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Key Documents

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Safety Information

24-0200

Sigma-Aldrich

Pandy′s reagent

Synonym(s):

Phenol solution

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About This Item

Empirical Formula (Hill Notation):
C6H6O
CAS Number:
108-95-2
Molecular Weight:
94.11
Beilstein:
6428463
EC Number:
203-632-7
MDL number:
MFCD00002143
UNSPSC Code:
12352002
PubChem Substance ID:
329752544

form

liquid

availability

available only in Japan

concentration

in H2O

SMILES string

Oc1ccccc1

InChI

1S/C6H6O/c7-6-4-2-1-3-5-6/h1-5,7H

InChI key

ISWSIDIOOBJBQZ-UHFFFAOYSA-N

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Signal Word

Danger

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Aquatic Chronic 2 - Eye Dam. 1 - Muta. 2 - Skin Corr. 1B - STOT RE 2

Target Organs

Nervous system,Kidney,Liver,Skin

WGK

WGK 2

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

PDSCL

Deleterious substance

ISHL Indicated Name

Substances Subject to be Indicated Names

ISHL Notified Names

Substances Subject to be Notified Names

JAN Code

24-0200-6-100ML-J:
24-0200-5-500ML-J:
24-0200-2-25ML-J:

Certificates of Analysis (COA)

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B K Shormanov et al.
Sudebno-meditsinskaia ekspertiza, 56(2), 33-37 (2013-06-27)
The present work was designed to study the specific features of 2-methyl hydroxybezene and 3-methyl hydroxybenzene distribution after intragastric administration of these toxicants to warm-blooded animals (rats). They were detected in the unmetabolized form in the internal organs and blood
Cintia E Paisio et al.
Environmental technology, 34(1-4), 485-493 (2013-03-28)
The use of native microorganisms is a useful strategy for phenol bioremediation. In the present work, a bacterial strain, named RTE1.4, was isolated from effluents of a chemical industry. The strain was able to grow at high concentrations of phenol
Qi Zhang et al.
Dalton transactions (Cambridge, England : 2003), 42(12), 4175-4184 (2013-02-07)
A systematic theoretical study on the Rh-catalyzed oxidative Heck-coupling of phenol carbamates with alkenes is carried out. Two possible mechanisms (i.e. arene activation-first and alkene activation-first mechanisms) are examined. As to the C-H activation step, four mechanisms including oxidative addition
Yanxue Han et al.
Journal of environmental management, 118, 196-204 (2013-03-05)
In this work, the surface structures of biochars, derived from three types of biomass, switchgrass (SG), hardwood (HW) and softwood (SW) through either fast pyrolysis (FP) in a fluidized-bed reactor (at 500 °C) or slow pyrolysis (at 500° and 700 °C), were
Kolishka V Tsekova et al.
Zeitschrift fur Naturforschung. C, Journal of biosciences, 68(1-2), 53-59 (2013-05-11)
The capability of cells of the fungus Aspergillus awamori, either free or immobilized in hybrid sol-gel material cells, for phenol biodegradation was demonstrated. Phenol was present in the reaction mixture as the sole carbon and energy source, and its decomposition
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