substances Substances
2-(4-Iodo-2,5-dimethoxy)-
N
-(2-methoxybenzyl) phenethylamine
US: CSA Schedule I Section h Subsection 4
2-(4-Iodo-2,5-dimethoxyphenyl)-
N
-(2-methoxybenzyl)ethanamine
US: [proposed] CSA Schedule I Section d Subsection 48
2-(4-Iodo-2,5-dimethoxyphenyl)-
N
-(2-methoxybenzyl)ethanamine
UK: Currently at MDA Part I Class A Section 1(f)
2-(4-Iodo-2,5-dimethoxyphenyl)-
N
-[(2-methoxyphenyl)methyl]ethanamine
⇒
PubChem
:
10251906
;
ChemSpider
:
8427392
;
Bluelight
:
25I-NBOMe
;
Drugs Forum
:
25I-NBOMe
;
Erowid
:
25I-NBOMe
;
Wikipedia
:
25I-NBOMe
Effective 10 Jun 2013,
S.I. 2013/1294
added, for one year’s duration:
2-(4-Bromo-2,5-dimethoxyphenyl)-
N
-[(2-methoxyphenyl)methyl]ethanamine
US: CSA Schedule I Section h Subsection 6
2-(4-Bromo-2,5-dimethoxyphenyl)-
N
-(2-methoxybenzyl)ethanamine
US: [proposed] CSA Schedule I Section d Subsection 50
2-(4-Bromo-2,5-dimethoxyphenyl)-
N
-(2-methoxybenzyl)ethanamine
UK: Currently at MDA Part I Class A Section 1(f)
2-(4-Bromo-2,5-dimethoxyphenyl)-
N
-[(2-methoxyphenyl)methyl]ethanamine
⇒
PubChem
:
9977044
;
ChemSpider
:
8152636
;
Bluelight
:
25B-NBOMe
;
Drugs Forum
:
25B-NBOMe
;
Wikipedia
:
25B-NBOMe
Effective 10 Jun 2013,
S.I. 2013/1294
added, for one year’s duration:
2-(2,5-Dimethoxy-4-methylphenyl)-
N
-[(2-methoxyphenyl)methyl]ethanamine
UK: Currently at MDA Part I Class A Section 1(f)
2-(2,5-Dimethoxy-4-methylphenyl)-
N
-[(2-methoxyphenyl)methyl]ethanamine
⇒
ChemSpider
:
29341727
;
Drugs Forum
:
25D-NBOMe
;
Wikipedia
:
25D-NBOMe
Effective 10 Jun 2013,
S.I. 2013/1294
added, for one year’s duration:
2-(4-Chloro-2,5-dimethoxyphenyl)-
N
-[(2-methoxyphenyl)methyl]ethanamine
US: CSA Schedule I Section h Subsection 5
2-(4-Chloro-2,5-dimethoxyphenyl)-
N
-(2-methoxybenzyl)ethanamine
US: [proposed] CSA Schedule I Section d Subsection 49
2-(4-Chloro-2,5-dimethoxyphenyl)-
N
-(2-methoxybenzyl)ethanamine
UK: Currently at MDA Part I Class A Section 1(f)
2-(4-Chloro-2,5-dimethoxyphenyl)-
N
-[(2-methoxyphenyl)methyl]ethanamine
⇒
PubChem
:
46856354
;
ChemSpider
:
24583389
;
Bluelight
:
25C-NBOMe
;
Drugs Forum
:
25C-NBOMe
;
Erowid
:
25C-NBOMe
;
Wikipedia
:
25C-NBOMe
Effective 10 Jun 2013,
S.I. 2013/1294
added, for one year’s duration:
2.
The following substances, namely—
Effective 10 Jun 2013,
S.I. 2013/1294
added, for one year’s duration:
1-(Benzofuran-5-yl)-propan-2-amine
and its
N
-methyl derivatives
UK: Currently at MDA Part II Class B Section 1(e)
1-(Benzofuran-5-yl)-propan-2-amine
⇒
PubChem
:
9837232
;
ChemSpider
:
8012953
;
Drugs Forum
:
5-APB
;
Wikipedia
:
5-APB
Effective 10 Jun 2013,
S.I. 2013/1294
added, for one year’s duration:
1-(Benzofuran-6-yl)-propan-2-amine
and its
N
-methyl derivatives
UK: Currently at MDA Part II Class B Section 1(e)
1-(Benzofuran-6-yl)-propan-2-amine
⇒
PubChem
:
9794343
;
ChemSpider
:
7970110
;
Bluelight
:
6-APB
;
Drugs Forum
:
6-APB
;
Erowid
:
6-APB
;
Wikipedia
:
6-APB
Effective 10 Jun 2013,
S.I. 2013/1294
added, for one year’s duration:
1-(2,3-Dihydro-1-benzofuran-5-yl)-propan-2-amine
and its
N
-methyl derivatives
UK: Currently at MDA Part II Class B Section 1(e)
1-(2,3-Dihydro-1-benzofuran-5-yl)-propan-2-amine
⇒
PubChem
:
192601
;
ChemSpider
:
167143
;
Drugs Forum
:
5-APDB
;
Wikipedia
:
5-APDB
Effective 10 Jun 2013,
S.I. 2013/1294
added, for one year’s duration:
1-(2,3-Dihydro-1-benzofuran-6-yl)-propan-2-amine
and its
N
-methyl derivatives
UK: Currently at MDA Part II Class B Section 1(e)
1-(2,3-Dihydro-1-benzofuran-6-yl)-propan-2-amine
⇒
PubChem
:
192599
;
ChemSpider
:
167141
;
Wikipedia
:
6-APDB
Effective 10 Jun 2013,
S.I. 2013/1294
added, for one year’s duration:
1-(1
H
-Indol-5-yl)-1-methylethylamine
EU: Substances Substances
5-(2-Aminopropyl)indole
UK: Currently at MDA Part II Class B Section 1(e)
1-(1
H
-Indol-5-yl)-1-methylethylamine
⇒
PubChem
:
55253543
;
ChemSpider
:
25991467
;
Erowid
:
5-IT (5-(2-Aminopropyl)indole)
;
Wikipedia
:
5-(2-Aminopropyl)indole
Effective 10 Jun 2013,
S.I. 2013/1294
added, for one year’s duration:
1-(1
H
-Indol-6-yl)-1-methylethylamine
UK: Currently at MDA Part II Class B Section 1(e)
1-(1
H
-Indol-6-yl)-1-methylethylamine
Effective 10 Jun 2013,
S.I. 2013/1294
added, for one year’s duration:
3.
Any stereoisomeric form of a substance specified in paragraph 1 or 2.
Effective 10 Jun 2013,
S.I. 2013/1294
added, for one year’s duration:
4.
Any salt of a substance specified in any of paragraphs 1 to 3.
Effective 10 Jun 2013,
S.I. 2013/1294
added, for one year’s duration:
5.
Any preparation or other product containing a substance specified in any of paragraphs 1 to 4.
11 March 2016 ·
·
Isomer Design