C18-Ceramide-d₇

Cat. No.: HY-100355S1 Purity: ≥99.0%: FAQs
Data Sheet
SDS

COA
Handling Instructions Technical Support

For research use only. We do not sell to patients.

C18-Ceramide-d<sub>7</sub> Chemical Structure

C18-Ceramide-d₇ Chemical Structure

Size	Stock	Quantity
Solution
500 μg (1.75 mM * 500 μL in Methanol:Chloroform (10:90))	Get quote 2-4 weeks 2-4 weeks 2-4 weeks	Estimated Time of Arrival: December 31
Liquid
1 mg	Get quote	Estimated Time of Arrival: December 31
5 mg	Get quote	Estimated Time of Arrival: December 31

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Based on 1 publication(s) in Google Scholar

Other Forms of C18-Ceramide-d₇:

C18-Ceramide Get quote
C18-Ceramide-d₃ Get quote

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Biological Activity
Purity & Documentation
References
Customer Review

Molecular Weight	573.00
Formula	C₃₆H₆₄D₇NO₃
CAS No.	1840942-14-4
Unlabeled CAS	2304-81-6
Appearance	Liquid
Color	Colorless to light yellow
SMILES	CCCCCCCCCCCCCCCCCC(N[C@@H](CO)[C@H](O)/C=C/CCCCCCCCCCC([2H])([2H])C([2H])([2H])C([2H])([2H])[2H])=O
Shipping	Room temperature in continental US; may vary elsewhere.
Storage	Solution, -20°C, 2 years
Solvent & Solubility	In Vitro: Ethanol : 10 mg/mL (17.45 mM; Need ultrasonic and warming) Molarity Calculator Dilution Calculator Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol) Mass = Concentration × Volume × Molecular Weight * Concentration _(start) × Volume _(start) = Concentration _(final) × Volume _(final) This equation is commonly abbreviated as: C₁V₁ = C₂V₂ Concentration _(start) C1 × Volume _(start) V1 = Concentration _(final) C2 × Volume _(final) V2 In Vivo Dissolution Calculator Please enter the basic information of animal experiments: Dosage mg/kg Animal weight (per animal) g Dosing volume (per animal) μL Number of animals Recommended: Prepare an additional quantity of animals to account for potential losses during experiments. Calculation results: Working solution concentration: mg/mL
Purity & Documentation	Purity: ≥99.0% Select Batch: Data Sheet (260 KB) SDS (251 KB) COA (239 KB) Handling Instructions (2659 KB)
References	[1]. Russak EM, et al. Impact of Deuterium Substitution on the Pharmacokinetics of Pharmaceuticals. Ann Pharmacother. 2019;53(2):211-223. [Content Brief]

Complete Stock Solution Preparation Table

* Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month. When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.

Optional Solvent	Concentration Solvent Mass	1 mg	5 mg	10 mg	25 mg

Ethanol	1 mM	1.7452 mL	8.7260 mL	17.4520 mL	43.6300 mL
	5 mM	0.3490 mL	1.7452 mL	3.4904 mL	8.7260 mL
	10 mM	0.1745 mL	0.8726 mL	1.7452 mL	4.3630 mL
	15 mM	0.1163 mL	0.5817 mL	1.1635 mL	2.9087 mL