Welcome to LookChem.com Sign In|Join Free

CAS

  • or

2720-73-2

Post Buying Request

2720-73-2 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • Potassium Amylxanthate CAS 2720-73-2 AMYLXANTHIC ACID POTASSIUM SALT CAS no 2720-73-2 potassium O-pentyl dithiocarbonate

    Cas No: 2720-73-2

  • USD $ 3.5-5.0 / Kiloliter

  • 5 Kiloliter

  • 3000 Metric Ton/Month

  • Chemwill Asia Co., Ltd.
  • Contact Supplier

2720-73-2 Usage

Chemical Properties

Potassium Amylxanthate is an organosulfur compound, pale yellow powder with a pungent odor, soluble in water. It is widely used in flotation processes used in the mining industry to separate ores.

Uses

Potassium Amylxanthate can be used as collector in metal beneficiation.

Preparation

Potassium amylxanthate is prepared by reacting n-amyl alcohol with CS2 and KOH.CH3(CH2)4OH + CS2 + KOH→CH3(CH2)4OCS2K+H2O

Flammability and Explosibility

Flammable

Check Digit Verification of cas no

The CAS Registry Mumber 2720-73-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,7,2 and 0 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 2720-73:
(6*2)+(5*7)+(4*2)+(3*0)+(2*7)+(1*3)=72
72 % 10 = 2
So 2720-73-2 is a valid CAS Registry Number.
InChI:InChI=1/C11H18N2O3.C3H6OS2.K.Na/c1-4-6-7(3)11(5-2)8(14)12-10(16)13-9(11)15;1-2-4-3(5)6;;/h7H,4-6H2,1-3H3,(H2,12,13,14,15,16);2H2,1H3,(H,5,6);;/q;;2*+1/p-1

2720-73-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name potassium,pentoxymethanedithioate

1.2 Other means of identification

Product number -
Other names Potassium pentylxanthate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Processing aids, not otherwise listed,Solids separation agents
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:2720-73-2 SDS

2720-73-2Synthetic route

carbon disulfide
75-15-0

carbon disulfide

pentan-1-ol
71-41-0

pentan-1-ol

potassium amylxanthate
2720-73-2

potassium amylxanthate

Conditions
ConditionsYield
With potassium hydroxide In diethyl ether at 20℃; for 3h;95%
Stage #1: pentan-1-ol With potassium hydroxide for 4h; Schlenk technique; Inert atmosphere;
Stage #2: carbon disulfide Schlenk technique; Inert atmosphere;
75.9%
With potassium hydroxide In Petroleum ether
Stage #1: pentan-1-ol With potassium hydroxide for 1h; Reflux;
Stage #2: carbon disulfide
Stage #1: pentan-1-ol With potassium hydroxide for 0.666667h;
Stage #2: carbon disulfide at 30℃; for 2h;
potassium amylxanthate
2720-73-2

potassium amylxanthate

cadmium(II) chloride
10108-64-2

cadmium(II) chloride

bis(n-pentylxanthato)cadmium(II)

bis(n-pentylxanthato)cadmium(II)

Conditions
ConditionsYield
In water at 20℃; Schlenk technique; Inert atmosphere;87%
potassium amylxanthate
2720-73-2

potassium amylxanthate

zinc(II) chloride
7646-85-7

zinc(II) chloride

zinc(II)-O-pentan-1-yl-dithiocarbonate

zinc(II)-O-pentan-1-yl-dithiocarbonate

Conditions
ConditionsYield
In water for 2h;86.1%
In water at 20℃; Schlenk technique; Inert atmosphere;78.8%
potassium amylxanthate
2720-73-2

potassium amylxanthate

4-chlorobenzoylmethyl bromide
536-38-9

4-chlorobenzoylmethyl bromide

O-Pentyl-S-(4-chlor-phenacyl)-dithiocarbonat
1861-73-0

O-Pentyl-S-(4-chlor-phenacyl)-dithiocarbonat

Conditions
ConditionsYield
In acetone for 0.5h; Heating;83.4%
potassium amylxanthate
2720-73-2

potassium amylxanthate

2-bromo-1-(3-bromo-4-chlorophenyl)ethanone
87427-58-5

2-bromo-1-(3-bromo-4-chlorophenyl)ethanone

Dithiocarbonic acid S-[2-(3-bromo-4-chloro-phenyl)-2-oxo-ethyl] ester O-pentyl ester

Dithiocarbonic acid S-[2-(3-bromo-4-chloro-phenyl)-2-oxo-ethyl] ester O-pentyl ester

Conditions
ConditionsYield
In acetonitrile for 0.5h; Heating;81.6%
potassium amylxanthate
2720-73-2

potassium amylxanthate

para-bromophenacyl bromide
99-73-0

para-bromophenacyl bromide

O-Pentyl-S-(4-brom-phenacyl)-dithiocarbonat
1861-53-6

O-Pentyl-S-(4-brom-phenacyl)-dithiocarbonat

Conditions
ConditionsYield
In acetone for 0.5h; Heating;78.8%
potassium amylxanthate
2720-73-2

potassium amylxanthate

acetophenone
98-86-2

acetophenone

pentyl 2-oxo-2-phenylacetate
31197-64-5

pentyl 2-oxo-2-phenylacetate

Conditions
ConditionsYield
With iodine; dimethyl sulfoxide In water at 80℃; for 12h; Schlenk technique;78%
potassium amylxanthate
2720-73-2

potassium amylxanthate

molybdenum pentakis(pentylxanthate)

molybdenum pentakis(pentylxanthate)

Conditions
ConditionsYield
With molybdenum(V) chloride In dichloromethane; water for 0.5h;68%
molybdenum(V) chloride
10241-05-1

molybdenum(V) chloride

potassium amylxanthate
2720-73-2

potassium amylxanthate

molybdenum (IV) n-pentyloxyxanthate

molybdenum (IV) n-pentyloxyxanthate

Conditions
ConditionsYield
In dichloromethane; water for 0.5h;65%
cyclopentadienyl titanium(IV) trichloride
1270-98-0

cyclopentadienyl titanium(IV) trichloride

potassium amylxanthate
2720-73-2

potassium amylxanthate

(C5H5)Ti(S2COC5H11)Cl2
93939-53-8

(C5H5)Ti(S2COC5H11)Cl2

Conditions
ConditionsYield
In dichloromethane taking CpTiCl3 and potassium alkyl xanthate in 1:1 molar ratio and adding CH2Cl2 followed by reflux for 22 h; soln. filtered, volume reduced, dry petroleum ether (60-80°C) added and allowed to stand overnight, crystals filtered and dried at 80°C; elem. anal.;48%
cyclopentadienyl titanium(IV) trichloride
1270-98-0

cyclopentadienyl titanium(IV) trichloride

potassium amylxanthate
2720-73-2

potassium amylxanthate

(C5H5)Ti(S2COC5H11)3
93939-55-0

(C5H5)Ti(S2COC5H11)3

Conditions
ConditionsYield
In dichloromethane taking CpTiCl3 and potassium alkyl xanthate in 1:3 molar ratio and adding CH2Cl2 followed by reflux for 40 h; soln. filtered, volume reduced, dry petroleum ether (60-80°C) added and allowed to stand overnight, crystals filtered and dried at 80°C; elem. anal.;48%
cyclopentadienyl titanium(IV) trichloride
1270-98-0

cyclopentadienyl titanium(IV) trichloride

potassium amylxanthate
2720-73-2

potassium amylxanthate

(C5H5)Ti(S2COC5H11)2Cl
93939-54-9

(C5H5)Ti(S2COC5H11)2Cl

Conditions
ConditionsYield
In dichloromethane taking CpTiCl3 and potassium alkyl xanthate in 1:2 molar ratio and adding CH2Cl2 followed by reflux for 25 h; soln. filtered, volume reduced, dry petroleum ether (60-80°C) added and allowed to stand overnight, crystals filtered and dried at 80°C; elem. anal.;46%
2-chloroethyl ethyl ether
628-34-2

2-chloroethyl ethyl ether

potassium amylxanthate
2720-73-2

potassium amylxanthate

S-(2-Ethoxyethyl)-O-amyl-dithiocarbonat
53594-89-1

S-(2-Ethoxyethyl)-O-amyl-dithiocarbonat

2-chloroethyl-n-propylsulfide
4303-42-8

2-chloroethyl-n-propylsulfide

potassium amylxanthate
2720-73-2

potassium amylxanthate

Dithiocarbonic acid O-pentyl ester S-(2-propylsulfanyl-ethyl) ester
41256-04-6

Dithiocarbonic acid O-pentyl ester S-(2-propylsulfanyl-ethyl) ester

Conditions
ConditionsYield
In ethanol
butyl-(2-chloro-ethyl)-sulfide
4303-40-6

butyl-(2-chloro-ethyl)-sulfide

potassium amylxanthate
2720-73-2

potassium amylxanthate

S-2-Butylthioaethyl-O-pentyl-dithiocarbonat
41256-06-8

S-2-Butylthioaethyl-O-pentyl-dithiocarbonat

Conditions
ConditionsYield
In ethanol
triethylchloromethylsilane
757-34-6

triethylchloromethylsilane

potassium amylxanthate
2720-73-2

potassium amylxanthate

Triethylsilylmethylxanthogensaeure-pentylester
22118-26-9

Triethylsilylmethylxanthogensaeure-pentylester

Conditions
ConditionsYield
In ethanol
potassium amylxanthate
2720-73-2

potassium amylxanthate

Diisopropyl chlorophosphate
2574-25-6

Diisopropyl chlorophosphate

Phosphorsaeure-diisopropylester-pentylxanthogenat
109100-44-9

Phosphorsaeure-diisopropylester-pentylxanthogenat

Conditions
ConditionsYield
In diethyl ether
potassium amylxanthate
2720-73-2

potassium amylxanthate

dipropyl chlorophosphate
2510-89-6

dipropyl chlorophosphate

Dipropyl-phosphorsaeure-pentylxanthogenat
109100-42-7

Dipropyl-phosphorsaeure-pentylxanthogenat

Conditions
ConditionsYield
In diethyl ether
potassium amylxanthate
2720-73-2

potassium amylxanthate

propargyl bromide
106-96-7

propargyl bromide

Prop-2-inyl-xanthogensaeure-pentylester
22118-19-0

Prop-2-inyl-xanthogensaeure-pentylester

Conditions
ConditionsYield
In ethanol
potassium amylxanthate
2720-73-2

potassium amylxanthate

A

carbon disulfide
75-15-0

carbon disulfide

B

pentan-1-ol
71-41-0

pentan-1-ol

Conditions
ConditionsYield
With hydrogenchloride In water at 35.1℃; Kinetics; Mechanism; Thermodynamic data; ΔH(excit.), ΔS(excit.), ΔF(excit.); further temperature; further acid concentrations;
potassium amylxanthate
2720-73-2

potassium amylxanthate

n-amyl dixanthogen
869-91-0

n-amyl dixanthogen

Conditions
ConditionsYield
With iron(III) perchlorate In acetonitrile Ambient temperature; determination of amount by potentiometric or spectrophotometric titration;
potassium amylxanthate
2720-73-2

potassium amylxanthate

bis(O-pentylxanthato)nickel(II)
61160-30-3

bis(O-pentylxanthato)nickel(II)

Conditions
ConditionsYield
In methanol; water excess methanolic Ni-acetate; recrystn. from ethanol;
In methanol; water excess methanolic Ni-acetate; recrystn. from ethanol;
nickel(II)

nickel(II)

potassium amylxanthate
2720-73-2

potassium amylxanthate

bis(O-pentylxanthato)nickel(II)
61160-30-3

bis(O-pentylxanthato)nickel(II)

Conditions
ConditionsYield
In water react. of Ni(2+) with alkylxanthate ions in aq. soln.; washing by decantation, filtration, drying in air;
silver (I) ion
14701-21-4

silver (I) ion

potassium amylxanthate
2720-73-2

potassium amylxanthate

dithiocarbonic acid O-pentylester; silver-salt

dithiocarbonic acid O-pentylester; silver-salt

Conditions
ConditionsYield
In ethanol; water in acidic soln.;
potassium amylxanthate
2720-73-2

potassium amylxanthate

uranyl ion
16637-16-4

uranyl ion

UO2(S2COn-C5H11)2

UO2(S2COn-C5H11)2

Conditions
ConditionsYield
In water
In water
potassium amylxanthate
2720-73-2

potassium amylxanthate

germanium dioxide

germanium dioxide

germanyl bis(amylxanthate) * H2O

germanyl bis(amylxanthate) * H2O

Conditions
ConditionsYield
In water byproducts: KOH; mixed; allowed to stand (1 d, pH=6.5); filtered off; washed (ether); dried (75°C; to const. mass); elem.anal.;
potassium amylxanthate
2720-73-2

potassium amylxanthate

bis(O-amyldithiocarbonato)bis(3-methylpyridine)nickel(II)
55173-32-5

bis(O-amyldithiocarbonato)bis(3-methylpyridine)nickel(II)

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: water
2: acetone
View Scheme
potassium amylxanthate
2720-73-2

potassium amylxanthate

bis(O-amyldithiocarbonato)bis(2,4-dimethylpyridine)nickel(II)
1416575-55-7

bis(O-amyldithiocarbonato)bis(2,4-dimethylpyridine)nickel(II)

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: water
2: acetone
View Scheme
potassium amylxanthate
2720-73-2

potassium amylxanthate

bis(O-amyldithiocarbonato)bis(3,4-dimethylpyridine)nickel(II)
1416575-56-8

bis(O-amyldithiocarbonato)bis(3,4-dimethylpyridine)nickel(II)

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: water
2: acetone
View Scheme
potassium amylxanthate
2720-73-2

potassium amylxanthate

bis(O-amyldithiocarbonato)bis(3,5-dimethylpyridine)nickel(II)
1416575-57-9

bis(O-amyldithiocarbonato)bis(3,5-dimethylpyridine)nickel(II)

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: water
2: acetone
View Scheme

2720-73-2Relevant articles and documents

Synthesis and characterization of the adducts of bis(O-amyldithiocarbonato) nickel(II) with nitrogen donors and X-ray structure of bis(O- amyldithiocarbonato)bis (3,5-dimethylpyridine)nickel(II)

Singh, Kuldeep,Neerupama,Kour, Inderjeet,Sachar, Renu,Gupta, Vivek K.,Rajnikant, Verma

, p. 1176 - 1181 (2012)

A series of complexes with general formula M(Xan)2L2 (M = Ni(II), Xan = O-amyldithiocarbonato, L = 3-methylpyridine, 2,4-; 3,4-; 3,5-dimethylpyridines and 2,4,6-trimethylpyridine) have been synthesized and characterized by elemental analysis and various physico-chemical techniques such as magnetic susceptibility measurements, conductivity measurements, UV-Visible, Infrared spectral data. On the basis of electronic spectra and magnetic susceptibility measurements, an octahedral geometry has been proposed for all the complexes. IRspectral data shows that the substituted pyridines in all these complexes coordinate to the metal ion through nitrogen atoms occupying fifth and sixth axial positions where as O-alkyldithiocarbonate act as monoanion bidentate ligand and occupy the planar positions of octahedral structures. The X-ray diffraction analysis of one of the adducts bis(O-amyldithiocarbonato) bis(3,5-dimethylpyridine) nickel(II) is also investigated. The complex crystallizes in the monoclinic space group P21/c with unit cell parameters a = 9.167(2) A, b = 18.255(4) A, c = 9.299(2) A and β = 103.47(2)°. The dihedral angle between dithio-groups and the pyridine ring is 88.9(1)°. The crystal structure of the molecule is stabilized by π-π interactions. Springer Science+Business Media New York 2012.

Production method of high-grade potassium xanthate

-

Paragraph 0022-0024; 0089-0111, (2020/09/12)

The invention discloses a production method of high-grade potassium xanthate. The specific process of the method is as follows: mixing alcohol and flaky alkali, crushing and stirring to obtain a mixedsolution; transferring the mixed solution into a reaction kettle, slowly dropwise adding carbon disulfide, controlling the temperature of the system in the reaction kettle to be 30-35 DEG C in the dropwise adding process, continuously carrying out heat preservation reaction at 30-35 DEG C, and sequentially removing alcohol and drying the reacted system to obtain potassium xanthate. The preparation method comprises the following steps: adding flaky alkali into alcohol and carrying out wet crushing; so that the reaction is promoted, side reactions are reduced, and the conversion rate of materials is increased the grade of the potassium xanthate is increased to 95% or above, the problem that the grade of the potassium xanthate synthesized in the prior art is low is solved, an alkali grindingprocess is avoided, safe production is realized, and the environmental protection and safety pressure is reduced.

VIBRATIONAL ANALYSIS OF ALKYL XANTHATES

Colthup, N. B.,Powell, L. Porter

, p. 317 - 322 (2007/10/02)

Rotational isomers are indicated in the Raman spectra of sodium ethyl and other xanthates.Vibrational bands useful for characterizing xanthate solids and aqueous solutions are given.Vibrational analyses are reported for sodium ethyl xanthate, trans and gauche forms, and the methyl and isopropyl analogs using a Cartesian coordinate force field derived from ab initio molecular orbital calculations.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 2720-73-2