17 Years Developing Chemtrails – Biochemist Created Aerial Pharmaceuticals

spraying
serotonin uptake re-inhibitors- blood brain barriers

spraying Boron poisoning
Am J Emerg Med. 1992 Nov;10(6):545-7.
Fatal ingestion of boric acid in an adult.
Restuccio A1, Mortensen ME, Kelley MT.
Author information
Abstract
A 45-year-old white man ingested approximately two cups of boric acid crystals dissolved in water in a suicide attempt. Nausea, vomiting, greenish diarrhea, and dehydration occurred shortly thereafter. Two days later, he presented to the hospital with hypotension, metabolic acidosis, oliguric renal failure, a generalized erythematous rash, and several superficial skin abrasions. His condition failed to improve despite intravenous fluids and vasopressors. He later developed atrial fibrillation with a rapid ventricular response and could not be converted to a sinus rhythm. This rhythm deteriorated to electromechanical dissociation, and the patient died 17 hours after admission. The urine and whole blood boric acid concentrations approximately 52 hours after ingestion were 160 and 42 mg/dL, respectively. These results are equivalent to urine and blood boron concentrations of 28 and 7 mg/dL, respectively. A postmortem urine boron concentration was 29.4 mg/dL. The autopsy report listed boron toxicity as the cause of death. This is the only adult reported to die from acute boric acid ingestion in recent years and may be atypical since the patient was untreated for 3 days and presented with dehydration and renal function impairment. This case suggests that lack of adequate urine flow and dehydration increases the risk of boron toxicity.

PMID: 1388380
[Indexed for MEDLINE]

Boron is a Borate compound.
Report a Poisoning
Symptoms of Poisoning with Borate Compounds
Find Products Containing this Chemical
- Irritation of skin and respiratory tract.
- The gastrointestinal tract , skin vascular system and brain are the principal organs and tissues affected.
- Nausea, persistent vomiting, abdominal pain, and diarrhea.
- Lethargy and headache may occur but are less frequent.
- In severe poisonings, a beefy red skin rash affecting palms, soles, buttocks and scrotum has been described. With severe poisoning,
erythematous and exfoliative rash, unconsciousness, respiratory depression, and renal failure.

Source for Group Symptoms: Recognition and Management of Pesticide Poisoning, 5th edition, U.S. EPA, Chapter 8.

Treatment for Borate Poisoning
See: Recognition and Management of Pesticide Poisoning, 5th edition, U.S. EPA, Chapter 8, page 76.

https://cen.acs.org/physical-chemistry/chemical-bonding/Chemists-claim-ve-defined-first/96/i22

Chemists claim they’ve defined the first new class of stereoisomers in 50 years
Akamptisomers result from bond-angle inversion
by Sam Lemonick
MAY 24, 2018 | APPEARED IN VOLUME 96, ISSUE 22

Credit: Jeffrey Reimers
A bond-angle inversion produces akamptisomers of a porphyrin macrocycle containing a boron (pink) and oxygen (red) bridge.
For the first time in 50 years, researchers say they have identified a new category of stereoisomers (Nat. Chem. 2018, DOI: 10.1038/s41557-018-0043-6).

The new class is characterized by a bond-angle inversion in which the central atom in a bent, singly bonded trio of different atoms flexes in the opposite direction. If this trio were an independent molecule, its two different isomers would be impossible to isolate because a simple rotation of the bonds would return the molecule to its original configuration. When placed in the middle of a larger molecule, however, that rotation is blocked, and the situation changes. Peter J. Canfield, a Ph.D. student advised by Jeffrey R. Reimers of Shanghai University and the University of Technology Sydney and

uncovered this isomerism while making porphyrin macrocycles with a boron-oxygen-boron bridge.

Unable to name the four versions of the product they had made using standard nomenclature, the researchers are arguing for a new category of stereoisomer. The porphyrin ring in the team’s compounds prevents rotation around the boron-oxygen bonds, enabling isomer isolation. The researchers call these akamptisomers, after the Greek word for inflexible. They synthesized four of the eight predicted akamptisomers and enantiomers of their product. Density functional calculations suggest the other four are less stable and may be impossible to produce.

Reimers says aspects of what the team discovered were already known but argues that recognizing these isomers as a defined group will help researchers determine whether the compounds have important new properties. Several patents have been filed related to the discovery. Like other kinds of stereoisomers, akamptisomers’s ability to assume different shapes with similar chemistry could be useful in making drug molecules. They could also act as molecular switches in electronics, although Canfield notes that commercial devices are likely years away. “At this stage we only dream about practical significance, but the mathematical significance of our discovery is clear and timeless,” Reimers says.

“I can imagine potential utilities of akamptisomers,” says Steven LaPlante, a medicinal chemist at the University of Quebec National Institute of Scientific Research, confirming that they could be used to design alternative drugs or molecular switches.

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CORRECTION: This story was updated on May 25, 2018, to correct the description of the bond-angle inversion in these isomers. The inversion is not irreversible.
Chemical & Engineering News
ISSN 0009-2347
Copyright © 2018 American Chemical Society

God says he will destroy the wicked men doing this that harm children . animals, poor,meek righteous man, ungodly the bloody wicked men that lay and wait to kill off the unsuspecting , and those wicked that want to destroy God’s world