推荐产品
等級
certified reference material
TraceCERT®
產品線
TraceCERT®
CofA
current certificate can be downloaded
特點
standard type calibration
包裝
ampule of 1 mL
濃度
2000 μg/mL in methanol: water (4:1)
技術
HPLC: suitable
gas chromatography (GC): suitable
應用
cleaning products
cosmetics
environmental
food and beverages
personal care
格式
single component solution
儲存溫度
-10 to -25°C
SMILES 字串
CI
InChI
1S/CH3I/c1-2/h1H3
InChI 密鑰
INQOMBQAUSQDDS-UHFFFAOYSA-N
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應用
有关合适的仪器技术的更多信息,请参阅产品的分析证书。想要获得更多支持,请联系技术服务部。
其他說明
该有证标准物质(CRM)是根据ISO 17034和ISO/IEC 17025生产和认证的。有关此CRM使用的所有信息均可在分析证书上找到。
法律資訊
TraceCERT is a registered trademark of Merck KGaA, Darmstadt, Germany
訊號詞
Danger
危險分類
Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Flam. Liq. 2 - STOT SE 1
標靶器官
Eyes,Central nervous system
儲存類別代碼
3 - Flammable liquids
水污染物質分類(WGK)
WGK 2
閃點(°F)
50.0 °F - closed cup
閃點(°C)
10 °C - closed cup
其他客户在看
Nature chemistry, 4(7), 534-538 (2012-06-22)
Solvents have a profound influence on chemical reactions in solution and have long been used to control their outcome. Such effects are generally considered to be governed by thermodynamics; however, little is known about the steric effects of solvent molecules.
Microhydration effects on the intermediates of the S(N)2 reaction of iodide anion with methyl iodide.
Angewandte Chemie (International ed. in English), 52(16), 4380-4383 (2013-01-31)
International journal of biological macromolecules, 50(1), 263-269 (2011-11-22)
Five water-soluble chitosan derivatives were carried out by quaternizing either iodomethane or N-(3-chloro-2-hydroxypropyl) trimethylammonium chloride (Quat188) as a quaternizing agent under basic condition. The degree of quaternization (DQ) ranged between 28±2% and 90±2%. The antifungal activity was evaluated by using
Nuclear medicine and biology, 39(1), 89-99 (2011-08-13)
To explore the possible use of positron emission tomography (PET) probes for imaging of I(2)-imidazoline receptors (I(2)Rs) in peripheral tissues, we labeled two new I(2)R ligands, 2-[2-(o-tolyl)vinyl]-4,5-dihydro-1H-imidazole (K(i) for I(2)Rs, 3.7 nM) and 2-[2-(o-tolyl)ethyl]-4,5-dihydro-1H-imidazole (K(i) for I(2)Rs, 1.7 nM) with
Journal of agricultural and food chemistry, 60(7), 1776-1787 (2012-02-09)
The results are reported of a theoretical study of iodomethane (H(3)C-I, 1) and chloropicrin (Cl(3)C-NO(2), 2), of the heterodimers 3-6 formed by aggregation of 1 and 2, and of their addition products 7 and 8 and their possible fragmentation reactions
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