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332070

Sigma-Aldrich

(2,3-环氧丙基)苯

98%

同義詞:

(苯基甲基)环氧乙烷

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About This Item

經驗公式(希爾表示法):
C9H10O
CAS號碼:
分子量::
134.18
MDL號碼:
分類程式碼代碼:
12162002
PubChem物質ID:
NACRES:
NA.23

化驗

98%

形狀

liquid

折射率

n20/D 1.523 (lit.)

bp

98-100 °C/17 mmHg (lit.)

密度

1.02 g/mL at 25 °C (lit.)

SMILES 字串

C1OC1Cc2ccccc2

InChI

1S/C9H10O/c1-2-4-8(5-3-1)6-9-7-10-9/h1-5,9H,6-7H2

InChI 密鑰

JFDMLXYWGLECEY-UHFFFAOYSA-N

象形圖

Exclamation mark

訊號詞

Warning

危險聲明

危險分類

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

標靶器官

Respiratory system

儲存類別代碼

10 - Combustible liquids

水污染物質分類(WGK)

WGK 3

閃點(°F)

179.6 °F - closed cup

閃點(°C)

82 °C - closed cup

個人防護裝備

Eyeshields, Gloves, type ABEK (EN14387) respirator filter


分析證明 (COA)

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T M Guenthner et al.
Toxicology, 160(1-3), 47-58 (2001-03-14)
The genotoxic potential of naturally occurring allylbenzene analogs, including safrole, eugenol, estragole, and others, has been examined in many studies over the past 30 years. It has been established that these compounds are subject to biotransformation in the liver, which
G Luo et al.
Drug metabolism and disposition: the biological fate of chemicals, 24(9), 1020-1027 (1996-09-01)
Epoxidation at the allylic side chain is a major metabolic pathway for allylbenzene and its naturally occurring analogs safrole, estragole, and eugenol. We demonstrate herein that the epoxide metabolites of allylbenzene, estragole, and safrole can form covalent adducts with DNA
G Luo et al.
Drug metabolism and disposition: the biological fate of chemicals, 22(5), 731-737 (1994-09-01)
The enzymatic detoxication in vitro of the 2',3'-epoxide derivatives of allylbenzene and estragole was examined, and the relative rates of enzymatic glutathione conjugation and epoxide hydrolysis were compared with those for styrene 1',2'-oxide. HPLC was used to determine the amounts

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