This is a working overview of DMSO stock, written for readers who want more than a one-paragraph summary but less than a textbook.
Reviewed 2026-08-01. Anything still debated is marked as such rather than presented as settled.
Laboratory identification of SR9009 typically relies on chromatographic separation coupled to mass spectrometry, often with ultraviolet detection as a secondary check. Nuclear magnetic resonance spectroscopy can confirm molecular structure when a reference standard is available. Because many suppliers sell the compound as a research chemical, independent identity testing is important for experimental reproducibility. A single retention time is not sufficient proof of identity, especially when related compounds may be present. Purity assessments usually report a percentage based on area normalization.
SR9009 is generally described as poorly soluble in water and more soluble in organic solvents such as dimethyl sulfoxide and ethanol. Stock solutions are commonly prepared in an organic solvent before dilution into an aqueous buffer or vehicle. Precipitation can occur if the organic fraction is reduced too quickly or if the final concentration exceeds the compound's solubility limit. Sonication or gentle warming may aid dissolution in some protocols, but excessive heat can promote degradation. Container material and pH can also influence observed solubility.
For long-term storage, SR9009 is typically kept as a solid at low temperature, protected from moisture and light. Desiccated conditions limit hydrolysis, while opaque containers reduce photochemical breakdown. Solutions are less stable than solids and are often stored frozen in aliquots to avoid repeated freeze-thaw cycles. Stability data are not standardized across all suppliers, so users should rely on certificate-of-analysis information when available. Degradation may appear as color change, precipitate, or decreased chromatographic purity.
In laboratory settings, SR9009 is commonly identified by its molecular structure and its interaction with REV-ERB receptors. Vendors may list it under synonyms such as Stenabolic or REV-ERB agonist, but those names do not define purity or identity. Analytical confirmation typically uses high-performance liquid chromatography with ultraviolet detection or liquid chromatography–mass spectrometry. A reference standard is needed to compare retention time and mass spectrum, because the compound can be confused with related research chemicals.
Handling practices for SR9009 focus on minimizing degradation and contamination. The solid is generally stored desiccated at or below -20 °C, protected from light and moisture. Stock solutions are often prepared in dimethyl sulfoxide or ethanol, then aliquoted to avoid repeated freeze–thaw cycles. Aqueous solubility is low, so formulations for animal studies may require cosolvents or suspending agents. Personnel should follow institutional chemical safety procedures, because toxicological data for humans are incomplete.
| Property | Value | Notes |
|---|---|---|
| Appearance | White to off-white powder | Visual inspection is not sufficient for identity. |
| Solubility | Soluble in DMSO and ethanol | Low solubility in water; stock solutions use organic solvent. |
| Storage | -20°C, desiccated, protected from light | Limits hydrolysis and photodegradation. |
| Analytical method | HPLC-UV/MS | Used for identity and purity assessment. |
| Synonyms | SR9009, Stenabolic | Naming varies by supplier. |
SR9009 is a synthetic small molecule studied as an agonist of the nuclear receptors REV-ERBα and REV-ERBβ. These receptors help regulate circadian rhythms and metabolic gene expression. In laboratory experiments, SR9009 binds these receptors and alters transcription of genes involved in lipid handling, glucose metabolism, and mitochondrial function. It is not a naturally occurring compound and has no approved therapeutic use. Research interest stems from its ability to modify energy metabolism in cells and animal models.
In rodent studies, SR9009 has been reported to increase mitochondrial content in skeletal muscle and improve exercise endurance under some conditions. These findings led to popular descriptions such as an exercise mimetic, although that term oversimplifies the biology. Effects vary by dose, timing, tissue, and model. The compound's influence on circadian pathways means that time of administration can matter in experiments. Whether similar metabolic changes occur in humans remains largely unexplored in controlled published trials.
== External links == Chronological History of the Development of Insecticides and Control Equipment from 1854 through 1954 Background on History of Pesticide Use and Regulation in the United States, Part Two (PDF, 54 kB). The Value of Fungicides in U.S. Crop Production, (PDF, 1.1 MB)
=== Ribosomal proteins with roles in signaling === Two 40S ribosomal proteins (RACK1 and RPS6 (or eS6)) have been implicated in cellular signaling: RACK1, first described as the receptor of activated protein kinase C (PKC), is an integral component of the eukaryotic ribosome and is located at the back of the head. It may link signal-transduction pathways directly to the ribosome though it also has a role in multiple translational processes that appear unrelated (reviewed in ). Ribosomal protein eS6 is located at the right foot of the 40S subunit and is phosphorylated in response to mammalian target of rapamycin (mTOR) signaling.
== Further reading == "Bernie Sanders Explains... Why Americans Are Furious at the Democrats: The Nation Interview [by John Nichols]", The Nation, vol. 321, no. 4 (November 2025), pp. 30–34. "[T]he [Democratic] party is saying, '[W]e can't support [Zohran Mamdani, running for New York City mayor] because he is saying what 75 percent of Democrats say about Israel: No more money for Netanyahu.' [p. 32.] [T]he money people decide who the candidates are... [p. 33.] A few years ago ... a poll [showed that] [a]lmost 60 percent of the people said [they] were better off 50 years ago. [p. 34.]" Chiasson, Dan (2026). Bernie for Burlington: The Rise of the People's Politician. New York: Knopf. ISBN 978-0-59331-749-5. Rall, Ted (2016). Bernie. New York: Hollowbrook Publishing. ISBN 978-1-60980-698-9. Rice, Tom W. (1985). "Who Votes for a Socialist Mayor?: The Case of Burlington, Vermont". Polity. 17 (4): 795–806. doi:10.2307/3234575. ISSN 0032-3497. JSTOR 3234575. OCLC 5546248357. S2CID 153889856. Rosenfeld, Steven (1992). Making History in Vermont: The Election of a Socialist to Congress. Wakefield, NH: Hollowbrook Publishing. ISBN 978-0-89341-698-0. LCCN 91034055. OCLC 24468446. OL 1553980M. Soifer, Steven (1991). The Socialist Mayor: Bernard Sanders in Burlington, Vermont. Westport, CN: Praeger. ISBN 978-0-89789-219-3. LCCN 90048954. OCLC 22491683. OL 1887682M.
Sources: en.wikipedia.org
Perchlorate was detected in Martian soil at the level of ~0.6% by weight. It was shown that at the Phoenix landing site it was present as a mixture of 60% Ca(ClO4)2 and 40% Mg(ClO4)2. These salts, formed from perchlorates, act as antifreeze and substantially lower the freezing point of water. Based on the temperature and pressure conditions on present-day Mars at the Phoenix lander site, conditions would allow a perchlorate salt solution to be stable in liquid form for a few hours each day during the summer. The possibility that the perchlorate was a contaminant brought from Earth was eliminated by several lines of evidence. The Phoenix retro-rockets used ultra pure hydrazine and launch propellants consisting of ammonium perchlorate or ammonium nitrate. Sensors on board Phoenix found no traces of ammonium nitrate, and thus the nitrate in the quantities present in all three soil samples is indigenous to the Martian soil. Perchlorate is widespread in Martian soils at concentrations between 0.5 and 1%. At such concentrations, perchlorate could be an important source of oxygen, but it could also become a critical chemical hazard to astronauts. In 2006, a mechanism was proposed for the formation of perchlorates that is particularly relevant to the discovery of perchlorate at the Phoenix lander site. It was shown that soils with high concentrations of chloride converted to perchlorate in the presence of titanium dioxide and sunlight/ultraviolet light. The conversion was reproduced in the lab using chloride-rich soils from Death Valley.
=== 4 November === The SAF claimed to have shot down a drone near Babanusa, while the RSF claimed to have shot down an Ilyushin warplane over the same city. The SAF acknowledged the loss of a cargo aircraft in the city along with its entire crew, but blamed the incident on a technical malfunction.
Acute Care Hospital Ambulatory Care Ambulatory Surgery Center Assisted Living Behavioral Health Clinical Laboratory Critical Access Hospital Dentistry DMEPOS Home Care (Private Duty) Home Health Home Infusion Therapy Hospice Office-Based Surgery Palliative Care PCAB (Compounding) Pharmacy Renal Dialysis Sleep The accreditation process for laboratories follows a two-year cycle, all other programs follow a three-year cycle. In early 2013, ACHC moved to headquarters in Cary, North Carolina. It welcomed its new CEO, José Domingos, and it launched its Behavioral Health Program.
Sources: en.wikipedia.org
Liquid chromatography with mass spectrometry is a common approach. Ultraviolet detection and nuclear magnetic resonance can support identification when suitable standards are available.
The solid is generally kept cold, dry, and protected from light. Solutions are often frozen in single-use aliquots to reduce repeated freeze-thaw cycles.
It indicates a material sold for laboratory study, not for human use. The label does not guarantee pharmaceutical purity, sterility, or regulatory approval.
Liquid chromatography–mass spectrometry is common for identity and purity checks. High-performance liquid chromatography with ultraviolet detection can also be used. Both methods require a suitable reference standard.