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Merck
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Documenti

05-2650

Sigma-Aldrich

Cloralio

SAJ special grade, ≥99.7%

Sinonimo/i:

Tricloroacetaldeide

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About This Item

Formula condensata:
Cl3CCH(OH)2
Numero CAS:
302-17-0
Peso molecolare:
165.40
Beilstein:
1698497
Numero CE:
206-117-5
Numero MDL:
MFCD00044479
Codice UNSPSC:
12352100
ID PubChem:
329747671

Grado

SAJ special grade

Saggio

≥99.7%

Disponibilità

available only in Japan

Punto di fusione

57 °C (lit.)

Stringa SMILE

OC(O)C(Cl)(Cl)Cl

InChI

1S/C2H3Cl3O2/c3-2(4,5)1(6)7/h1,6-7H
RNFNDJAIBTYOQL-UHFFFAOYSA-N

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Pittogrammi

Skull and crossbones
GHS06

Avvertenze

Danger

Indicazioni di pericolo

H301,H315,H319

Classi di pericolo

Acute Tox. 3 Oral - Eye Irrit. 2 - Skin Irrit. 2

Codice della classe di stoccaggio

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

Classe di pericolosità dell'acqua (WGK)

WGK 2

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges

Certificati d'analisi (COA)

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Tal I Arnon et al.
PloS one, 3(5), e2150-e2150 (2008-05-15)
The natural cytotoxic receptors (NCRs) are a unique set of activating proteins expressed mainly on the surface of natural killer (NK) cells. The NCRs, which include three members; NKp46, NKp44 and NKp30, are critically involved in NK cytotoxicity against different
Stephanie K West et al.
The British journal of ophthalmology, 97(11), 1437-1442 (2013-09-21)
To report the largest study on the safety and effectiveness of sedation in paediatric ophthalmology in a nurse-led outpatient sedation unit. Retrospective cohort study reviewing all children who underwent sedation from January 2006 to December 2010. Patients were sedated with
A D Steinberg
Pediatrics, 92(3), 442-446 (1993-09-01)
Current federal regulations of potentially carcinogenic environmental chemicals are based on the assumption that risks for humans can be extrapolated from the effects of chronic high-dose exposure of rodents. It is assumed that all chemicals induce cancer by a genotoxic
T L Sourkes
Molecular and chemical neuropathology, 17(1), 21-30 (1992-08-01)
Chloral hydrate was introduced into therapeutics more than 120 years ago, and soon became popular as a somnifacient. It is the first synthetic CNS depressant. Its metabolite, urochloralic acid, was detected early. Studies of the biochemical pharmacology of chloral hydrate
A G Salmon et al.
Journal of toxicology. Clinical toxicology, 33(2), 115-121 (1995-01-01)
Chloral hydrate is commonly used to sedate children for diagnostic or therapeutic procedures. The drug has been extensively used for many years, but there are remarkably few data on its long-term health effects. Concern in this regard is raised by
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