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C6395

Supelco

Cannabidiol solution

1.0 mg/mL in methanol, analytical standard, for drug analysis

Synonyme(s) :

CBD

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About This Item

Formule empirique (notation de Hill):
C21H30O2
Numéro CAS:
13956-29-1
Poids moléculaire :
314.46
Numéro CE :
200-659-6
Numéro MDL:
MFCD00869597
Code UNSPSC :
41116107
ID de substance PubChem :
329775124
Nomenclature NACRES :
NA.24

Qualité

analytical standard

Niveau de qualité

200

Concentration

1.0 mg/mL in methanol

Technique(s)

HPLC: suitable
gas chromatography (GC): suitable

Application(s)

pharmaceutical (small molecule)

Format

single component solution

Température de stockage

2-8°C

Chaîne SMILES 

CCCCCc1cc(O)c([C@@H]2C=C(C)CC[C@H]2C(C)=C)c(O)c1

InChI

1S/C21H30O2/c1-5-6-7-8-16-12-19(22)21(20(23)13-16)18-11-15(4)9-10-17(18)14(2)3/h11-13,17-18,22-23H,2,5-10H2,1,3-4H3/t17-,18+/m0/s1

Clé InChI

QHMBSVQNZZTUGM-ZWKOTPCHSA-N

Informations sur le gène

human ... CNR1(1268) , CNR2(1269)
rat ... Cnr1(25248)

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Catégories apparentées

Description générale

Cannabidiol belongs to the group of active cannabinoids, available in neutral form, derived from Cannabis species and is available as a main component of illicit drugs such as hashish (cannabis resin) and marijuana (herbal cannabis).

Application

Cannabidiol is used as an analytical reference standard for the quantification of the analyte in hashish drug samples and plasma samples using chromatography techniques.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Pictogrammes

FlameSkull and crossbonesHealth hazard
GHS02,GHS06,GHS08

Mention d'avertissement

Danger

Classification des risques

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Flam. Liq. 2 - STOT SE 1

Organes cibles

Eyes,Central nervous system

Code de la classe de stockage

3 - Flammable liquids

Classe de danger pour l'eau (WGK)

WGK 2

Point d'éclair (°F)

49.5 °F - closed cup

Point d'éclair (°C)

9.7 °C - closed cup

Équipement de protection individuelle

Eyeshields, Faceshields, Gloves

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Certificats d'analyse (COA)

Lot/Batch Number
0000320402
SLCR0734
SLCP0160
SLCH1429
SLCC9048

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Consulter la Bibliothèque de documents

Simultaneous separation and identification of hashish constituents by coupled liquid chromatography-mass spectrometry (HPLC-MS)
Rustichelli.C, et al.
Chromatographia, 43(3-4), 129-134 (1996)
Development of a simple and sensitive HPLC?UV method for the simultaneous determination of cannabidiol and ?9-tetrahydrocannabinol in rat plasma
Zgair A, et al.
Journal of Pharmaceutical and Biomedical Analysis, 114(3-4), 145-151 (2015)
Maiko Tsuchiya et al.
International journal of molecular sciences, 20(24) (2019-12-15)
Bone metabolism is strictly regulated, and impaired regulation caused by hormonal imbalances induces systemic bone loss. Local bone loss caused by tumor invasion into bone is suggested to be induced by the generation of cytokines, which affect bone metabolism, by
R G Pertwee
British journal of pharmacology, 153(2), 199-215 (2007-09-11)
Cannabis sativa is the source of a unique set of compounds known collectively as plant cannabinoids or phytocannabinoids. This review focuses on the manner with which three of these compounds, (-)-trans-delta9-tetrahydrocannabinol (delta9-THC), (-)-cannabidiol (CBD) and (-)-trans-delta9-tetrahydrocannabivarin (delta9-THCV), interact with cannabinoid
Alline Cristina Campos et al.
Psychopharmacology, 226(1), 13-24 (2012-09-26)
Cannabidiol (CBD) is a non-psychotomimetic constituent of Cannabis sativa plant that promotes antianxiety and anti-panic effects in animal models after acute systemic or intra-dorsal periaqueductal gray (DPAG) administration. However, the effects of CBD repeated administration, and the possible mechanisms involved
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