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10025-91-9

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10025-91-9 Usage

Chemical Properties

Different sources of media describe the Chemical Properties of 10025-91-9 differently. You can refer to the following data:
1. Colourless Crystal Or Flakes,fuming in moist air.
2. Antimony trichloride is a noncombustible, clear, colorless, crystalline solid. Acrid, pungent odor.

Physical properties

Colorless crystalline solid; orthorhombic crystal; hygroscopic; density 3.14 g/cm3; melts at 73.4°C; boils at 220.3°C; readily dissolves in water undergoing hydrolysis; soluble in dilute hydrochloric acid, ethanol, acetone, benzene, dioxane and CS2.

Uses

Different sources of media describe the Uses of 10025-91-9 differently. You can refer to the following data:
1. Used in the chemical microscopy of drugs.
2. Bronzing iron, especially gun barrels; mordant for patent leather and in dyeing; coloring zinc black; manufacture of lakes, particularly from dye woods; furniture polishes.
3. Antimony Trichloride is used as a chlorinating agent, as a fireproofing agent in textiles; in bronzing steel and as a mordant in dyeing as well as a caustic in medicine. It is also used as an apoptosis agent that is used to detect cholesterols and carotenoids.

Definition

Different sources of media describe the Definition of 10025-91-9 differently. You can refer to the following data:
1. ChEBI: An inorganic chloride salt with formula SbCl3. It is used as a reagent for detecting vitamin A and related carotenoids, reacting with the carotenoid to form a blue complex that can be measured by colorimetry (the Carr-Price test). Solu ions of antimony trichloride were formerly used for dissolving and removing horn stubs from calves and goats.
2. A white deliquescent solid, formerly known as butter of antimony. It is prepared by direct combination of antimony and chlorine. It is readily hydrolyzed by cold water to form a white precipitate of antimony(III) chloride oxide (antimonyl chloride, SbOCl): SbCl3 + H2O = SbOCl + 2HCl.

Preparation

SbCl3 is prepared by reaction of chlorine with antimony, antimony trioxide or antimony trisulfide. It also may be made by treating antimony trioxide with concentrated hydrochloric acid.

General Description

Antimony trichloride is a colorless crystalline solid. Antimony trichloride is shipped as a solid or liquid solution. Antimony trichloride is decomposed slowly by water to hydrochloric acid and antimony oxychloride. Antimony oxychloride is soluble in hydrochloric acid but insoluble in water. Antimony trichloride is corrosive to metals and tissue.

Air & Water Reactions

Fumes in air to form hydrochloric acid [Merck 11th ed. 1989]. Decomposed by water to form hydrochloric acid and antimony oxychloride.

Reactivity Profile

Acidic salts, such as ANTIMONY TRICHLORIDE, are generally soluble in water. The resulting solutions contain moderate concentrations of hydrogen ions and have pH's of less than 7.0. They react as acids to neutralize bases. These neutralizations generate heat, but less or far less than is generated by neutralization of inorganic acids, inorganic oxoacids, and carboxylic acid. They usually do not react as either oxidizing agents or reducing agents but such behavior is not impossible. Many of these compounds catalyze organic reactions.

Hazard

Corrosive liquid or solid. Very irritating to eyes, skin.

Health Hazard

TOXIC; inhalation, ingestion or contact (skin, eyes) with vapors, dusts or substance may cause severe injury, burns or death. Reaction with water or moist air will release toxic, corrosive or flammable gases. Reaction with water may generate much heat that will increase the concentration of fumes in the air. Fire will produce irritating, corrosive and/or toxic gases. Runoff from fire control or dilution water may be corrosive and/or toxic and cause pollution.

Fire Hazard

Non-combustible, substance itself does not burn but may decompose upon heating to produce corrosive and/or toxic fumes. Vapors may accumulate in confined areas (basement, tanks, hopper/tank cars etc.). Substance will react with water (some violently), releasing corrosive and/or toxic gases and runoff. Contact with metals may evolve flammable hydrogen gas. Containers may explode when heated or if contaminated with water.

Flammability and Explosibility

Nonflammable

Safety Profile

Moderately toxic by ingestion. Human pulmonary system effects by inhalation. Corrosive by vigorous reaction with moisture, generating heat and hydrogen chloride gas (a strong irritant), whch can cause pulmonary edema when inhaled. Systemic effects can be caused by the antimony. See also ANTIMONY COMPOUNDS. Experimental reproductive effects. Mutation data reported. When heated to decomposition it emits very toxic fumes of chlorine and antimony. It can react violently with aluminum, potassium, sodmm.

Potential Exposure

It is used to make antimony salts and drugs; to fireproof textiles; and as a catalyst in many organic reactions; as a reagent for chloral, aromatic hydrocarbons, vitamin A, and for drug identification.

Shipping

UN1733 Antimony trichloride, Hazard class: 8; Labels: 8-Corrosive material.

Purification Methods

Dry the trichloride over P2O5 or by mixing it with toluene or xylene and distilling (water is carried off with the organic solvent), then distil it twice under dry nitrogen at 50mm, and sublime it twice in a vacuum into ampoules and seal. It can be crystallised from CS2 and is deliquescent. It fumes in moist air and is decomposed by H2O with precipitation of the basic chloride, but forms a clear solution in dilute HCl.

Incompatibilities

Decomposes in water, forming hydrochloric acid and antimony oxychloride. Reacts violently with strong bases; ammonia, alkali metals; aluminum, potassium, sodium. Forms explosive mixture with perchloric acid when hot. Reacts with air forming hydrochloric acid. Attacks metals in the presence of moisture, forming explosive hydrogen gas.

Waste Disposal

Consult with environmental regulatory agencies for guidance on acceptable disposal practices. Generators of waste containing this contaminant (≥100 kg/mo) must conform with EPA regulations governing storage, transportation, treatment, and waste disposal.

Check Digit Verification of cas no

The CAS Registry Mumber 10025-91-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,0,2 and 5 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 10025-91:
(7*1)+(6*0)+(5*0)+(4*2)+(3*5)+(2*9)+(1*1)=49
49 % 10 = 9
So 10025-91-9 is a valid CAS Registry Number.
InChI:InChI=1/3ClH.Sb.3H/h3*1H;;;;/q;;;+3;;;/p-3/r3ClH.H3Sb/h3*1H;1H3/q;;;+3/p-3

10025-91-9 Well-known Company Product Price

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  • Alfa Aesar

  • (40372)  Antimony(III) chloride, Puratronic?, 99.999% (metals basis)   

  • 10025-91-9

  • 2g

  • 527.0CNY

  • Detail
  • Alfa Aesar

  • (40372)  Antimony(III) chloride, Puratronic?, 99.999% (metals basis)   

  • 10025-91-9

  • 10g

  • 2525.0CNY

  • Detail
  • Alfa Aesar

  • (43449)  Antimony(III) chloride, ultra dry, 99.999% (metals basis)   

  • 10025-91-9

  • 25g

  • 1167.0CNY

  • Detail
  • Alfa Aesar

  • (43449)  Antimony(III) chloride, ultra dry, 99.999% (metals basis)   

  • 10025-91-9

  • 100g

  • 2907.0CNY

  • Detail
  • Alfa Aesar

  • (43449)  Antimony(III) chloride, ultra dry, 99.999% (metals basis)   

  • 10025-91-9

  • 500g

  • 14828.0CNY

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  • Alfa Aesar

  • (A11944)  Antimony(III) chloride, 99+%   

  • 10025-91-9

  • 100g

  • 269.0CNY

  • Detail
  • Alfa Aesar

  • (A11944)  Antimony(III) chloride, 99+%   

  • 10025-91-9

  • 500g

  • 851.0CNY

  • Detail
  • Alfa Aesar

  • (A11944)  Antimony(III) chloride, 99+%   

  • 10025-91-9

  • 2500g

  • 3259.0CNY

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  • Alfa Aesar

  • (41537)  Antimony(III) chloride, 99.9% (metals basis)   

  • 10025-91-9

  • 25g

  • 541.0CNY

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  • Alfa Aesar

  • (41537)  Antimony(III) chloride, 99.9% (metals basis)   

  • 10025-91-9

  • 100g

  • 1590.0CNY

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  • Alfa Aesar

  • (36281)  Antimony(III) chloride, ACS, 99.0% min   

  • 10025-91-9

  • 50g

  • 322.0CNY

  • Detail
  • Alfa Aesar

  • (36281)  Antimony(III) chloride, ACS, 99.0% min   

  • 10025-91-9

  • 250g

  • 1084.0CNY

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10025-91-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name antimony trichloride

1.2 Other means of identification

Product number -
Other names Antimony(III) chloride

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
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:10025-91-9 SDS

10025-91-9Synthetic route

antimony
7440-36-0

antimony

arsenic trichloride
7784-34-1

arsenic trichloride

A

arsenic

arsenic

B

antimony(III) chloride
10025-91-9

antimony(III) chloride

Conditions
ConditionsYield
at 200°C for 6 h; under CO2;A n/a
B 97%
antimony(V) chloride
7647-18-9

antimony(V) chloride

A

antimony
7440-36-0

antimony

B

antimony(III) chloride
10025-91-9

antimony(III) chloride

Conditions
ConditionsYield
With hydrogen In neat (no solvent) in a reversed chlorine detonating gas flame;;A 93%
B 7%
1-bromo-butane
109-65-9

1-bromo-butane

tri(p-tolyl)antimony
5395-43-7

tri(p-tolyl)antimony

A

p-butyltoluene
1595-05-7

p-butyltoluene

B

antimony(III) chloride
10025-91-9

antimony(III) chloride

Conditions
ConditionsYield
With aluminium trichloride In carbon disulfide byproducts: Al(OH)3; hydrolysis;A 80%
B n/a
(2-ClC6H4)2SbCl
112117-70-1

(2-ClC6H4)2SbCl

{2-ClC6H4N2}SbCl4={2-ClC6H4N2}Cl*SbCl3

{2-ClC6H4N2}SbCl4={2-ClC6H4N2}Cl*SbCl3

A

antimony(III) chloride
10025-91-9

antimony(III) chloride

B

tris(2-chlorophenyl)stibine dichloride
125688-58-6

tris(2-chlorophenyl)stibine dichloride

Conditions
ConditionsYield
In acetone byproducts: N2; in cold acetone;A n/a
B 73%
In acetone byproducts: N2; in cold acetone;A n/a
B 73%
antimony(III) trioxide

antimony(III) trioxide

chloro-trimethyl-silane
75-77-4

chloro-trimethyl-silane

A

antimony chloride

antimony chloride

B

antimony(III) chloride
10025-91-9

antimony(III) chloride

C

tris{(trimethylsilyl)oxy}antimony(III)

tris{(trimethylsilyl)oxy}antimony(III)

Conditions
ConditionsYield
In neat (no solvent) byproducts: hexamethyldisilixane; mixture of Sb2O3 and trimethylchlorosilane was stirred at room temp. for1 h; precipitate was filtered off, residue distilled iv vac.;A n/a
B n/a
C 69%
dichlorodimethylaminoborane
1113-31-1

dichlorodimethylaminoborane

antimony(III) fluoride
7783-56-4

antimony(III) fluoride

A

(dimethylamino)difluoroborane
359-18-2

(dimethylamino)difluoroborane

B

antimony(III) chloride
10025-91-9

antimony(III) chloride

Conditions
ConditionsYield
heating at 220°C;A 45%
B n/a
heating at 220°C;A 45%
B n/a
{4-NO2C6H4N2}SbCl4
91159-51-2

{4-NO2C6H4N2}SbCl4

(2-ClC6H4)2SbCl
112117-70-1

(2-ClC6H4)2SbCl

A

antimony(III) chloride
10025-91-9

antimony(III) chloride

B

(2-ClC6H4)2(4-NO2C6H4)SbCl2

(2-ClC6H4)2(4-NO2C6H4)SbCl2

Conditions
ConditionsYield
In acetone byproducts: N2; in cold acetone;A n/a
B 45%
In acetone byproducts: N2; in cold acetone;A n/a
B 45%
Re4N4((CH3)2PC6H5)2Cl2((C2H5)2NCS2)6(SbCl3)2

Re4N4((CH3)2PC6H5)2Cl2((C2H5)2NCS2)6(SbCl3)2

acetonitrile
75-05-8

acetonitrile

A

bis(diethyldithiocarbamato)nitridorhenium(V)
36472-83-0

bis(diethyldithiocarbamato)nitridorhenium(V)

[ReN((CH3)2PC6H5)Cl((C2H5)2NCS2)]4*2CH3CN

[ReN((CH3)2PC6H5)Cl((C2H5)2NCS2)]4*2CH3CN

C

antimony(III) chloride
10025-91-9

antimony(III) chloride

Conditions
ConditionsYield
In acetonitrile reflux for 5 h, with exclusion of moisture; soln. was concd., cooled, crystn. for 12 h, crystals were filtered off, washed with MeCN, elem. anal.;A n/a
B 40%
C n/a
bis(sulfinylamido)tellurane
124824-09-5

bis(sulfinylamido)tellurane

antimonypentachloride
7647-18-9

antimonypentachloride

A

Cl(x)Te(x)

Cl(x)Te(x)

B

NSNSTeCl*Cl*SbCl3 = NSNSTeClClSbCl3

NSNSTeCl*Cl*SbCl3 = NSNSTeClClSbCl3

C

antimony(III) chloride
10025-91-9

antimony(III) chloride

Conditions
ConditionsYield
In dichloromethane byproducts: SO2, N2; stirring mixt. of Te-compd. and SbCl5 (molar ratio 2.1:1.5) in abs. CH2Cl2 at -80°C in a sealed tube (12 h); filtration of pptn. in absence of air and moisture, washing (CH2Cl2), concn. of combined filtrates by removal of solvent in vac. to half of vol., crystn. after few weeks;A n/a
B 1%
C n/a
acetyl chloride
75-36-5

acetyl chloride

Sb2S3

Sb2S3

A

acetyl sulfide
3232-39-1

acetyl sulfide

B

antimony(III) chloride
10025-91-9

antimony(III) chloride

Conditions
ConditionsYield
at 300 - 350℃;
carbon disulfide
75-15-0

carbon disulfide

antimonypentachloride
7647-18-9

antimonypentachloride

A

tetrachloromethane
56-23-5

tetrachloromethane

B

antimony(III) chloride
10025-91-9

antimony(III) chloride

C

sulfur

sulfur

D

disulfur dichloride

disulfur dichloride

triphenylantimony
603-36-1

triphenylantimony

mercury chloride

mercury chloride

A

antimony(III) chloride
10025-91-9

antimony(III) chloride

B

phenylmercury(II) chloride
100-56-1

phenylmercury(II) chloride

hydrogenchloride
7647-01-0

hydrogenchloride

tris(p-anisyl)antimony
21502-70-5

tris(p-anisyl)antimony

A

antimony(III) chloride
10025-91-9

antimony(III) chloride

B

methoxybenzene
100-66-3

methoxybenzene

hydrogenchloride
7647-01-0

hydrogenchloride

triphenyl-phosphine; compound with antimony trichloride

triphenyl-phosphine; compound with antimony trichloride

A

antimony(III) chloride
10025-91-9

antimony(III) chloride

B

triphenylphosphine
603-35-0

triphenylphosphine

tetrachloro-phenyl-phosphorane; antimony pentachloride

tetrachloro-phenyl-phosphorane; antimony pentachloride

A

hydrogenchloride
7647-01-0

hydrogenchloride

B

para-dichlorobenzene
106-46-7

para-dichlorobenzene

C

antimony(III) chloride
10025-91-9

antimony(III) chloride

D

phosphorus trichloride
7719-12-2, 52843-90-0

phosphorus trichloride

Conditions
ConditionsYield
beim Erhitzen;
ammonium nitrate

ammonium nitrate

antimony(III) sulfide

antimony(III) sulfide

ammonium chloride

ammonium chloride

antimony(III) chloride
10025-91-9

antimony(III) chloride

Conditions
ConditionsYield
heated with a mixture of NH4Cl and NH4NO3 (3/1 or 5/1);;
antimony(III) sulfide

antimony(III) sulfide

ammonium chloride

ammonium chloride

A

ammonium sulfide
12135-76-1

ammonium sulfide

B

antimony(III) chloride
10025-91-9

antimony(III) chloride

Conditions
ConditionsYield
boiled in NH4Cl-soln.;;
antimony
7440-36-0

antimony

pyrosulfuryl chloride
7791-27-7

pyrosulfuryl chloride

A

antimony(III) sulfate

antimony(III) sulfate

B

antimony(III) chloride
10025-91-9

antimony(III) chloride

Conditions
ConditionsYield
byproducts: SO2, SO3; dropping S2O5Cl2 to Sb;
antimony(III) selenide

antimony(III) selenide

phosphorus pentachloride
10026-13-8, 874483-75-7

phosphorus pentachloride

A

antimony(III) chloride
10025-91-9

antimony(III) chloride

B

diselenium dichloride
10025-68-0

diselenium dichloride

C

phosphorus trichloride
7719-12-2, 52843-90-0

phosphorus trichloride

Conditions
ConditionsYield
In neat (no solvent) react. on heating;;
phosphonium iodide
164596-64-9

phosphonium iodide

antimonypentachloride
7647-18-9

antimonypentachloride

A

phosphorus
12185-09-0

phosphorus

B

phosphan
7803-51-2

phosphan

C

antimony(III) chloride
10025-91-9

antimony(III) chloride

D

antimony triiodide
7790-44-5

antimony triiodide

Conditions
ConditionsYield
byproducts: HCl; in sealed tube, 100°C;A n/a
B n/a
C >99
D n/a
antimony
7440-36-0

antimony

silver(I) chloride

silver(I) chloride

antimony(III) chloride
10025-91-9

antimony(III) chloride

Conditions
ConditionsYield
In neat (no solvent) heating below melting point of AgCl in vacuum;;
In neat (no solvent) heating below melting point of AgCl in vacuum;;
antimony(III) chloride
10025-91-9

antimony(III) chloride

triphenylantimony
603-36-1

triphenylantimony

diphenylantimony(III) chloride
2629-47-2

diphenylantimony(III) chloride

Conditions
ConditionsYield
In neat (no solvent) for 72h;100%
In neat (no solvent) for 3h;100%
Stage #1: antimony(III) chloride; triphenylantimony at 20℃; for 72h; Inert atmosphere;
Stage #2: for 336h; Cooling;
95%
antimony(III) chloride
10025-91-9

antimony(III) chloride

triphenylantimony
603-36-1

triphenylantimony

dichlorophenylstibine
5035-52-9

dichlorophenylstibine

Conditions
ConditionsYield
In neat (no solvent) for 72h;100%
In neat (no solvent) for 3h;100%
In neat (no solvent) for 3h; Schlenk technique; Inert atmosphere;100%
2-N-(n-butylamino)cyclopentene-1-dithiocarboxylic acid
34281-27-1

2-N-(n-butylamino)cyclopentene-1-dithiocarboxylic acid

antimony(III) chloride
10025-91-9

antimony(III) chloride

antimony(2-butylaminocyclopentenecarbodithioate)3
124183-94-4

antimony(2-butylaminocyclopentenecarbodithioate)3

Conditions
ConditionsYield
In benzene addn. of the carbodithioic acid in benzene to SbCl3 in benzene at room temp. and refluxing for about 8 h; filtn., washing with benzene and drying in vacuo at room temp.; elem. anal.;100%
(C5H5)2(ZrSC3H4)

(C5H5)2(ZrSC3H4)

antimony(III) chloride
10025-91-9

antimony(III) chloride

A

zirconocene dichloride
1291-32-3

zirconocene dichloride

B

Cl(SbSC3H4)
122115-75-7

Cl(SbSC3H4)

Conditions
ConditionsYield
In benzene treatment of the Zr compd. in benzene suspn. with SbCl3 (1 equiv) (25°C); not isolated; detn. by 1H-NMR;A n/a
B 100%
tetraphosphorus decasulfide
15857-57-5

tetraphosphorus decasulfide

pentan-1-ol
71-41-0

pentan-1-ol

antimony(III) chloride
10025-91-9

antimony(III) chloride

antimony tris-(O,O-di-n-pentylphosphorodithioate)
219637-25-9

antimony tris-(O,O-di-n-pentylphosphorodithioate)

Conditions
ConditionsYield
In pentan-1-ol byproducts: H2S, HCl; addn. of P4S10 to pentanol under Ar, stirring at room temp. until H2S evolution ceased (20 h), addn. of SbCl3, stirring at room temp. for 3 h (until HCl evolution stopped); filtn., concentrating the volume of the filtrate under vac., elem. anal.;100%
antimony(III) chloride
10025-91-9

antimony(III) chloride

thiosemicarbazide
79-19-6

thiosemicarbazide

Sb(CH5N3S)Cl3
96928-44-8

Sb(CH5N3S)Cl3

Conditions
ConditionsYield
In 1,4-dioxane soln. of reagents in 1,4-dioxane was heated to 50°C under reflux; ppt. was filtered off, washed with 1,4-dioxane and air-dried, then dried over P2O5 under vac.; elem. anal.;100%
magnesium-anthracene-(THF)3
86901-19-1

magnesium-anthracene-(THF)3

antimony(III) chloride
10025-91-9

antimony(III) chloride

Mg1.51SbCl0.06C1.4H2.8

Mg1.51SbCl0.06C1.4H2.8

Conditions
ConditionsYield
In tetrahydrofuran byproducts: MgCl2, anthracene, THF; Ar atmosphere, addn. of SbCl3 to stirred suspn. of Mg compound, stirring(room temp., 290 h); filtration, washing (THF, pentane), drying (0.1-0.2 mbar); elem. anal.;100%
pentetrazole
54-95-5

pentetrazole

1-ferrocenylmethanol
1273-86-5

1-ferrocenylmethanol

antimony(III) chloride
10025-91-9

antimony(III) chloride

3(4)-(ferrocenylmethylene)-1,5-pentamethylenetetrazolium trichlorohydroxystibate

3(4)-(ferrocenylmethylene)-1,5-pentamethylenetetrazolium trichlorohydroxystibate

Conditions
ConditionsYield
In dichloromethane SbCl3 was added to mixt. of corazol and Fe-complex in CH2Cl2, stirred for 25 min, treated with Et2O, left to stand for 10 d at 4-5°C; filtered, washed with Et2O, dried at room temp.; elem. anal.;100%
pyridine
110-86-1

pyridine

hydrogenchloride
7647-01-0

hydrogenchloride

antimony(III) chloride
10025-91-9

antimony(III) chloride

4-chloro-aniline
106-47-8

4-chloro-aniline

C5H5N*C6H4Cl6Sb(1-)*H(1+)

C5H5N*C6H4Cl6Sb(1-)*H(1+)

Conditions
ConditionsYield
Stage #1: 4-chloro-aniline With sulfuric acid In ethanol for 0.25h; Cooling with ice;
Stage #2: antimony(III) chloride In ethanol for 0.166667h; Cooling with ice;
Stage #3: pyridine; hydrogenchloride Further stages;
100%
antimony(III) chloride
10025-91-9

antimony(III) chloride

1-butyl-3-methylimidazolium chloride
79917-90-1

1-butyl-3-methylimidazolium chloride

3C8H15N2(1+)*Cl6Sb(3-)

3C8H15N2(1+)*Cl6Sb(3-)

Conditions
ConditionsYield
at 120℃; for 4h; Inert atmosphere;100%
antimony(III) chloride
10025-91-9

antimony(III) chloride

trans-1,2-bis(4-pyridyl)ethylene
1135-32-6

trans-1,2-bis(4-pyridyl)ethylene

C12H10N2*Sb(3+)*3Cl(1-)

C12H10N2*Sb(3+)*3Cl(1-)

Conditions
ConditionsYield
In neat (no solvent) for 48h; Inert atmosphere; Sealed tube;100%
4,4'-bipyridine
553-26-4

4,4'-bipyridine

antimony(III) chloride
10025-91-9

antimony(III) chloride

C10H8N2*Sb(3+)*3Cl(1-)

C10H8N2*Sb(3+)*3Cl(1-)

Conditions
ConditionsYield
In neat (no solvent) for 72h; Inert atmosphere; Sealed tube;100%
O,O-di(2-tolyl)dithiophosphoric acid ammonium salt
40783-15-1

O,O-di(2-tolyl)dithiophosphoric acid ammonium salt

antimony(III) chloride
10025-91-9

antimony(III) chloride

[Sb(S2P(OC6H4Me-o)2)3]
1146634-41-4

[Sb(S2P(OC6H4Me-o)2)3]

Conditions
ConditionsYield
In benzene benzene soln. of SbCl3 and NH4S2P(OC6H4Me-o)2 refluxed for 5 h; filtered; vac. evapn.; crystd. from refrigerated hexane soln. after 2-3 d; elem. anal.;99.06%
para-tert-butylphenol
98-54-4

para-tert-butylphenol

antimony(III) chloride
10025-91-9

antimony(III) chloride

sodium
7440-23-5

sodium

Sb{OC6H4C(CH3)3}3

Sb{OC6H4C(CH3)3}3

Conditions
ConditionsYield
In benzene byproducts: NaCl, H2; refluxing of Na and the phenol in THF to a clear and transparent soln., complete removing of THF, drying (reduced pressure), dissolving of the solid in benzene, addn. of SbCl3 in benzene, refluxing (12 h), filtration from pptd. NaCl; removing of excess solvent; elem. anal.;99%
antimony(III) chloride
10025-91-9

antimony(III) chloride

Tri-m-tolyl-stibane
35569-54-1

Tri-m-tolyl-stibane

m-tolylantimony dichloride
165269-23-8

m-tolylantimony dichloride

Conditions
ConditionsYield
In neat (no solvent) Ar atmosphere, stirring (90°C, 2 h), cooling; elem. anal.;99%
antimony(III) tris(O,O′-diisopropyldithiophosphato-S,S′)
1078716-00-3, 84913-97-3, 86118-20-9

antimony(III) tris(O,O′-diisopropyldithiophosphato-S,S′)

antimony(III) chloride
10025-91-9

antimony(III) chloride

bis(O,O′-diisopropyldithiophosphato-S,S′)antimony(III) chloride
85961-69-9

bis(O,O′-diisopropyldithiophosphato-S,S′)antimony(III) chloride

Conditions
ConditionsYield
In benzene for 0.3h; Reflux;99%
In benzene stirring and heating for ca 2 h (mol. ratio 1:2); evapn.; elem. anal.;86%
antimony(III) chloride
10025-91-9

antimony(III) chloride

tri(o-tolyl)antimony
23822-15-3

tri(o-tolyl)antimony

o-tolylantimony dichloride
165269-24-9

o-tolylantimony dichloride

Conditions
ConditionsYield
In neat (no solvent) Ar atmosphere, stirring (90°C, 2 h), cooling; elem. anal.;99%
3,5-Di-tert-butylcatechol

3,5-Di-tert-butylcatechol

antimony(III) chloride
10025-91-9

antimony(III) chloride

2-chloro-1,3-dioxa-4,6-di-t-butylbenzo-2-stibolane
212206-03-6

2-chloro-1,3-dioxa-4,6-di-t-butylbenzo-2-stibolane

Conditions
ConditionsYield
In chloroform-d1 N2, Schlenk tube; mixing stoich. amts. of Sb-compd. and org. compd. solns.; elem. anal.;99%
In toluene for 48h; Reflux; Inert atmosphere;
zirconocene 1,3-diphosphabicyclo[1.1.0]butane
109613-89-0

zirconocene 1,3-diphosphabicyclo[1.1.0]butane

antimony(III) chloride
10025-91-9

antimony(III) chloride

ClSbP2(CC(CH3)3)2
916903-68-9

ClSbP2(CC(CH3)3)2

Conditions
ConditionsYield
In hexane standard Schlenk line and glovebox techniques, Zr-compd. dissolved in n-hexane, reacted with two equiv. SbCl3 at room temp. for 2 h; filtered, stored for 16 h at -15°C;99%
1,5-bis(4-hydroxy-3-methoxybenzaldehyde)carbohydrazone
206141-58-4

1,5-bis(4-hydroxy-3-methoxybenzaldehyde)carbohydrazone

antimony(III) chloride
10025-91-9

antimony(III) chloride

Sb((C6H3(OH)(OCH3)CHNNH)2CO)Cl3
100327-63-7

Sb((C6H3(OH)(OCH3)CHNNH)2CO)Cl3

Conditions
ConditionsYield
In benzene addn. of carbohydrazone to soln. of SbCl3 in dry benzene (molar ratio 1:1), refluxed (110°C bath temp., 12 h); filtered, washed (repeatedly with warm anhydrous alcohol), dried under vac. at 40°C; elem. anal.;99%
antimony(III) chloride
10025-91-9

antimony(III) chloride

sulfur
7704-34-9

sulfur

magnesium
7439-95-4

magnesium

ethylenediamine
107-15-3

ethylenediamine

Mg(NH2CH2CH2NH2)3(2+)*Sb4S7(2-)=Mg(NH2CH2CH2NH2)3Sb4S7

Mg(NH2CH2CH2NH2)3(2+)*Sb4S7(2-)=Mg(NH2CH2CH2NH2)3Sb4S7

Conditions
ConditionsYield
In ethylenediamine High Pressure; solvothermal synthesis; Mg, SbCl3, S, ethylenediamine heated in a sealedTeflon-lined stainless steel autoclave at 170°C for 10 d; coolin g to room temp.; filtered off; washed with H2O, EtOH, acetone; elem. anal.;99%
2-naphthalenylmagnesium bromide
21473-01-8

2-naphthalenylmagnesium bromide

antimony(III) chloride
10025-91-9

antimony(III) chloride

tri(2-naphthyl)stibine
52762-83-1

tri(2-naphthyl)stibine

Conditions
ConditionsYield
In tetrahydrofuran Inert atmosphere;99%
Dimethylarsinic acid
75-60-5

Dimethylarsinic acid

antimony(III) chloride
10025-91-9

antimony(III) chloride

tris(dimethylarsinato)antimony

tris(dimethylarsinato)antimony

Conditions
ConditionsYield
In acetone at 20℃; for 5h;99%
antimony(III) chloride
10025-91-9

antimony(III) chloride

chlorobenzene
108-90-7

chlorobenzene

triphenylantimony
603-36-1

triphenylantimony

Conditions
ConditionsYield
Stage #1: chlorobenzene With cis-Octadecenoic acid; sodium In toluene at 30 - 40℃; for 2h; Inert atmosphere;
Stage #2: antimony(III) chloride In toluene at 110℃; for 3.5h; Solvent; Reagent/catalyst; Temperature; Inert atmosphere;
98.1%
carbonodihydrazide
497-18-7

carbonodihydrazide

antimony(III) chloride
10025-91-9

antimony(III) chloride

Sb(NH2NHCONHNH2)Cl3
100308-28-9

Sb(NH2NHCONHNH2)Cl3

Conditions
ConditionsYield
In benzene addn. of carbohydrazide to soln. of SbCl3 in dry benzene (molar ratio 1:1), mixt. stirred (40°C, 20 h), cream coloured ppt.; filtered, washed (repeatedly with warm anhydrous alcohol), dried under vac. at 40°C; elem. anal.;98%
bis[[2-hydroxyphenyl]methylene]carbonic dihydrazide
6638-49-9

bis[[2-hydroxyphenyl]methylene]carbonic dihydrazide

antimony(III) chloride
10025-91-9

antimony(III) chloride

Sb((C6H4OHCHNNH)2CO)2Cl2(1+)*Cl(1-)={Sb((C6H4OHCHNNH)2CO)2Cl2}Cl
100308-39-2

Sb((C6H4OHCHNNH)2CO)2Cl2(1+)*Cl(1-)={Sb((C6H4OHCHNNH)2CO)2Cl2}Cl

Conditions
ConditionsYield
In benzene addn. of carbohydrazone to soln. of SbCl3 in dry benzene (molar ratio 2:1), colour change from white to pale yellow at room temp., refluxed (110°C bath temp., 12 h); filtered, washed (repeatedly with warm anhydrous alcohol), dried under vac. at 40°C; elem. anal.;98%
antimony(III) chloride
10025-91-9

antimony(III) chloride

Thiocarbohydrazide
2231-57-4

Thiocarbohydrazide

trichloro-thiocarbohydrazide-antimony
90981-52-5

trichloro-thiocarbohydrazide-antimony

Conditions
ConditionsYield
In benzene ligand soln. added to SbCl3 soln. in molar ratio 1/1, refluxed for 10 h; filtered, washed with anhyd. alc., dried (vac.) at 35°C; elem. anal.;98%
antimony(III) chloride
10025-91-9

antimony(III) chloride

bis[[2-hydroxyphenyl]methylene]carbonothioic dihydrazide

bis[[2-hydroxyphenyl]methylene]carbonothioic dihydrazide

trichloro-(1,5-bis(2-hydroxybenzaldehyde)thiocarbohydrazene)-antimony
90994-28-8

trichloro-(1,5-bis(2-hydroxybenzaldehyde)thiocarbohydrazene)-antimony

Conditions
ConditionsYield
In benzene ligand soln. added to SbCl3 soln. in molar ratio 1/1, refluxed for 10 h; filtered, washed with anhyd. alc., dried (vac.) at 35°C; elem. anal.;98%
chlorobis(trimethylsilyl)methane
5926-35-2

chlorobis(trimethylsilyl)methane

antimony(III) chloride
10025-91-9

antimony(III) chloride

tris(bis(trimethylsilyl)methyl)antimony
86509-04-8

tris(bis(trimethylsilyl)methyl)antimony

Conditions
ConditionsYield
With Li In tetrahydrofuran; diethyl ether soln. of ligand in THF was added with stirring to Li in Et2O for 1 h, stirred for 24 h with reflux, filtered, added at room temp. to SbCl3 in Et2O, stirred for 16 h at room temp. under Ar; solvent was removed under reduced pressure, extd. with petroleum ether, solvent was removed, sublimated at 110°C/6E-3 mbar;98%
antimony(III) tris(O,O-di-n-propyl phosphorodithioate)
64923-90-6

antimony(III) tris(O,O-di-n-propyl phosphorodithioate)

antimony(III) chloride
10025-91-9

antimony(III) chloride

dichloroantimony(III) di(n-propyl)dithiophosphate
85961-68-8

dichloroantimony(III) di(n-propyl)dithiophosphate

Conditions
ConditionsYield
In benzene stirring and heating for ca 2 h (mol. ratio 2:1); evapn.; elem. anal.;98%

10025-91-9Relevant articles and documents

Reactivity of Sulphuryl Chloride in Acetonitrile with the Elements

Woolf, Alfred A.

, p. 3325 - 3330 (1991)

Sulphuryl chloride in MeCN reacts with all but the most refractory elements to give mainly solvated chlorides at or below 300 K in contrast with SO2Cl2 alone which requires at least twice this temperature.There is evidence for an ionic mechanism based on analogy, thermochemistry, transport measurements and additive effects.The instability of these solutions leading to polymerization, together with its inhibition, is described.Sulphur dioxide formed in reactions seldom plays a reductive role apart from influencing formation of the mixed-valence Tl4Cl6.Semiquantitative kinetic measurements in different solvents emphasize the uniqueness of MeCN.For most elements attack is diffusion controlled across surface films giving a parabolic dependence on time which can be linearized if film growth is prevented by changing the solvent mix.The varied nature of these surface films vitiates any simple relation between rate and periodicity.Some applications are indicated.

North, H. B.,Conover, C. B.

, p. 2486 - 2490 (1915)

Reversible Isomerization of Cyclo-octasulfur Monoxide; Preparation and X-Ray Crystal Structure of S8O*SbCl5

Steudel, Ralf,Sandow, Torsten,Steidel, Juergen

, p. 180 - 181 (1980)

The reaction of S8O and SbCl5 in CS2 gave S8O*SbCl5 (71percent yield) which was shown by X-ray crystallography to contain S8O in an isomeric conformation compared with pure S8O which can be recovered from the adduct in its usual conformation by recrystall

New method of tris(trimethylsilyl) antimonite preparation

Basenko,Voronkov,Meihua, Cao,Gebel'

, p. 1633 - 1634 (2008)

-

Synthesis, Isolation and Structures of Trifluoromethylated Fullerenes D2-C76, C76(1)(CF3)10–18

Tamm, Nadezhda B.,Ignat'eva, Daria V.,Aslanov, Leonid A.,Troyanov, Sergey I.

, p. 2027 - 2030 (2018)

High-temperature trifluoromethylation of fullerene C76 chlorination products followed by HPLC separation of C76(CF3)n derivatives resulted in the isolation and X-ray structural characterization of thirteen Csub

Reaction of C60 with SbCl5

Daters, W. R.,Ummat, P. K.,Olech, T.,Nkum, R. K.

, p. 579 - 582 (1993)

C60 was doped with SbCl5 by the direct reaction with liquid SbCl5 or with SbCl5 dissolved in CCl4. Mass spectrometer analysis showed that the compound consisted of Cl2, SbCl3 and C60. The SbCl5 was removed by sublimation leaving Cl2 in C60. The doped compound was electrically conducting at room temperature. The resistivity increased with decreasing temperature corresponding to a semiconducting energy gap of 1.1 eV.

Lead-Free Hybrid Material with an Exceptional Dielectric Phase Transition Induced by a Chair-to-Boat Conformation Change of the Organic Cation

Han, Shiguo,Zhang, Jing,Sun, Zhihua,Ji, Chengmin,Zhang, Weichuan,Wang, Yuyin,Tao, Kewen,Teng, Bing,Luo, Junhua

, p. 13078 - 13085 (2017)

Hybrid organic-inorganic perovskite materials have demonstrated great potential in the field of photovoltaics and photoelectronics. On the basis of the high degree of structural flexibility and compatibility, diverse molecular functional materials have been assembled by modifying the length of the organic components and/or dimensionality of the inorganic frameworks. In this paper, we present a chiral lead-free organic-inorganic hybrid, (piperidinium)2SbCl5 (1), which follows the one-dimensional inorganic frameworks of the corner-sharing SbCl6 octahedra. Strikingly, 1 displays a dielectric phase transition at Tc = 338 K, changing from the chiral space group of P212121 to polar Pna21 upon heating. Crystal structure analyses reveal that an unusual thermally activated conformation change of the piperidinium cations affords the driving force to the phase transition of 1. That is, organic piperidinium moieties display a chairlike conformation below Tc, which transforms to a boatlike structure above Tc. Such an unprecedented change is strongly coupled to the dielectric transition along with notable steplike anomalies, which suggest that 1 could be used as a potential switchable dielectric material. Besides, the temperature-dependent conductivity and theoretical analysis of its electronic structure disclose the semiconducting behavior of 1. This study paves the pathway to the design of new lead-free semiconducting perovskites with targeted properties for optoelectronic application.

Booth, H. S.,Herrmann, C. V.

, p. 63 - 66 (1936)

Sandwich-Type Uranyl Phosphate-Polyoxometalate Cluster Exhibiting Strong Luminescence

Kong, Xiang-Jian,Long, La-Sheng,Wang, Hai-Ying,Zheng, Lan-Sun,Zheng, Xiu-Ying

, p. 6790 - 6795 (2021)

A pure inorganic uranyl phosphate-polyoxometalate of Na17{Na@[(SbW9O33)2(UO2)6(PO3OH)6]}·xH2O (abbreviated as Na@U6P6, with x ≈ 46) featuring a sandwich-type structure was prepared using Keggin-type trilacunary [α-B-SbW9O33]9- units as building blocks, which were formed in situ by SbCl3 and Na2WO4·2H2O. Crystal structural analysis showed that six UO22+ cations and six PO3OH2- anions generated a wheel-like cluster unit with a Na+ center ([Na@(UO2)6(PO3OH)6]+) that is stabilized by two [α-B-SbW9O33]9- units. Na@U6P6 displayed a solid-state photoluminescence quantum yield of 33% at 300 K. The temperature-dependent fluorescence emission spectra showed that Na@U6P6 has temperature-sensitive fluorescence in which its emission intensity decreased by 77% as the temperature increased from 200 to 300 K. These results suggest that such uranyl phosphate-polyoxometalate clusters could serve as potential temperature-sensitive molecular materials.

Unexpected product formed by the reaction of [2,6-(MeOCH2)2C6H3]Li with SbCl3: Structure of Sb-O intramolecularly coordinated organoantimony cation

Dostál, Libor,Jambor, Roman,Císa?ová, Ivana,Bene?, Ludvík,R??i?ka, Ale?,Jirásko, Robert,Hole?ek, Jaroslav

, p. 2350 - 2353 (2007)

Reaction of [2,6-(MeOCH2)2C6H3]Li (1) with SbCl3 in 1:1 molar ratio yielded except the intended product [2,6-(MeOCH2)2C6H3]SbCl2 (2) unexpected c

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