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C6395

Supelco

Cannabidiolo

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

Sinonimo/i:

CBD

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About This Item

Formula empirica (notazione di Hill):
C21H30O2
Numero CAS:
13956-29-1
Peso molecolare:
314.46
Numero CE:
200-659-6
Numero MDL:
MFCD00869597
Codice UNSPSC:
41116107
ID PubChem:
329775124
NACRES:
NA.24

Grado

analytical standard

Livello qualitativo

200

Concentrazione

1.0 mg/mL in methanol

tecniche

HPLC: suitable
gas chromatography (GC): suitable

applicazioni

pharmaceutical (small molecule)

Formato

single component solution

Temperatura di conservazione

2-8°C

Stringa SMILE

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
QHMBSVQNZZTUGM-ZWKOTPCHSA-N

Informazioni sul gene

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

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Categorie correlate

Descrizione generale

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).

Applicazioni

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.

Avvertenze

Danger

Indicazioni di pericolo

H225,H301 + H311 + H331,H370

Classi di pericolo

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

Organi bersaglio

Eyes,Central nervous system

Codice della classe di stoccaggio

3 - Flammable liquids

Classe di pericolosità dell'acqua (WGK)

WGK 2

Punto d’infiammabilità (°F)

49.5 °F - closed cup

Punto d’infiammabilità (°C)

9.7 °C - closed cup

Dispositivi di protezione individuale

Eyeshields, Faceshields, Gloves

Scegli una delle versioni più recenti:

Certificati d'analisi (COA)

Lot/Batch Number
SLCH1429
SLCC9048
SLBW8466
SLBR7880V
SLBM6755V

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Supelco

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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)
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)
Shimon Ben-Shabat et al.
Journal of medicinal chemistry, 49(3), 1113-1117 (2006-02-03)
Cannabidiol (CBD) and cannabidiol dimethyl hephtyl (CBD-DMH) were hydrogenated to give four different epimers. The new derivatives were evaluated for their ability to modulate the production of reactive oxygen intermediates (ROI), nitric oxide (NO), and tumor necrosis factor (TNF-alpha) by
Amir Englund et al.
Journal of psychopharmacology (Oxford, England), 27(1), 19-27 (2012-10-09)
Community-based studies suggest that cannabis products that are high in Δ⁹-tetrahydrocannabinol (THC) but low in cannabidiol (CBD) are particularly hazardous for mental health. Laboratory-based studies are ideal for clarifying this issue because THC and CBD can be administered in pure
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British journal of clinical pharmacology, 75(2), 323-333 (2012-05-26)
Cannabidiol (CBD) is a phytocannabinoid with therapeutic properties for numerous disorders exerted through molecular mechanisms that are yet to be completely identified. CBD acts in some experimental models as an anti-inflammatory, anticonvulsant, anti-oxidant, anti-emetic, anxiolytic and antipsychotic agent, and is
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