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MY'STORY

The MOVE Fire

This is a personal recollection on the Move fire on May 13, 1985 Philadelphia police fired thousands of rounds at the MOVE house, city officials approved dropping an explosive device on the roof, the resulting fire was allowed to burn, 11 people—including five children—died, and 61 homes were destroyed. Philadelphia City Council later called it a “brutal attack carried out by the City of Philadelphia on its own citizens” and acknowledged that no individual faced criminal consequences for the bombing. One timeline correction worth preserving for the BHP record: the major previous MOVE-police confrontation was August 8, 1978, about seven years before the bombing, not a year or two earlier. Officer James Ramp was killed, other police and firefighters were wounded, nine MOVE members were later convicted, and television cameras recorded police beating Delbert Africa during his arrest. The 1985 MOVE Commission later specifically criticized city planners for failing to adequately use lessons from that 1978 confrontation. And that actually strengthens the point you’re making: 1985 did not happen without precedent or institutional memory. There had already been a deadly confrontation with MOVE, years of conflict, negotiations and police involvement before Osage Avenue.

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BLACK FACTS
The Truths They Never Taught You...

Katherine Johnson — Mathematics to the Moon

Katherine Johnson’s mathematical calculations helped guide some of America’s most important early space missions while she confronted the racial and gender barriers faced by Black women in twentieth-century America.

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Wikipedia

Methoxypropane

Methoxypropane
Names
Preferred IUPAC name
1-Methoxypropane
Other names
Propane, 1-methoxy-
methyl propyl ether
Metopryl
Neothyl
propane, 1-methoxy
methyl n-propyl ether
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.008.327 Edit this at Wikidata
EC Number
  • 209-158-7
RTECS number
  • KO2280000
UNII
UN number 2612
  • InChI=1S/C4H10O/c1-3-4-5-2/h3-4H2,1-2H3 checkY
    Key: VNKYTQGIUYNRMY-UHFFFAOYSA-N checkY
  • InChI=1/C4H10O/c1-3-4-5-2/h3-4H2,1-2H3
  • O(CCC)C
Properties
C4H10O
Molar mass 74.12
Density 0.7356 g/cm3
Boiling point 38.8 °C (101.8 °F; 311.9 K)
30.5 g/L
1.35837 (14.3 °C)
Viscosity 0.3064 cP (0.3 °C)
Pharmacology
inhalation
Hazards
NFPA 704 (fire diamond)
NFPA 704 four-colored diamondHealth 0: Exposure under fire conditions would offer no hazard beyond that of ordinary combustible material. E.g. sodium chlorideFlammability 3: Liquids and solids that can be ignited under almost all ambient temperature conditions. Flash point between 23 and 38 °C (73 and 100 °F). E.g. gasolineInstability 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g. liquid nitrogenSpecial hazards (white): no code
0
3
0
Flash point < −20 °C (−4 °F; 253 K)
Explosive limits 1.9–11.8%
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
X markN verify (what is checkYX markN ?)

Methoxypropane, or methyl propyl ether, is an ether once used as a general anaesthetic.[1] It is a clear colorless flammable liquid with a boiling point of 38.8 °C.[2]

Marketed under the trade names Metopryl and Neothyl, methoxypropane was used as an alternative to diethyl ether because of its greater potency. Its use as an anaesthetic has since been supplanted by modern halogenated ethers which are much less flammable.

References

[edit]
  1. ^ White, Mary Louise T.; Shane, Sylvan M.; Krantz, John C., Jr. "Anesthesia. XXI. Propyl methyl ether as an inhalation anesthetic in man", Anesthesiology, (1946), 7, 663-7.
  2. ^ Merck Index, 11th edition, 6031.


Source: Wikipedia. Article content is retrieved live through the MediaWiki API.

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Wikipedia

Methoxypropane

Methoxypropane, or methyl propyl ether, is an ether once used as a general anaesthetic. It is a clear colorless flammable liquid with a boiling point of 38.8 °C. Marketed under the trade names Metopryl and Neothyl, methoxypropane was used as an alternative to diethyl ether because of its greater potency. Its use as an anaesthetic has since been supplanted by modern halogenated ethers which are much less flammable.

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Wikipedia

C4H10O

The molecular formula C4H10O may refer to: Butanols 1-Butanol (n-Butanol) 2-Butanol (sec-Butanol) Isobutanol (2-methylpropan-1-ol) tert-Butyl alcohol (tert-Butanol, 2-methylpropanol) Ethers: Diethyl ether (ethoxyethane) Methoxypropane (methyl propyl ether or 1-methoxypropane) Methyl isopropyl ether (isopropyl methyl ether or 2-methoxypropane)

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Wikipedia

Sodium thiopental

Sodium thiopental, also known as thiopental sodium or thiopentone and sold under the brand name Pentothal, is a rapid-onset short-acting barbiturate general anesthetic. It is the thiobarbiturate analog of pentobarbital, and an analog of thiobarbital. Sodium thiopental is a therapeutic alternative on the World Health Organization's List of Essential Medicines. It was the first of three drugs administered during most lethal injections in the United States until the US division of Hospira objected and stopped manufacturing the drug for this purpose in 2011, and the European Union additionally banned the export of the drug for this purpose. Although thiopental abuse carries a dependency risk, its recreational use is rare. Sodium thiopental is well-known in popular culture, especially under the name "sodium pentothal," as a "truth serum," although its efficacy in this role is questioned.

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Wikipedia

Valerian (herb)

Valerian (Valeriana officinalis) is an herbaceous perennial flowering plant in the family Caprifoliaceae, native to Europe and southwestern Asia. It is the type species of the genus Valeriana.

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TOPIC OF THE DAY

Greenwood / Black Wall Street

Before the 1921 destruction of Tulsa’s Greenwood District, Black residents had created a remarkable center of business and community life. The district included stores, professional offices, entertainment venues and homes owned by Black citizens. Understanding Greenwood means learning what was built—not only what was burned.

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TRIVIA QUESTION OF THE DAY

Which heavyweight champion was known as the “Brown Bomber”?

Joe Louis.