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Search references for XANTHATE. Phrases containing XANTHATE
See searches and references containing XANTHATE!XANTHATE
Salt that is a metal-thioate/O-esters of dithiocarbonate
A xanthate is a salt or ester of a xanthic acid. The formula of the salt of xanthic acid is [R−O−CS2]−M+ (where R is organyl group and M is usually Na
Xanthate
Chemical compound
Sodium ethyl xanthate (SEX) is an organosulfur compound with the chemical formula CH3CH2OCS2Na. It is a pale yellow powder, which is usually obtained as
Sodium_ethyl_xanthate
Chemical compound
Potassium amyl xanthate (/pəˈtæsiəm ˌæmɪl ˈzænθeɪt/) is an organosulfur compound with the chemical formula CH3(CH2)4OCS2K. It is a pale yellow powder with
Potassium_amyl_xanthate
Chemical compound
Potassium ethyl xanthate (KEX, or PEX) is an organosulfur compound with the chemical formula CH3CH2OCS2K. It is a pale yellow powder that is used in the
Potassium_ethyl_xanthate
Cellulose-based semi-synthetic fiber
treatment of that solution with carbon disulfide to give a xanthate derivative. The xanthate is then converted back to a cellulose fiber in a subsequent
Rayon
Process for selectively separating of hydrophobic materials from hydrophilic
xanthate salts, including potassium amyl xanthate (PAX), potassium isobutyl xanthate (PIBX), potassium ethyl xanthate (KEX), sodium isobutyl xanthate
Froth_flotation
Topics referred to by the same term
Germanic peoples Sex, abbreviation of Sextans, a constellation Sodium ethyl xanthate, a chemical compound Sex-, the Latin prefix meaning 6 Sex Peak, a mountain
Sex
Simplest secondary alcohol
Easy – A How-To Guide". FauxHammer. 7 May 2020. "Sodium Isopropyl Xanthate, SIPX, Xanthate". 3DChem.com. Archived from the original on 4 May 2012. Retrieved
Isopropyl_alcohol
Organic reaction
converted into a reactive carbonothioyl intermediate such as a thionoester or xanthate 2. Heating of AIBN results in its homolytic cleavage, generating two 2-cyanoprop-2-yl
Barton–McCombie_deoxygenation
Chemical reaction
removal of water from alcohols to produce alkenes. The intermediate is a xanthate. It is named for its discoverer, the Russian chemist Lev Chugaev, who first
Chugaev_elimination
Derivatives of the carbonate ion
Trithiocarbonic acid Xanthate Thioxanthate Sodium ethyl xanthate (SEX) Potassium ethyl xanthate (KEX) Potassium amyl xanthate Potassium trithiocarbonate
Thiocarbonate
Varieties of the color yellow
adjectival suffix -icus. The color "xanthic" is the color of Xanthine and Xanthate, both of which are xanthic acids.[citation needed] Lists of colors "CSS
Shades_of_yellow
Chemical group (–OH)
Sulfone Sulfonic acid Thioketone Thial Thioester Thionoester Thioxanthate Xanthate Boron Boronic acid Borinic acid Selenium Selenol Selenonic acid Seleninic
Hydroxy_group
Chemical reaction that produces polymers
thiocarbonylthio compounds, such as dithioesters, thiocarbamates, and xanthates, to mediate the polymerization via a reversible chain transfer process
Reversible addition−fragmentation chain-transfer polymerization
Reversible_addition−fragmentation_chain-transfer_polymerization
Artificially manufactured fibers, often based on polymers
cellulose under alkaline conditions gave a highly viscous solution of xanthate. The first commercial viscose rayon was produced by the UK company Courtaulds
Synthetic_fiber
Organic compound
Sulfone Sulfonic acid Thioketone Thial Thioester Thionoester Thioxanthate Xanthate Boron Boronic acid Borinic acid Selenium Selenol Selenonic acid Seleninic
Urea
Type of organic chemical reaction
group, a third type of reaction, E1CB, exists. Finally, the pyrolysis of xanthate and acetate esters proceed through an "internal" elimination mechanism
Elimination_reaction
Organic compounds of the form >C=O
Sulfone Sulfonic acid Thioketone Thial Thioester Thionoester Thioxanthate Xanthate Boron Boronic acid Borinic acid Selenium Selenol Selenonic acid Seleninic
Ketone
Sulfone Sulfonic acid Thioketone Thial Thioester Thionoester Thioxanthate Xanthate Boron Boronic acid Borinic acid Selenium Selenol Selenonic acid Seleninic
Reductone
Chemical compound
convenient method of controlling the synthesis of PVA by the addition of a xanthate or a dithiocarbamate chain transfer agent. Vinyl acetate is useful in organic
Vinyl_acetate
Organic compounds made of alkyl/aryl groups bound to oxygen (R–O–R')
Sulfone Sulfonic acid Thioketone Thial Thioester Thionoester Thioxanthate Xanthate Boron Boronic acid Borinic acid Selenium Selenol Selenonic acid Seleninic
Ether
Textile made from various parts of the bamboo plant
the fibers with lye, and adds carbon disulfide to form sodium cellulose xanthate. After time, temperature, and various inorganic and organic additives (including
Bamboo_textile
Chemical group (–CH2–CH3)
Sulfone Sulfonic acid Thioketone Thial Thioester Thionoester Thioxanthate Xanthate Boron Boronic acid Borinic acid Selenium Selenol Selenonic acid Seleninic
Ethyl_group
Type of organosulfur compound
Sulfone Sulfonic acid Thioketone Thial Thioester Thionoester Thioxanthate Xanthate Boron Boronic acid Borinic acid Selenium Selenol Selenonic acid Seleninic
Sulfinylamine
Compound derived from an acid
Sulfone Sulfonic acid Thioketone Thial Thioester Thionoester Thioxanthate Xanthate Boron Boronic acid Borinic acid Selenium Selenol Selenonic acid Seleninic
Ester
Organic molecule with two different functional groups
Sulfone Sulfonic acid Thioketone Thial Thioester Thionoester Thioxanthate Xanthate Boron Boronic acid Borinic acid Selenium Selenol Selenonic acid Seleninic
Bifunctionality
Topics referred to by the same term
in medicine Plasma exchange, a form of plasmapheresis Potassium ethyl xanthate, an organosulfur ligand used as a flotation agent in the mining industry
PEX_(disambiguation)
Class of chemical compounds
Sulfone Sulfonic acid Thioketone Thial Thioester Thionoester Thioxanthate Xanthate Boron Boronic acid Borinic acid Selenium Selenol Selenonic acid Seleninic
Imide
Organosulfur compounds of the form R–SC(=O)–R′
existing methyl thionoester with an alcohol under base-catalyzed conditions. Xanthates and thioamides can be transformed to thionoesters under metal-catalyzed
Thioester
Functional group (C=O)
Sulfone Sulfonic acid Thioketone Thial Thioester Thionoester Thioxanthate Xanthate Boron Boronic acid Borinic acid Selenium Selenol Selenonic acid Seleninic
Carbonyl_group
Organic compound containing the functional group R–CH=O
Sulfone Sulfonic acid Thioketone Thial Thioester Thionoester Thioxanthate Xanthate Boron Boronic acid Borinic acid Selenium Selenol Selenonic acid Seleninic
Aldehyde
Sulfone Sulfonic acid Thioketone Thial Thioester Thionoester Thioxanthate Xanthate Boron Boronic acid Borinic acid Selenium Selenol Selenonic acid Seleninic
Arsonic acid (functional group)
Arsonic_acid_(functional_group)
Class of chemical compounds
Sulfone Sulfonic acid Thioketone Thial Thioester Thionoester Thioxanthate Xanthate Boron Boronic acid Borinic acid Selenium Selenol Selenonic acid Seleninic
Hydroperoxide
Organic compound with at least one hydroxyl (–OH) group
ethylene: A more controlled elimination reaction requires the formation of the xanthate ester. Tertiary alcohols react with strong acids to generate carbocations
Alcohol_(chemistry)
Hydrocarbon compound containing one or more C=C bonds
H2O An alcohol may also be converted to a better leaving group (e.g., xanthate), so as to allow a milder syn-elimination such as the Chugaev elimination
Alkene
Chemical reaction which transfers an alkyl group between molecules
Sulfone Sulfonic acid Thioketone Thial Thioester Thionoester Thioxanthate Xanthate Boron Boronic acid Borinic acid Selenium Selenol Selenonic acid Seleninic
Transalkylation
Class of organic compounds
Sulfone Sulfonic acid Thioketone Thial Thioester Thionoester Thioxanthate Xanthate Boron Boronic acid Borinic acid Selenium Selenol Selenonic acid Seleninic
Chlorofluorocarbon
Reaction mechanism in organic chemistry
The Chugaev elimination is the pyrolysis of a xanthate ester, resulting in an olefin. To form the xanthate ester, an alcohol reacts with carbon disulfide
Ei_mechanism
Chemical compound
In the viscose process, cellulose is made soluble by conversion to its xanthate derivatives. With NMMO, cellulose is not derivatized but dissolves to give
N-Methylmorpholine_N-oxide
Chemical compounds with the structure R–O–O–R'
Sulfone Sulfonic acid Thioketone Thial Thioester Thionoester Thioxanthate Xanthate Boron Boronic acid Borinic acid Selenium Selenol Selenonic acid Seleninic
Peroxide
Chemical compound with the group –N+≡C–
Sulfone Sulfonic acid Thioketone Thial Thioester Thionoester Thioxanthate Xanthate Boron Boronic acid Borinic acid Selenium Selenol Selenonic acid Seleninic
Isocyanide
Chemical compounds and groups containing nitrogen with a lone pair (:N)
Sulfone Sulfonic acid Thioketone Thial Thioester Thionoester Thioxanthate Xanthate Boron Boronic acid Borinic acid Selenium Selenol Selenonic acid Seleninic
Amine
Free radical
Sulfone Sulfonic acid Thioketone Thial Thioester Thionoester Thioxanthate Xanthate Boron Boronic acid Borinic acid Selenium Selenol Selenonic acid Seleninic
Propenyl_group
Organic compound containing a –C(=O)OH group
Sulfone Sulfonic acid Thioketone Thial Thioester Thionoester Thioxanthate Xanthate Boron Boronic acid Borinic acid Selenium Selenol Selenonic acid Seleninic
Carboxylic_acid
Organosulfur compound of the form >S(=O)2
Sulfone Sulfonic acid Thioketone Thial Thioester Thionoester Thioxanthate Xanthate Boron Boronic acid Borinic acid Selenium Selenol Selenonic acid Seleninic
Sulfone
Any organic compound having a sulfanyl group (–SH)
Sulfone Sulfonic acid Thioketone Thial Thioester Thionoester Thioxanthate Xanthate Boron Boronic acid Borinic acid Selenium Selenol Selenonic acid Seleninic
Thiol
Chemical compound
acid is obtained by the action of dilute sulfuric acid on potassium ethyl xanthate at 0 °C. Ethyl xanthic acid is a colorless, labile oil. In aqueous solution
Ethyl_xanthic_acid
Functional group consisting of sulfur double-bonded to oxygen
Sulfone Sulfonic acid Thioketone Thial Thioester Thionoester Thioxanthate Xanthate Boron Boronic acid Borinic acid Selenium Selenol Selenonic acid Seleninic
Thionyl_group
Cyclic chemical group (–C6H5)
Sulfone Sulfonic acid Thioketone Thial Thioester Thionoester Thioxanthate Xanthate Boron Boronic acid Borinic acid Selenium Selenol Selenonic acid Seleninic
Phenyl_group
Chemical group (>N–C(=O)–O–)
Sulfone Sulfonic acid Thioketone Thial Thioester Thionoester Thioxanthate Xanthate Boron Boronic acid Borinic acid Selenium Selenol Selenonic acid Seleninic
Carbamate
Organic compound containing an –NO2 group
Sulfone Sulfonic acid Thioketone Thial Thioester Thionoester Thioxanthate Xanthate Boron Boronic acid Borinic acid Selenium Selenol Selenonic acid Seleninic
Nitro_compound
Organic molecule containing a neutral carbon with two unbound valence electrons
Sulfone Sulfonic acid Thioketone Thial Thioester Thionoester Thioxanthate Xanthate Boron Boronic acid Borinic acid Selenium Selenol Selenonic acid Seleninic
Carbene
Organic compounds of the form RC(=O)NR′R″
Sulfone Sulfonic acid Thioketone Thial Thioester Thionoester Thioxanthate Xanthate Boron Boronic acid Borinic acid Selenium Selenol Selenonic acid Seleninic
Amide
Anion with formula OCN and charge –1
Sulfone Sulfonic acid Thioketone Thial Thioester Thionoester Thioxanthate Xanthate Boron Boronic acid Borinic acid Selenium Selenol Selenonic acid Seleninic
Cyanate
Chemical group (>S(=O)2)
Sulfone Sulfonic acid Thioketone Thial Thioester Thionoester Thioxanthate Xanthate Boron Boronic acid Borinic acid Selenium Selenol Selenonic acid Seleninic
Sulfonyl_group
Chemical compound
example, amines afford dithiocarbamates: 2 R2NH + CS2 → [R2NH2+][R2NCS2−] Xanthates form similarly from alkoxides: RONa + CS2 → [Na+][ROCS2−] This reaction
Carbon_disulfide
Functional group with the chemical structure R–S–S–R′
Sulfone Sulfonic acid Thioketone Thial Thioester Thionoester Thioxanthate Xanthate Boron Boronic acid Borinic acid Selenium Selenol Selenonic acid Seleninic
Disulfide
Chemical compound
commonly used as antioxidants in rubber production, obtained by condensing xanthate esters. Condensation of substituted o-phenylenediamine with diketones yields
O-Phenylenediamine
Organic compound with the structure >C(O–)2
Sulfone Sulfonic acid Thioketone Thial Thioester Thionoester Thioxanthate Xanthate Boron Boronic acid Borinic acid Selenium Selenol Selenonic acid Seleninic
Acetal
Halogen compounds derived from methane
Sulfone Sulfonic acid Thioketone Thial Thioester Thionoester Thioxanthate Xanthate Boron Boronic acid Borinic acid Selenium Selenol Selenonic acid Seleninic
Halomethane
Species of plant
singular, or two to four, ascending from the leaf axils. Six thick, creamy or xanthate petals display in double whorls, and green on the outside, but either creamy
Annona_senegalensis
Organosulfur compound of the form R–SOH
Sulfone Sulfonic acid Thioketone Thial Thioester Thionoester Thioxanthate Xanthate Boron Boronic acid Borinic acid Selenium Selenol Selenonic acid Seleninic
Sulfenic_acid
Group of atoms giving a molecule characteristic properties
Sulfone Sulfonic acid Thioketone Thial Thioester Thionoester Thioxanthate Xanthate Boron Boronic acid Borinic acid Selenium Selenol Selenonic acid Seleninic
Functional_group
Polyatomic ion (NO3, charge –1) found in explosives and fertilisers
Sulfone Sulfonic acid Thioketone Thial Thioester Thionoester Thioxanthate Xanthate Boron Boronic acid Borinic acid Selenium Selenol Selenonic acid Seleninic
Nitrate
Hydrocarbon compound (C6H6)
Sulfone Sulfonic acid Thioketone Thial Thioester Thionoester Thioxanthate Xanthate Boron Boronic acid Borinic acid Selenium Selenol Selenonic acid Seleninic
Benzene
Organic compound or functional group containing a C=N bond
Sulfone Sulfonic acid Thioketone Thial Thioester Thionoester Thioxanthate Xanthate Boron Boronic acid Borinic acid Selenium Selenol Selenonic acid Seleninic
Imine
Chemical group (R–O)
Sulfone Sulfonic acid Thioketone Thial Thioester Thionoester Thioxanthate Xanthate Boron Boronic acid Borinic acid Selenium Selenol Selenonic acid Seleninic
Alkoxy_group
Chemical group (–N=C=O)
Sulfone Sulfonic acid Thioketone Thial Thioester Thionoester Thioxanthate Xanthate Boron Boronic acid Borinic acid Selenium Selenol Selenonic acid Seleninic
Isocyanate
Chemical group derived from alkanes (one hydrogen removed)
Sulfone Sulfonic acid Thioketone Thial Thioester Thionoester Thioxanthate Xanthate Boron Boronic acid Borinic acid Selenium Selenol Selenonic acid Seleninic
Alkyl_group
Chemical compound
starting material is an aniline through the diazonium salt (ArN2X) and the xanthate (ArS(C=S)OR). Alternatively, sodium sulfide and triazenes can react in
Thiophenol
Danish organic chemist (1789–1847)
performed pioneering studies in organosulfur chemistry, discovering the xanthates in 1823. William Christopher Zeise was born 15 October 1789 in Slagelse
William_Christopher_Zeise
Hydrocarbon compound (H2C=CH2)
Sulfone Sulfonic acid Thioketone Thial Thioester Thionoester Thioxanthate Xanthate Boron Boronic acid Borinic acid Selenium Selenol Selenonic acid Seleninic
Ethylene
Organic compounds with a carbon-carbon-oxygen ring
Sulfone Sulfonic acid Thioketone Thial Thioester Thionoester Thioxanthate Xanthate Boron Boronic acid Borinic acid Selenium Selenol Selenonic acid Seleninic
Epoxide
List of chemical classification and labeling systems
Sulfone Sulfonic acid Thioketone Thial Thioester Thionoester Thioxanthate Xanthate Boron Boronic acid Borinic acid Selenium Selenol Selenonic acid Seleninic
List of chemical classifications
List_of_chemical_classifications
Class of chemical compounds
Sulfone Sulfonic acid Thioketone Thial Thioester Thionoester Thioxanthate Xanthate Boron Boronic acid Borinic acid Selenium Selenol Selenonic acid Seleninic
Sulfinic_acid
Sulfone Sulfonic acid Thioketone Thial Thioester Thionoester Thioxanthate Xanthate Boron Boronic acid Borinic acid Selenium Selenol Selenonic acid Seleninic
Organic_selenocyanates
Class of organic compounds
Sulfone Sulfonic acid Thioketone Thial Thioester Thionoester Thioxanthate Xanthate Boron Boronic acid Borinic acid Selenium Selenol Selenonic acid Seleninic
Hydrazone
Class of chemical compounds
Sulfone Sulfonic acid Thioketone Thial Thioester Thionoester Thioxanthate Xanthate Boron Boronic acid Borinic acid Selenium Selenol Selenonic acid Seleninic
Thiosulfonate
Chemical group (–CH3) derived from methane
Sulfone Sulfonic acid Thioketone Thial Thioester Thionoester Thioxanthate Xanthate Boron Boronic acid Borinic acid Selenium Selenol Selenonic acid Seleninic
Methyl_group
Chemical group, –C(=O)CH3
Sulfone Sulfonic acid Thioketone Thial Thioester Thionoester Thioxanthate Xanthate Boron Boronic acid Borinic acid Selenium Selenol Selenonic acid Seleninic
Acetyl_group
Chemical group (–C(=O)C6H5
Sulfone Sulfonic acid Thioketone Thial Thioester Thionoester Thioxanthate Xanthate Boron Boronic acid Borinic acid Selenium Selenol Selenonic acid Seleninic
Benzoyl_group
Process to transform the material properties of natural rubber
in compounds with fewer curing site such as EPDM. Xanthates (principally, zinc isopropyl xanthate) are important in the vulcanization of latex, which
Sulfur_vulcanization
Organic compounds with a diazenyl group (–N=N–)
Sulfone Sulfonic acid Thioketone Thial Thioester Thionoester Thioxanthate Xanthate Boron Boronic acid Borinic acid Selenium Selenol Selenonic acid Seleninic
Azo_compound
Organic compounds of the form R–O–O–R′
Sulfone Sulfonic acid Thioketone Thial Thioester Thionoester Thioxanthate Xanthate Boron Boronic acid Borinic acid Selenium Selenol Selenonic acid Seleninic
Organic_peroxides
Chemical group (–C4H9) derived from butane
Sulfone Sulfonic acid Thioketone Thial Thioester Thionoester Thioxanthate Xanthate Boron Boronic acid Borinic acid Selenium Selenol Selenonic acid Seleninic
Butyl_group
Sulfone Sulfonic acid Thioketone Thial Thioester Thionoester Thioxanthate Xanthate Boron Boronic acid Borinic acid Selenium Selenol Selenonic acid Seleninic
Organic_thiocyanates
Organic compound containing C–PO(OR)2 groups
Sulfone Sulfonic acid Thioketone Thial Thioester Thionoester Thioxanthate Xanthate Boron Boronic acid Borinic acid Selenium Selenol Selenonic acid Seleninic
Phosphonate
Bleached wood pulp or cotton linters with a high cellulose content
regenerated cellulose process the cellulose is converted to cellulose xanthate which dissolves easily in caustic soda. The resulting viscous liquid can
Dissolving_pulp
Organic compounds with the formula P(OR)2R
Sulfone Sulfonic acid Thioketone Thial Thioester Thionoester Thioxanthate Xanthate Boron Boronic acid Borinic acid Selenium Selenol Selenonic acid Seleninic
Phosphonite
Fjord in western Norway
including 2 tonnes (2.0 long tons; 2.2 short tons) of SIBX (sodium isobutyl xanthate). As of January 2024[update], after a 15-year dispute, Nordic Mining has
Førde_Fjord
Organic compounds with the structure R–S(=O)2–OH
Sulfone Sulfonic acid Thioketone Thial Thioester Thionoester Thioxanthate Xanthate Boron Boronic acid Borinic acid Selenium Selenol Selenonic acid Seleninic
Sulfonic_acid
Group of chemical compounds derived from alkanes containing one or more halogens
Sulfone Sulfonic acid Thioketone Thial Thioester Thionoester Thioxanthate Xanthate Boron Boronic acid Borinic acid Selenium Selenol Selenonic acid Seleninic
Haloalkane
(ROC(S)S)2. Usually yellow solids, they are the product of the oxidation of xanthate salts. A common derivative is diethyl dixanthogen disulfide. Diisopropyl
Dixanthogen_disulfide
Organic compound with a –C≡N functional group
Sulfone Sulfonic acid Thioketone Thial Thioester Thionoester Thioxanthate Xanthate Boron Boronic acid Borinic acid Selenium Selenol Selenonic acid Seleninic
Nitrile
Functional group
Sulfone Sulfonic acid Thioketone Thial Thioester Thionoester Thioxanthate Xanthate Boron Boronic acid Borinic acid Selenium Selenol Selenonic acid Seleninic
Methylenedioxy
Nitrogen-based molecule
Sulfone Sulfonic acid Thioketone Thial Thioester Thionoester Thioxanthate Xanthate Boron Boronic acid Borinic acid Selenium Selenol Selenonic acid Seleninic
Nitrene
Chemical group (–CH=CH2)
Sulfone Sulfonic acid Thioketone Thial Thioester Thionoester Thioxanthate Xanthate Boron Boronic acid Borinic acid Selenium Selenol Selenonic acid Seleninic
Vinyl_group
Chemical group (R–C=O)
Sulfone Sulfonic acid Thioketone Thial Thioester Thionoester Thioxanthate Xanthate Boron Boronic acid Borinic acid Selenium Selenol Selenonic acid Seleninic
Acyl_group
Chemical group (–N=C=S)
Sulfone Sulfonic acid Thioketone Thial Thioester Thionoester Thioxanthate Xanthate Boron Boronic acid Borinic acid Selenium Selenol Selenonic acid Seleninic
Isothiocyanate
Chemical group (>N–C(=S)–S–)
basic than structurally related anions such as dithiocarboxylates and xanthates. Consequently, they tend to bind as bidentate ligands. Another consequence
Dithiocarbamate
XANTHATE
XANTHATE
XANTHATE
XANTHATE
Male
Hebrew
(×™ï‹×ֵל) Hebrew name YOWEL means "Jehovah is God" or "to whom Jehovah is God." In the bible, this is the name of many characters, including one of the minor prophets. Joel is the Anglicized form.Â
Boy/Male
German, Hebrew
Bear
Boy/Male
Bengali, Gujarati, Hindu, Indian, Kannada, Malayalam, Marathi
Sky
Boy/Male
Arabic Muslim
Sparkling.
Girl/Female
Hindu
From a Arabian descent and means jewel
Boy/Male
Indian, Punjabi, Sikh
One who Reflects the Ultimate Truth
Girl/Female
Tamil
Shrigeeta | à®·à¯à®°à¯€à®•à¯€à®¤à®¾
The sacred Geeta
Girl/Female
Greek
People's victory.
Girl/Female
American, British, English, French, Latin
To Open; April Month; Opening Buds of Spring; French Version of April; The Month Name; Opening Up
Surname or Lastname
English, French, German, Czech, Slovak, Polish, Ukrainian, Belorussian, Hungarian (Urbán), and Jewish (eastern Ashkenazic)
English, French, German, Czech, Slovak, Polish, Ukrainian, Belorussian, Hungarian (Urbán), and Jewish (eastern Ashkenazic) : from a medieval personal name (Latin Urbanus meaning ‘city dweller’, a derivative of urbs ‘town’, ‘city’). The name was borne by a 4th-century saint, the patron saint of vines, and by seven early popes. The Jewish surname represents an adoption of the Polish personal name.
XANTHATE
XANTHATE
XANTHATE
XANTHATE
XANTHATE
n.
A salt of xanthic; a xanthogenate.
n.
One of the gaseous or volatile decomposition products of the xanthates, and probably identical with carbon disulphide.