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Documentos Principais

C6395

Supelco

Cannabidiol solution

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

Sinônimo(s):

CBD

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About This Item

Fórmula empírica (Notação de Hill):
C21H30O2
Número CAS:
Peso molecular:
314.46
Número CE:
Número MDL:
Código UNSPSC:
41116107
ID de substância PubChem:
NACRES:
NA.24

grau

analytical standard

Nível de qualidade

concentração

1.0 mg/mL in methanol

técnica(s)

HPLC: suitable
gas chromatography (GC): suitable

aplicação(ões)

pharmaceutical (small molecule)

Formato

single component solution

temperatura de armazenamento

2-8°C

cadeia de caracteres 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

chave InChI

QHMBSVQNZZTUGM-ZWKOTPCHSA-N

Informações sobre genes

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Descrição geral

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).

Aplicação

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.

Palavra indicadora

Danger

Classificações de perigo

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

Órgãos-alvo

Eyes,Central nervous system

Código de classe de armazenamento

3 - Flammable liquids

Classe de risco de água (WGK)

WGK 2

Ponto de fulgor (°F)

49.5 °F - closed cup

Ponto de fulgor (°C)

9.7 °C - closed cup

Equipamento de proteção individual

Eyeshields, Faceshields, Gloves


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Certificados de análise (COA)

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Visite a Biblioteca de Documentos

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
Javier Fernández-Ruiz et al.
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

Artigos

-THC solution, 1.0 mg/mL in methanol, ampule of 1 mL, certified reference material; Cannabichromene solution, 1.0 mg/mL in methanol, ampule of 1 mL, certified reference material

Tetrahydrocannabinolic acid A solution, 1.0 mg/mL in acetonitrile, ampule of 1 mL, certified reference material.

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