T36404
o-Toluic acid
99%
Sinonimo/i:
2-Methylbenzoic acid
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About This Item
Formula condensata:
CH3C6H4CO2H
Numero CAS:
Peso molecolare:
136.15
Beilstein:
1072103
Numero CE:
Numero MDL:
Codice UNSPSC:
12352100
ID PubChem:
NACRES:
NA.22
Prodotti consigliati
Saggio
99%
P. ebollizione
258-259 °C (lit.)
Punto di fusione
102-104 °C (lit.)
Densità
1.062 g/mL at 25 °C (lit.)
Stringa SMILE
Cc1ccccc1C(O)=O
InChI
1S/C8H8O2/c1-6-4-2-3-5-7(6)8(9)10/h2-5H,1H3,(H,9,10)
ZWLPBLYKEWSWPD-UHFFFAOYSA-N
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Categorie correlate
Descrizione generale
o-Toluic acid is an aromatic carboxylic acid and an organic intermediate used in pesticides and medicines.
Codice della classe di stoccaggio
11 - Combustible Solids
Classe di pericolosità dell'acqua (WGK)
WGK 3
Punto d’infiammabilità (°F)
298.4 °F - closed cup
Punto d’infiammabilità (°C)
148 °C - closed cup
Dispositivi di protezione individuale
dust mask type N95 (US), Eyeshields, Gloves
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I clienti hanno visto anche
Trine J Meza et al.
Nucleic acids research, 40(14), 6620-6631 (2012-04-26)
The Escherichia coli AlkB protein (EcAlkB) is a DNA repair enzyme which reverses methylation damage such as 1-methyladenine (1-meA) and 3-methylcytosine (3-meC). The mammalian AlkB homologues ALKBH2 and ALKBH3 display EcAlkB-like repair activity in vitro, but their substrate specificities are
Erwin van den Born et al.
Nucleic acids research, 37(21), 7124-7136 (2009-09-30)
The iron(II)- and 2-oxoglutarate (2OG)-dependent dioxygenase AlkB from Escherichia coli (EcAlkB) repairs alkylation damage in DNA by direct reversal. EcAlkB substrates include methylated bases, such as 1-methyladenine (m(1)A) and 3-methylcytosine (m(3)C), as well as certain bulkier lesions, for example the
Damian Mielecki et al.
PloS one, 7(1), e30588-e30588 (2012-02-01)
ALKBH proteins, the homologs of Escherichia coli AlkB dioxygenase, constitute a direct, single-protein repair system, protecting cellular DNA and RNA against the cytotoxic and mutagenic activity of alkylating agents, chemicals significantly contributing to tumor formation and used in cancer therapy.
K H Wang et al.
Chemosphere, 40(4), 389-394 (2000-02-09)
This investigation used UV light of 365 nm and titanium dioxide in aqueous suspension to study the photocatalytic reaction of o-methylbenzoic acid under the influence of pH values, anion additives and the varieties of titanium dioxide. From experimental results, under
Shiu-Mei Liu et al.
Journal of environmental science and health. Part A, Toxic/hazardous substances & environmental engineering, 38(6), 1099-1113 (2003-05-31)
Composition of the headspace gas affected the biotransformation pattern of toluic acid isomers in anoxic sediment slurries. Under an N2 atmosphere, o- and m-, and p-toluic acid (20-25 mg L(-1)) were biotransformed in 100 days, 77 days, and 148 days
Global Trade Item Number
| SKU | GTIN |
|---|---|
| T36404-500G | 4061837344794 |
| T36404-1KG | |
| T36404-5G | |
| T36404-100G | 4061837344787 |
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