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Merck

G11004

Sigma-Aldrich

愈创奥

99%

别名:

1,4-二甲基-7-异丙基薁

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About This Item

经验公式(希尔记法):
C15H18
CAS号:
分子量:
198.30
Beilstein:
1365001
EC號碼:
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22

化驗

99%

bp

153 °C/7 mmHg (lit.)

mp

27-29 °C (lit.)

密度

0.976 g/mL at 25 °C (lit.)

SMILES 字串

CC(C)c1ccc(C)c2ccc(C)c2c1

InChI

1S/C15H18/c1-10(2)13-7-5-11(3)14-8-6-12(4)15(14)9-13/h5-10H,1-4H3

InChI 密鑰

FWKQNCXZGNBPFD-UHFFFAOYSA-N

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應用

愈创木烯可用作合成
  • 氮杂戊烯基染料分子(如 3-(7-异丙基-1,4-二甲基氮杂戊烯-3-基)-2-氰基丙烯酸和 5-(7-异丙基-1,4-二甲基氮杂戊烯-3-基)-2-氰基戊烯-2,4-二烯酸)的起始物料。
  • Stilbazulenyl nitrone,第二代氮烯基硝酮,可用作断链抗氧化剂。
  • 基于双氮杂戊基的近红外荧光猝灭剂。

象形圖

Exclamation mark

訊號詞

Warning

危險聲明

危險分類

Acute Tox. 4 Oral

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

235.4 °F - closed cup

閃點(°C)

113 °C - closed cup

個人防護裝備

dust mask type N95 (US), Eyeshields, Gloves


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Determination of the ophthalmic drug guaiazulene by high-performance liquid chromatography.
E Vidal-Ollivier et al.
Journal of chromatography, 463(1), 227-228 (1989-01-20)
Jessica Fiori et al.
Toxicology in vitro : an international journal published in association with BIBRA, 25(1), 64-72 (2010-09-22)
Guaiazulene (GA) is widely used as a natural ingredient in many health care products and solutions. Although it has been reported to have interesting biological effects, GA and azulene derivatives have been proven to be cytotoxic against normal human cells
Graziano Guella et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 9(23), 5770-5777 (2003-12-16)
It is shown here that calenzanane sesquiterpenes (1 and 6) can be isolated from organic extracts from the red seaweed Laurencia microcladia Kützing from the Bay of Calenzana, Elba Island, provided contact with acidic media is minimized. Such contact induces
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Reproduction in domestic animals = Zuchthygiene, 46(5), 862-869 (2011-02-18)
Reactive oxygen species (ROS) are between the major contributors for the reduced rate of in vitro bovine embryo production. It is believed that they can cause abnormal meiosis of oocytes, developmental arrest or cell death of embryos. Reports on the
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Journal of agricultural and food chemistry, 60(1), 112-123 (2011-12-14)
Fifteen new guaiazulene-based terpenoids designated anthogorgienes A-O (1-15) were isolated from a Chinese gorgonian Anthogorgia sp., together with eight known analogues (16-23). The structural patterns were classified into monomers, dimers, and trimers, which were supposed to be generated from a

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