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Merck
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Documenti fondamentali

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30-1840

Sigma-Aldrich

Thionyl chloride

SAJ special grade, ≥95.0%

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About This Item

Formula condensata:
SOCl2
Numero CAS:
7719-09-7
Peso molecolare:
118.97
Beilstein:
1209273
Numero MDL:
MFCD00011449
Codice UNSPSC:
12352307
ID PubChem:
329753343

Grado

SAJ special grade

Tensione di vapore

97 mmHg ( 20 °C)

Saggio

≥95.0%

Stato

liquid

Disponibilità

available only in Japan

Indice di rifrazione

n20/D 1.518 (lit.)

P. ebollizione

79 °C (lit.)

Punto di fusione

−105 °C (lit.)

Densità

1.631 g/mL at 25 °C (lit.)

Temperatura di conservazione

15-25°C

Stringa SMILE

ClS(Cl)=O

InChI

1S/Cl2OS/c1-4(2)3
FYSNRJHAOHDILO-UHFFFAOYSA-N

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Pittogrammi

Skull and crossbonesCorrosion
GHS06,GHS05

Avvertenze

Danger

Indicazioni di pericolo

H302,H314,H331,H335

Classi di pericolo

Acute Tox. 3 Inhalation - Acute Tox. 4 Oral - Eye Dam. 1 - Skin Corr. 1A - STOT SE 3

Organi bersaglio

Respiratory system

Rischi supp

EUH014,EUH029

Codice della classe di stoccaggio

6.1D - Non-combustible acute toxic Cat.3 / toxic hazardous materials or hazardous materials causing chronic effects

Classe di pericolosità dell'acqua (WGK)

WGK 1

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

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Certificati d'analisi (COA)

Lot/Batch Number
A7959
A1132
A0959
A9450
A4626

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Xiangshu Xiao et al.
The Journal of organic chemistry, 70(16), 6496-6498 (2005-07-30)
The indeno[1,2-c]isoquinolines are an important class of topoisomerase I inhibitors with anticancer activity. The condensation of Schiff bases with homophthalic anhydrides provides a mixture of cis- and trans-4-carboxy-3,4-dihydro-3-phenyl-1(2H)isoquinolones. Although the cis products can be readily converted to indeno[1,2-c]isoquinolines with thionyl
S Aksoy et al.
Journal of biotechnology, 60(1-2), 37-46 (1998-05-08)
Poly(methyl methacrylate-acrylic acid) microspheres were prepared and the acid groups were activated by using either carbodiimide (CDI) or thionyl chloride (SOCl2). alpha-Amylase was covalently bound on these activated microspheres. The properties of the immobilized enzyme were investigated and compared with
R Karunanithy et al.
Journal of pharmacobio-dynamics, 12(8), 468-475 (1989-08-01)
The relationships between contraceptive activity, hydrophobic character and alkaline hydrolysis rates were studied in three homologous series of norethisterone and levonorgestrel esters. Hydrophobic character was expressed by the high-performance liquid chromatographic retention term, VR(w) or retention volume at 100% aqueous
N L Benoiton et al.
International journal of peptide and protein research, 43(4), 321-324 (1994-04-01)
Fmoc-glutamic acid is converted by thionyl chloride into the dichloride, which spontaneously cyclizes to Fmoc-pyroglutamyl chloride. The latter is stable to water. Pure Fmoc-pyroglutamyl chloride is obtained by washing the reaction mixture with water, which destroys uncyclized dichloride by converting
Gwenaël Chamoulaud et al.
Langmuir : the ACS journal of surfaces and colloids, 20(12), 4989-4995 (2005-06-30)
This paper describes a novel approach for the surface modification of a cation-exchange membrane, bearing sulfonate groups, by a cationic layer. The modification procedure involved the chlorosulfonation of the sulfonate groups of the base membrane with thionyl chloride, followed by
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