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Merck
CN

31669

氯化锡(II) 二水合物

puriss. p.a., ACS reagent, reag. ISO, reag. Ph. Eur., ≥98%

别名:

氯化亚锡 二水合物

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关于此项目

线性分子式:
SnCl2 · 2H2O
化学文摘社编号:
分子量:
225.65
NACRES:
NA.21
PubChem Substance ID:
UNSPSC Code:
12352302
EC Number:
231-868-0
MDL number:
Assay:
≥98%
Form:
fine crystals
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Quality Level

agency

USP/NF, reag. ISO, reag. Ph. Eur.

grade

ACS reagent, puriss. p.a.

assay

≥98%

form

fine crystals

impurities

≤0.002% ammonium (NH4), ≤0.005% insoluble in hydrochloric acid, ≤0.01% other heavy metals (as Pb), ≤0.05% subst. not precip. by H2S (SO4)

bp

652 °C (lit.)

mp

37-38 °C (dec.) (lit.)

anion traces

sulfate (SO42-): ≤20 mg/kg

cation traces

As: ≤1 mg/kg, Ca: ≤50 mg/kg, Cu: ≤10 mg/kg, Fe: ≤20 mg/kg, K: ≤50 mg/kg, Mg: ≤50 mg/kg, Mn: ≤5 mg/kg, Na: ≤50 mg/kg, Ni: ≤5 mg/kg, Pb: ≤50 mg/kg

SMILES string

O.O.Cl[SnH2]Cl

InChI

1S/2ClH.2H2O.Sn/h2*1H;2*1H2;/q;;;;+2/p-2

InChI key

FWPIDFUJEMBDLS-UHFFFAOYSA-L

General description

氯化锡(II)二水合物是锡(II)的水合盐。它的晶体是单斜晶体,并且人们通过单晶 X 射线衍射方法研究了它们的结构。已报道的电池参数为:a=9.313、b=7.250、c=8.970Å、β=114°55′ 和 Z=4。

Application

氯化锡(II)二水合物可用于以下研究:
  • 吲哚的合成。
  • 醛的制备。
  • 作为路易斯酸催化剂,通过多组分反应,用于3-氨基咪唑并 [1,2-a] 吡啶的合成。


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Danger

Hazard Classifications

Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Aquatic Chronic 3 - Eye Dam. 1 - Met. Corr. 1 - Skin Corr. 1B - Skin Sens. 1 - STOT RE 2 Oral - STOT SE 3

target_organs

Cardio-vascular system, Respiratory system

存储类别

8B - Non-combustible corrosive hazardous materials

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable



历史批次信息供参考:

分析证书(COA)

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Hedieh Saffari et al.
Mayo Clinic proceedings, 95(3), 449-458 (2020-03-07)
To determine if heparin labeled with 99mTechnetium (99mTc) could be an imaging probe to detect eosinophil-related inflammation in eosinophilic esophagitis and to determine the biodistribution and radiation dosimetry of 99mTc-heparin oral administration using image-based dosimetry models with esophageal modeling. Freshly
An X-Ray Redetermination of the Crystal Structure of Tin (II) Chloride Dihydrate.
Kiriyama H, et al.
BuMed News Letter, 46(5), 1389-1395 (1979)
Anupam Bandyopadhyay et al.
Organic & biomolecular chemistry, 8(21), 4855-4860 (2010-08-25)
A facile synthetic route for the preparation of N-protected γ-amino β-keto esters from amino aldehydes and ethyl diazoacetate is described. The two component coupling is facilitated by tin(II) chloride followed by semipinacol rearrangement leading to the product in quantitative yield.



全球贸易项目编号

货号GTIN
31669-100G04061838820402
31669-500G04061826691168
31669-50G-KC04061824020441