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W359602

Sigma-Aldrich

3,4-二甲苯酚

≥98%, FG

同義詞:

3,4-二甲酚, 4-羟基邻二甲苯

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About This Item

線性公式:
(CH3)2C6H3OH
CAS號碼:
分子量::
122.16
FEMA號碼:
3596
Beilstein:
1099267
EC號碼:
歐洲委員會號碼:
11262
MDL號碼:
分類程式碼代碼:
12164502
PubChem物質ID:
Flavis號碼:
4.048
NACRES:
NA.21

生物源

synthetic

等級

FG
Fragrance grade
Halal

agency

follows IFRA guidelines
meets purity specifications of JECFA

法律遵循

EU Regulation 1223/2009
EU Regulation 1334/2008 & 872/2012

化驗

≥98%

bp

227 °C (lit.)

應用

flavors and fragrances

文件

see Safety & Documentation for available documents

食物過敏原

no known allergens

香料過敏原

no known allergens

感官的

burnt

SMILES 字串

Cc1ccc(O)cc1C

InChI

1S/C8H10O/c1-6-3-4-8(9)5-7(6)2/h3-5,9H,1-2H3

InChI 密鑰

YCOXTKKNXUZSKD-UHFFFAOYSA-N

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應用


  • Green Aromatic Epoxidation with an Iron Porphyrin Catalyst for One-Pot Functionalization of Renewable Xylene, Quinoline, and Acridine.: This study explores the green epoxidation of aromatic compounds using an iron porphyrin catalyst, demonstrating effective one-pot functionalization of renewable xylene derivatives, including 3,4-xylenol (Corrêa et al., 2023).

  • A highly expressed odorant receptor from the yellow fever mosquito, AaegOR11, responds to (+)- and (-)-fenchone and a phenolic repellent.: This research identifies an odorant receptor in mosquitoes that responds to various compounds, including 3,4-dimethylphenol, which could have implications for developing new repellents (Lu et al., 2022).


訊號詞

Danger

危險分類

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

儲存類別代碼

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

水污染物質分類(WGK)

WGK 3

閃點(°F)

230.0 °F - closed cup

閃點(°C)

110 °C - closed cup

個人防護裝備

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges


分析證明 (COA)

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V Shingler et al.
Journal of bacteriology, 174(3), 711-724 (1992-02-01)
The meta-cleavage pathway for catechol is one of the major routes for the microbial degradation of aromatic compounds. Pseudomonas sp. strain CF600 grows efficiently on phenol, cresols, and 3,4-dimethylphenol via a plasmid-encoded multicomponent phenol hydroxylase and a subsequent meta-cleavage pathway.

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