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Supelco

3,5-二叔丁基-4-羟基甲苯

analytical standard

同義詞:

3,5-二叔丁基-4-羟基甲苯, E321

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About This Item

CAS號碼:
EC號碼:
MDL號碼:
分類程式碼代碼:
12164500
PubChem物質ID:

等級

analytical standard

品質等級

CofA

current certificate can be downloaded

包裝

pkg of 500 mg

技術

HPLC: suitable
gas chromatography (GC): suitable

應用

cleaning products
cosmetics
food and beverages
personal care

形式

neat

儲存溫度

room temp

SMILES 字串

Cc1cc(c(O)c(c1)C(C)(C)C)C(C)(C)C

InChI

1S/C15H24O/c1-10-8-11(14(2,3)4)13(16)12(9-10)15(5,6)7/h8-9,16H,1-7H3

InChI 密鑰

NLZUEZXRPGMBCV-UHFFFAOYSA-N

基因資訊

一般說明

3,5-二--4-丁羟甲苯属于酚醛类抗氧化剂,可作为食品及油、脂肪和黄油等其他产品的添加剂,用于防止不饱和脂肪氧化引起的酸败。

應用

3,5-二--4-丁羟甲苯还可作为分析参考标准品,通过色谱法定量测定桉木中的分析物。
有关合适仪器技术的更多信息,请参考产品的分析证书。如需进一步支持,请联系技术服务。

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象形圖

Environment

訊號詞

Warning

危險聲明

防範說明

危險分類

Aquatic Acute 1 - Aquatic Chronic 1

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 2

閃點(°F)

260.6 °F - open cup

閃點(°C)

127 °C - open cup

個人防護裝備

dust mask type N95 (US), Eyeshields, Gloves


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分析證明 (COA)

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存取文件庫

Supercritical fluid extraction of phenolic compounds from Eucalyptus globulus Labill bark
Santos.O.AS, et al.
Journal of Supercritical Fluids, 71, 71-79 (2012)
Ultra-high performance liquid chromatography coupled to mass spectrometry applied to the identification of valuable phenolic compounds from Eucalyptus wood
Santos.O.AS, et al.
Journal of Chromatography. B, Biomedical Sciences and Applications, 938, 65-74 (2013)
Santo Scalia et al.
Molecules (Basel, Switzerland), 18(1), 574-587 (2013-01-08)
The catechin (-)-epigallocatechin-3-gallate (EGCG) exhibits high antioxidant activity and it has been reported to provide protection of the skin against damage induced by solar UV radiation. However, EGCG is highly unstable under sunlight. The present study aimed to compare the
Sol Rivera et al.
Molecules (Basel, Switzerland), 17(9), 11255-11268 (2012-09-25)
We performed a number of tests with the aim to develop an effective extraction method for the analysis of carotenoid content in maize seed. Mixtures of methanol-ethyl acetate (6:4, v/v) and methanol-tetrahydrofuran (1:1, v/v) were the most effective solvent systems
Norhayati Muhammad et al.
Molecules (Basel, Switzerland), 17(8), 9043-9055 (2012-08-01)
A new resveratrol dimer, acuminatol (1), was isolated along with five known compounds from the acetone extract of the stem bark of Shorea acuminata. Their structures and stereochemistry were determined by spectroscopic methods, which included the extensive use of 2D

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HPLC Analysis of Phenolic Antioxidants on Ascentis® Express C18 2.7 μm

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