Explore: Health Aspects Of Methyl Ether
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Books Results
Source: The Open Library
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Search results from The Open Library
1Research study on BIS(chloromethyl)ether formation and detection in selected work environments
By C. C. Yao
“Research study on BIS(chloromethyl)ether formation and detection in selected work environments” Metadata:
- Title: ➤ Research study on BIS(chloromethyl)ether formation and detection in selected work environments
- Author: C. C. Yao
- Language: English
- Number of Pages: Median: 151
- Publisher: ➤ U.S. Dept. of Health, Education, and Welfare, Public Health Service, Center for Disease Control, National Institute for Occupational Safety and Health, Division of Surveillance, Hazard Evaluations, and Field Studies
- Publish Date: 1979
- Publish Location: Cincinnati
“Research study on BIS(chloromethyl)ether formation and detection in selected work environments” Subjects and Themes:
- Subjects: ➤ Chlorides - Chloromethyl group - Chloromethyl methyl ether - Environmental monitoring - Ether - Formaldehyde - Health aspects - Health aspects of Chloromethyl group - Health aspects of Chloromethyl methyl ether - Health aspects of Methyl ether - Industrial hygiene - Methyl ether - Toxicology - Safety measures
Edition Identifiers:
- The Open Library ID: OL17720590M - OL17818931M
- Online Computer Library Center (OCLC) ID: 4841051
Access and General Info:
- First Year Published: 1979
- Is Full Text Available: No
- Is The Book Public: No
- Access Status: No_ebook
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Wiki
Source: Wikipedia
Wikipedia Results
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Methyl isocyanate
Methyl isocyanate (MIC) is an organic compound with the molecular formula CH3NCO. Synonyms are isocyanatomethane and methyl carbylamine. Methyl isocyanate
Diazomethane
needed as a solution in ether and used as such. It converts carboxylic acids to methyl esters and phenols into their methyl ethers. The reaction is thought
Furan
temperature. It is soluble in common organic solvents, including alcohol, ether, and acetone, and is slightly soluble in water. Its odor is "strong, ethereal;
Xylometazoline
solution). 5-tert-Butyl-m-xylene is reacted with chloromethyl methyl ether in the presence of zinc chloride to form 2,6-dimethyl-4-tert-butyl-benzylchloride
Ethyl oleate
pheromone in honeybees. By the process of ethenolysis, the methyl ester of oleic acid, converts to 1-decene and methyl 9-decenoate: CH3(CH2)7CH=CH(CH2)7CO2Me
Quinestrol
(17α-ethynylestradiol). Closely related estrogens include mestranol (ethinylestradiol 3-methyl ether) and ethinylestradiol sulfonate (EES; Turisteron; ethinylestradiol
Mestranol
the initial chemical syntheses of noretynodrel had been contaminated with small amounts (1–2%) of the 3-methyl ether of ethinylestradiol (noretynodrel
NMDA receptor
The N-methyl-D-aspartate receptor (also known as the NMDA receptor or NMDAR), is a glutamate receptor and predominantly Ca2+ ion channel found in neurons
Organolithium reagent
tetramer in the crystallized ether solvate, and as a mixture of dimer and tetramer in ether solution. As the structures of organolithium reagents change
Mesterolone
1α-methyl-4,5α-dihydrotestosterone (1α-methyl-DHT) or as 1α-methyl-5α-androstan-17β-ol-3-one, is a synthetic androstane steroid and derivative of DHT