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Merck
CN

43540

邻苯二甲酸二异丁酯

certified reference material, TraceCERT®, Manufactured by: Sigma-Aldrich Production GmbH, Switzerland

别名:

DIBP

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关于此项目

线性分子式:
C6H4-1,2-[CO2CH2CH(CH3)2]2
化学文摘社编号:
分子量:
278.34
Beilstein:
2054802
EC 号:
MDL编号:
UNSPSC代码:
41116107
PubChem化学物质编号:
NACRES:
NA.24
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等级

certified reference material
TraceCERT®

质量水平

产品线

TraceCERT®

保质期

limited shelf life, expiry date on the label

制造商/商品名称

Manufactured by: Sigma-Aldrich Production GmbH, Switzerland

技术

HPLC: suitable
gas chromatography (GC): suitable

折射率

n20/D 1.49 (lit.)

沸点

327 °C (lit.)

密度

1.039 g/mL at 25 °C (lit.)

应用

cleaning products
cosmetics
environmental
food and beverages
personal care

包装形式

neat

储存温度

2-8°C

SMILES字符串

CC(C)COC(=O)c1ccccc1C(=O)OCC(C)C

InChI

1S/C16H22O4/c1-11(2)9-19-15(17)13-7-5-6-8-14(13)16(18)20-10-12(3)4/h5-8,11-12H,9-10H2,1-4H3

InChI key

MGWAVDBGNNKXQV-UHFFFAOYSA-N

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一般描述

This certified reference material (CRM) is produced and certified in accordance with ISO/IEC 17025 and ISO 17034. This CRM is traceable to primary material from an NMI, e.g. NIST or NMIJ.
Certified content by quantitative NMR incl. uncertainty and expiry date are given on the certificate.
Download your certificate at: http://www.sigma-aldrich.com.
This compound is listed in the SVHC (Substances of very high concern) candidate list of ECHA (European Chemicals Agency)

应用

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

包装

Bottomless glass bottle. Contents are inside inserted fused cone.

其他说明

Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.

法律信息

TraceCERT is a registered trademark of Merck KGaA, Darmstadt, Germany

象形图

Health hazardEnvironment

警示用语:

Danger

危险声明

危险分类

Aquatic Acute 1 - Aquatic Chronic 1 - Repr. 1B

储存分类代码

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 3

闪点(°F)

228.2 °F - closed cup

闪点(°C)

109 °C - closed cup

法规信息

危险化学品
此项目有

分析证书(COA)

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Kembra L Howdeshell et al.
Toxicological sciences : an official journal of the Society of Toxicology, 105(1), 153-165 (2008-04-16)
Phthalate diesters are chemicals to which humans are ubiquitously exposed. Exposure to certain phthalates during sexual differentiation causes reproductive tract malformations in male rats. In the fetal rat, exposure to the phthalates benzylbutyl phthalate (BBP), di(n)butyl phthalate (DBP), and diethylhexyl
Du Yung Kim et al.
International journal of environmental research and public health, 17(22) (2020-11-25)
Plasticizers are added to diverse consumer products including children's products. Owing to their potential for endocrine disruption, the use of phthalate plasticizers is restricted in many children's products. In this study, exposure to five phthalate esters (dibutylphthalate, di(2-ethylhexyl) phthalate (DEHP)
A M Saillenfait et al.
Toxicology letters, 165(1), 39-46 (2006-03-07)
The developmental toxicity of diisobutyl phthalate (DIBP) was studied in Sprague-Dawley rats after oral administration. Pregnant rats were given DIBP at doses of 0 (olive oil), 250, 500, 750, and 1000 mg/kg/day, by gavage (5 ml/kg), on gestational days (GD)
Kyunghee Ji et al.
Environmental research, 110(4), 375-382 (2010-03-17)
Diet is purported to be means of exposure to many environmental contaminants. The purpose of this study is to understand the influence of dietary change on the levels of exposure to several environmental chemicals - in particular, antibiotics and phthalates.
Anne-Marie Saillenfait et al.
Reproductive toxicology (Elmsford, N.Y.), 26(2), 107-115 (2008-08-19)
Diisobutyl phthalate (DIBP) is the branched isomer of DBP; DBP side chains have a four-carbon backbone (C4), whereas DIBP has its four-carbon alkyl side chains rearranged into a three-carbon backbone (C3) with a methyl branch. Di-n-butyl phthalate (DBP), and several

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