calcium carbide
Conditions | Yield |
---|---|
With biochars (apricot shell, willow or pine wood etc.) In neat (no solvent) Kinetics; reaction at 1650-1750 °C; detd. by XRD; | 97% |
With sugar coal In neat (no solvent) heating CaO with sugar coal (1:3) at 1700°C, pressure about 100 Torr, during less 1 hour;; about 97% CaC2;; | |
With pyrographite In neat (no solvent) Electric Arc; from mixture of CaO and char coal powder; carbon electrodes, 12-14 A, 10-15 min; special app. described;; |
Conditions | Yield |
---|---|
In further solvent(s) acetylene carbon black reacted with CaCH2 in Ca/Li flux; sealed ampules heated to 1323 K in 2 h and kept at this temp. for 2 h; cooled to 1073 K in 24 h, cooled to 773 K in 108 h, centrifuged; elem. anal.; | A 70% B n/a |
calcium carbide
Conditions | Yield |
---|---|
With sodium In neat (no solvent) mixture of CaCl2, retort carbon and metallic Na in Fe crucible; 0.5 h at light red heat;; | 50% |
With retort carbon; Na In neat (no solvent) mixture of CaCl2, retort carbon and metallic Na in Fe crucible; 0.5 h at light red heat;; | 50% |
Conditions | Yield |
---|---|
With calcium sulfate at 1130 - 1250℃; im Vakuum; isomer(ic) II; | |
at 1100 - 1150℃; isomer(ic) III; | |
at 1130℃; zuletzt bei 1250-1300grad; isomer(ic) IV; |
calcium carbide
Conditions | Yield |
---|---|
isomer(ic) IV; |
calcium carbide
Conditions | Yield |
---|---|
With hydrogen; calcium at 1150 - 1250℃; | |
With argon; calcium at 1150 - 1250℃; |
Conditions | Yield |
---|---|
isomer(ic) II; |
Conditions | Yield |
---|---|
With nitrogen at 1050 - 1300℃; isomer(ic) II; | |
at 1050 - 1300℃; isomer(ic) III; |
Conditions | Yield |
---|---|
With calcium sulfate at 1700℃; im Hochvakuum; isomer(ic) II; | |
at 1700℃; im Hochvakuum, dann in Stickstoff-Atmosphaere unter 30-120 mm bei 1250grad; isomer(ic) III; | |
at 1700℃; im Hochvakuum; isomer(ic) IV; | |
im elektrischen Ofen; isomer(ic) IV; |
Conditions | Yield |
---|---|
In neat (no solvent) byproducts: Ca-silicide; at 1690-1740°C;; | |
In neat (no solvent) byproducts: Ca-silicide; at 1690-1740°C;; | |
In neat (no solvent) |
Conditions | Yield |
---|---|
at >845°C; | |
at >845°C; |
Conditions | Yield |
---|---|
With carbon dioxide | |
With CO2 by fast heating; | |
With CO2 |
Conditions | Yield |
---|---|
With CO2 by slow heating; |
Conditions | Yield |
---|---|
With tetrachloromethane burning in the presence of silica gel with excess of Ca after ignition with a mixture of CaSi2+KNO3; | |
With CCl4 burning in the presence of silica gel with excess of Ca after ignition with a mixture of CaSi2+KNO3; |
Conditions | Yield |
---|---|
With soot at red heat; | |
In neat (no solvent) liquid, heated Ca was treated with organic compounds;; | |
With char coal In neat (no solvent) burning heated pieces of Ca on char coal;; |
Conditions | Yield |
---|---|
With CO at read heat; | |
With methane over dark red heat; |
Conditions | Yield |
---|---|
at dark red heat; |
potassium thioacyanate
calcium
C
calcium carbide
D
pyrographite
Conditions | Yield |
---|---|
at 300-400°C and 25 Torr with 50% conversion of Ca; | |
at 300-400°C and 25 Torr with 50% conversion of Ca; |
Conditions | Yield |
---|---|
over dark red heat; |
Conditions | Yield |
---|---|
explosion after ignition with Mg; | |
explosion after ignition with Mg; |
Conditions | Yield |
---|---|
over red heat; | |
In neat (no solvent) 1.5 h heating in closed Fe crucible at 1150-1200°C;; 94% CaC2, 2% free carbon, small amts. of CaO and up to 2% impurities;; | |
In neat (no solvent) C (calcinated soot or calcinated, powdered petroleum coke); Fe crucible in resistance furnace under Ar: 825 Torr, 10-30 min, 1250°C and 3-6 Torr, 15 min, 1150°C; keep under N2 and P2O5 in desiccator;; melting at 2200°C, 750 Torr under Ar; product contains 90-93% CaC2, 2-4% graphite, up to 3% CaO and about 2% Fe and Al;; |
calcium carbide
Conditions | Yield |
---|---|
With hydrogen In neat (no solvent) use of carbon and CaO from lime through reduction with H2;; | |
With aluminium In neat (no solvent) Electric Arc; under exclusion of air;; | |
With Sucrose In neat (no solvent) calcination;; |
Conditions | Yield |
---|---|
In neat (no solvent) byproducts: CaO, CO, CO2; Electric Arc; under heating, molar ratio carbonate:carbon=1:0.3, under Ar; | |
In neat (no solvent) description of dust control;; | |
With aluminum oxide In neat (no solvent) byproducts: Al; conducting the process; modification of pederson process: CaC2 as intermediate;; |
ethene
calcium
A
calcium hydride
B
calcium carbide
C
pyrographite
Conditions | Yield |
---|---|
In neat (no solvent) dark red heat; crust of CaC2, C and CaH2 inhibit reaction;; | |
In neat (no solvent) dark red heat; crust of CaC2, C and CaH2 inhibit reaction;; |
Conditions | Yield |
---|---|
In neat (no solvent) at very high temp.;; |
Conditions | Yield |
---|---|
In neat (no solvent) carbon forms in an electric furnace CaC2;; |
Conditions | Yield |
---|---|
In neat (no solvent) enthalpy of reaction given;; |
Conditions | Yield |
---|---|
In neat (no solvent) heating with methane;; |
Conditions | Yield |
---|---|
In neat (no solvent) in electrical furnace at 500 - 1500°C;; | |
With carbon dioxide; carbon monoxide; nitrogen In neat (no solvent) byproducts: NO; reaction with CO2 from lime;; | |
With silica gel; iron In neat (no solvent) byproducts: FeSi; |
Conditions | Yield |
---|---|
With water Hydrolysis; | 100% |
With water In water decompn.;; | |
With hydrogen In neat (no solvent) byproducts: Ca; at 2275°C pressure of H2 1 atm;; |
4-hydroxybenzaldehyde 4-methylbenzenesulfonate ester
calcium carbide
4,4'-(ethyne-1,2-diyl)bis(4,1-phenylene) bis(4-methylbenzenesulfonate)
Conditions | Yield |
---|---|
With copper(l) iodide; palladium diacetate; triethylamine; triphenylphosphine In acetonitrile at 20℃; Sonogashira coupling; Inert atmosphere; | 99.4% |
Conditions | Yield |
---|---|
With copper(l) iodide; palladium diacetate; triethylamine; triphenylphosphine In acetonitrile at 20℃; Sonogashira coupling; Inert atmosphere; | 99% |
With copper(l) iodide; palladium diacetate; triethylamine; triphenylphosphine In acetonitrile at 20℃; Inert atmosphere; |
4-Iodoacetophenone
calcium carbide
1,1'-[ethyne-1,2-diylbis(4,1-phenylene)]diethanone
Conditions | Yield |
---|---|
With copper(l) iodide; palladium diacetate; triethylamine; triphenylphosphine In acetonitrile at 20℃; Sonogashira coupling; Inert atmosphere; | 99% |
Conditions | Yield |
---|---|
With copper(l) iodide; palladium diacetate; triethylamine; triphenylphosphine In acetonitrile at 20℃; Sonogashira coupling; Inert atmosphere; | 99% |
With copper(l) iodide; tetrakis(triphenylphosphine) palladium(0); water; triethylamine In N,N-dimethyl-formamide at 60℃; for 24h; |
Conditions | Yield |
---|---|
With copper(l) iodide; palladium diacetate; triethylamine; triphenylphosphine In acetonitrile at 20℃; Sonogashira coupling; Inert atmosphere; | 99% |
With copper(l) iodide; tetrakis(triphenylphosphine) palladium(0); water; triethylamine In tetrahydrofuran at 55℃; for 20h; Sonogashira Cross-Coupling; | 95% |
With copper(l) iodide; tetrakis(triphenylphosphine) palladium(0); water; triethylamine In N,N-dimethyl-formamide at 60℃; for 24h; | |
With copper(l) iodide; palladium diacetate; triethylamine; triphenylphosphine In acetonitrile at 20℃; Inert atmosphere; |
1-iodo-4-(methoxymethyl)benzene
calcium carbide
Conditions | Yield |
---|---|
With copper(l) iodide; palladium diacetate; triethylamine; triphenylphosphine In acetonitrile at 20℃; Sonogashira coupling; Inert atmosphere; | 99% |
calcium carbide
N-2-methylphenyl-3-phenylcarbohydrazonoyl chloride
Conditions | Yield |
---|---|
With triethylamine In chloroform; water at 20℃; for 48h; Sealed tube; | 99% |
Conditions | Yield |
---|---|
With triethylamine In chloroform; water at 20℃; for 48h; Sealed tube; | 99% |
calcium carbide
3-(4-(tert-butyl)phenyl)-1-phenyl-1H-pyrazole
Conditions | Yield |
---|---|
With triethylamine In chloroform; water at 20℃; for 48h; Solvent; Sealed tube; | 99% |
calcium carbide
Conditions | Yield |
---|---|
With triethylamine In chloroform-d1; water-d2 at 20℃; for 48h; Sealed tube; | 99% |
calcium carbide
Conditions | Yield |
---|---|
With triethylamine In chloroform; water at 20℃; for 48h; Sealed tube; | 99% |
calcium carbide
3,5-dimethyl-N-phenylbenzohydrazonoyl chloride
Conditions | Yield |
---|---|
With triethylamine In chloroform; water at 20℃; for 48h; Sealed tube; | 99% |
calcium carbide
4-methoxy-N'-phenylbenzohydrazonoyl chloride
3-(4-methoxy-phenyl)-1-phenyl-1H-pyrazole
Conditions | Yield |
---|---|
With triethylamine In chloroform; water at 20℃; for 48h; Sealed tube; | 99% |
calcium carbide
4-methoxy-N'-phenylbenzohydrazonoyl chloride
Conditions | Yield |
---|---|
With triethylamine In chloroform-d1; water-d2 at 20℃; for 48h; Sealed tube; | 99% |
calcium carbide
p-toluoyl chloride phenylhydrazone
3-(4-methylphenyl)-1-phenyl-1H-pyrazole
Conditions | Yield |
---|---|
With triethylamine In chloroform; water at 20℃; for 48h; Sealed tube; | 99% |
calcium carbide
3-methyl-N'-phenylbenzohydrazonoyl chloride
1-phenyl-3-(3-tolyl)-1H-pyrazole
Conditions | Yield |
---|---|
With triethylamine In chloroform; water at 20℃; for 48h; Sealed tube; | 99% |
calcium carbide
3-methyl-N'-phenylbenzohydrazonoyl chloride
Conditions | Yield |
---|---|
With triethylamine In chloroform-d1; water-d2 at 20℃; for 48h; Sealed tube; | 99% |
calcium carbide
N-phenylbenzohydrazonoyl chloride
1,3-diphenyl-1H-pyrazole
Conditions | Yield |
---|---|
With triethylamine In chloroform; water at 20℃; for 48h; Sealed tube; | 99% |
calcium carbide
N-phenylbenzohydrazonoyl chloride
Conditions | Yield |
---|---|
With triethylamine In chloroform-d1; water-d2 at 20℃; for 48h; Sealed tube; | 99% |
calcium carbide
4-bromo-N-phenylbenzohydrazonoyl chloride
3-(4-bromophenyl)-1-phenyl-1H-pyrazole
Conditions | Yield |
---|---|
With triethylamine In chloroform; water at 20℃; for 48h; Sealed tube; | 99% |
calcium carbide
4-bromo-N-phenylbenzohydrazonoyl chloride
Conditions | Yield |
---|---|
With triethylamine In chloroform-d1; water-d2 at 20℃; for 48h; Sealed tube; | 99% |
calcium carbide
N-phenyl-p-chlorobenzohydrazonoyl chloride
3-(4-chlorophenyl)-1-phenyl-1H-pyrazole
Conditions | Yield |
---|---|
With triethylamine In chloroform; water at 20℃; for 48h; Sealed tube; | 99% |
calcium carbide
chloro(phenyl)methanone p-bromophenylhydrazone
Conditions | Yield |
---|---|
With triethylamine In chloroform; water at 20℃; for 48h; Sealed tube; | 99% |
calcium carbide
chloro(phenyl)methanone p-bromophenylhydrazone
Conditions | Yield |
---|---|
With triethylamine In chloroform-d1; water-d2 at 20℃; for 48h; Sealed tube; | 99% |
calcium carbide
3,4-dichloro-N-phenylbenzohydrazonoyl chloride
Conditions | Yield |
---|---|
With triethylamine In chloroform; water at 20℃; for 48h; Sealed tube; | 99% |
calcium carbide
N-(α-chlorobenzylidene)-N'-p-chlorophenylhydrazine
1-(4-chlorophenyl)-3-phenyl-1H-pyrazole
Conditions | Yield |
---|---|
With triethylamine In chloroform; water at 20℃; for 48h; Sealed tube; | 99% |
N-phenyl-2-fluorobenzenecarbohydrazonoyl chloride
calcium carbide
Conditions | Yield |
---|---|
With triethylamine In chloroform; water at 20℃; for 48h; Sealed tube; | 99% |
N-phenyl-2-fluorobenzenecarbohydrazonoyl chloride
calcium carbide
Conditions | Yield |
---|---|
With triethylamine In chloroform-d1; water-d2 at 20℃; for 48h; Sealed tube; | 99% |
calcium carbide
Conditions | Yield |
---|---|
With triethylamine In chloroform; water at 20℃; for 48h; Sealed tube; | 99% |
The systematic name of Calcium carbide is calcium ethynediide. With the CAS registry number 75-20-7, it is also named as Acetylenogen. The product's categories are Inorganics; Carbides; Ceramics; Metal and Ceramic Science, and the other registry numbers are 12192-35-7; 195068-68-9; 261780-86-3; 761337-30-8. Besides, it is grey or black solid with a garlic-like odour, which should be sealed in dry, cool, ventilated warehouse. It is incompatible with moisture, water, strong oxidizing agents, alcohols, hydrogen chloride, magnesium. And it reacts violently with water with liberating highly flammable gas, so please keep container dry. In addition, its molecular formula is CaC2 and molecular weight is 64.10.
The other characteristics of this product can be summarized as: (1)EINECS: 200-848-3; (2)ACD/LogP: 0.37; (3)# of Rule of 5 Violations: 0; (4)ACD/LogD (pH 5.5): 0.37; (5)ACD/LogD (pH 7.4): 0.37; (6)ACD/BCF (pH 5.5): 1.13; (7)ACD/BCF (pH 7.4): 1.13; (8)ACD/KOC (pH 5.5): 37.87; (9)ACD/KOC (pH 7.4): 37.87; (10)#H bond acceptors: 0; (11)#H bond donors: 0; (12)#Freely Rotating Bonds: 0; (13)Density: 2.22 g/cm3; (14)Melting point: 447 °C; (15)Boiling point: 2300 °C; (16)Enthalpy of Vaporization: 21.12 kJ/mol; (17)Vapour Pressure: 69700 mmHg at 25 °C.
Preparation of Calcium carbide: this chemical produced industrially in an electric arc furnace from a mixture of lime and coke at approximately 2000 °C:
CaO + 3 C → CaC2 + CO
Uses of Calcium carbide: this chemical is used in the desulfurisation of iron. It can also be used in steelmaking as a fuel to extend the scrap ratio to liquid iron, and as a powerful deoxidizer at ladle treatment facilities. Moreover, it is used in carbide lamps. It is also used in the ripening of fruit as source of acetylene gas. Additionally, it can be used in toy cannons. The product can be used in floating, self-igniting naval signal flares together with calcium phosphide. Furthermore, it is used in the industrial manufacture of Acetylene:
CaC2 + 2 H2O → C2H2 + Ca(OH)2
Similarly, it can used to produce Calcium cyanamide which is used as fertilizer:
CaC2 + N2 → CaCN2 + C
People can use the following data to convert to the molecule structure.
(1)SMILES: [Ca+2].[C-]#[C-]
(2)InChI: InChI=1/C2.Ca/c1-2;/q-2;+2
(3)InChIKey: UIXRSLJINYRGFQ-UHFFFAOYAI
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