357405

Zirconium(IV) chloride

≥99.9% trace metals basis

Manufacturer: Sigma Aldrich

CAS Number: 10026-11-6

Synonym(S): Tetrachlorozirconium, Zirconium tetrachloride

Select a Size

Pack Size SKU Availability Price
10 G 357405-10-G In Stock ₹ 5,791.38
100 G 357405-100-G In Stock ₹ 16,562.25

357405 - 10 G

₹ 5,791.38

In Stock

Quantity

1

Base Price: ₹ 5,791.38

GST (18%): ₹ 1,042.448

Total Price: ₹ 6,833.828

vapor pressure

1 mmHg ( 190 °C)

Quality Level

100

Assay

≥99.9% trace metals basis

form

powder

reaction suitability

reagent type: catalystcore: zirconium

impurities

≤1000.0 ppm Trace Metal Analysis

transition temp

sublimation point 331 °C

density

2.8 g/mL at 25 °C (lit.)

application(s)

battery manufacturing

SMILES string

Cl[Zr](Cl)(Cl)Cl

Other Options

Image Product Name Manufacturer Price Range
NC2380027
Sigma Aldrich Fine Chemicals Biosciences Zirconium(IV) Chloride, ZrCl4 | 99.99% Purity | 100 GR | CAS 10026-11-6 | MDL MFCD00011199
Sigma Aldrich Fine Chemicals Biosciences ₹ 15,931.27
221880
Zirconium(IV) chloride
Sigma Aldrich ₹ 5,315.08 - ₹ 8,421.85
647640
Zirconium(IV) chloride
Sigma Aldrich ₹ 11,052.33 - ₹ 25,211.43
221880
Zirconium(IV) chloride
Sigma Aldrich ₹ 5,315.08 - ₹ 8,421.85
647640
Zirconium(IV) chloride
Sigma Aldrich ₹ 11,052.33 - ₹ 25,211.43
357405
Zirconium(IV) chloride
Sigma Aldrich ₹ 5,791.38 - ₹ 16,562.25
AA01640
10026-11-6 | Zirconium(iv) chloride
A2B Chem ₹ 1,454.52 - ₹ 4,106.88

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Description

  • Application: Zirconium (IV) chloride acts as an efficient Lewis acid catalyst for various reactions; such as:electrophilic addition reaction of indole with aldehydes/ketones to form bis(indolyl)methanes. electrophilic amination of activated arenes,transthioacetylization of acetals,deoxygenation of heterocyclic-N-oxides,reduction of nitro compounds,conversion of carbonyl compounds to 1,3-oxathiolanes,Biginelli reaction for the synthesis of 3,4-dihydropyrimidin-2(1H)-ones,[1]direct amide coupling of non activated carboxylic acids and amines,[2]synthesis of quinoxalines and pyrido[2,3-b]pyrazines,[3]deprotection of t-butyldimethylsilyl (TBDMS) ethers.[4]Activates pyrrolidines for improved conversion, via a modified Bouveault reaction, to the corresponding α,α-dimethylamines.[5]

SAFETY INFORMATION

Pictograms

GHS05

Signal Word

Danger

Hazard Statements

H290,H314

Precautionary Statements

P234 - P260 - P280 - P303 + P361 + P353 - P304 + P340 + P310 - P305 + P351 + P338

Hazard Classifications

Met. Corr. 1 - Skin Corr. 1B

Supplementary Hazards

EUH014,EUH071

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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357405

≥99.9% trace metals basis...


vapor pressure:
1 mmHg ( 190 °C)

Quality Level:
100

Assay:
≥99.9% trace metals basis

form:
powder

reaction suitability:
reagent type: catalystcore: zirconium

impurities:
≤1000.0 ppm Trace Metal Analysis

transition temp:
sublimation point 331 °C

density:
2.8 g/mL at 25 °C (lit.)

application(s):
battery manufacturing

SMILES string:
Cl[Zr](Cl)(Cl)Cl

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