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Merck
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Documentos Principais

A28708

Sigma-Aldrich

Allyl alcohol

99%

Sinônimo(s):

2-Propen-1-ol

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About This Item

Fórmula linear:
CH2=CHCH2OH
Número CAS:
Peso molecular:
58.08
Beilstein:
605307
Número CE:
Número MDL:
NACRES:
NA.24

densidade de vapor

2 (vs air)

pressão de vapor

23.8 mmHg ( 25 °C)

Ensaio

99%

temperatura de autoignição

712 °F

Lim. expl.

18 %

índice de refração

n20/D 1.412 (lit.)

pb

96-98 °C (lit.)

pf

−129 °C (lit.)

densidade

0.854 g/mL at 25 °C (lit.)

cadeia de caracteres SMILES

OCC=C

InChI

1S/C3H6O/c1-2-3-4/h2,4H,1,3H2

chave InChI

XXROGKLTLUQVRX-UHFFFAOYSA-N

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Aplicação

Used to induce a mouse model of liver damage that has been used to study the mechanisms of hepatotoxicity and hepatic stem cell-mediated repair.

Embalagem

18L packaged in Kilo-Lab™ metal cylinders. Cylinder-outlet valve or transfer line needed to dispense material. Cylinders require deposit

Palavra indicadora

Danger

Classificações de perigo

Acute Tox. 2 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Aquatic Acute 1 - Aquatic Chronic 3 - Eye Irrit. 2 - Flam. Liq. 2 - Repr. 2 - Skin Irrit. 2 - STOT SE 3

Órgãos-alvo

Respiratory system

Código de classe de armazenamento

3 - Flammable liquids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

71.6 °F - closed cup

Ponto de fulgor (°C)

22 °C - closed cup


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Taku Chiba et al.
Bioorganic & medicinal chemistry letters, 17(9), 2487-2491 (2007-03-03)
A series of sugar derivatives (7-14) were synthesized from stachyose, a sugar compound of Stachys sieboldi Miq, and evaluated for antibacterial activity against Mycobacterium tuberculosis, Mycobacterium avium, and Staphylococcus aureus, and their structure-activity relationships were studied. The results showed that
Takeki Uehara et al.
Molecular nutrition & food research, 54(2), 218-227 (2009-12-31)
Biotechnology advances have provided novel methods for the risk assessment of chemicals. The application of microarray technologies to toxicology, known as toxicogenomics, is becoming an accepted approach for identifying chemicals with potential safety problems. Gene expression profiling is expected to
Sean Ekins et al.
Drug metabolism and disposition: the biological fate of chemicals, 38(12), 2302-2308 (2010-09-17)
Drug-induced liver injury (DILI) is one of the most important reasons for drug development failure at both preapproval and postapproval stages. There has been increased interest in developing predictive in vivo, in vitro, and in silico models to identify compounds
Nigel Greene et al.
Chemical research in toxicology, 23(7), 1215-1222 (2010-06-18)
Drug-induced liver injury is a major issue of concern and has led to the withdrawal of a significant number of marketed drugs. An understanding of structure-activity relationships (SARs) of chemicals can make a significant contribution to the identification of potential
Zhichao Liu et al.
PLoS computational biology, 7(12), e1002310-e1002310 (2011-12-24)
Drug-induced liver injury (DILI) is a significant concern in drug development due to the poor concordance between preclinical and clinical findings of liver toxicity. We hypothesized that the DILI types (hepatotoxic side effects) seen in the clinic can be translated

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