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Merck

PHR1220

Supelco

二乙醇胺

Pharmaceutical Secondary Standard; Certified Reference Material

别名:

2,2′-亚氨基二乙醇, 二(2-羟乙基)胺

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About This Item

线性分子式:
HN(CH2CH2OH)2
CAS号:
分子量:
105.14
Beilstein:
605315
EC號碼:
MDL號碼:
分類程式碼代碼:
41116107
PubChem物質ID:
NACRES:
NA.24

等級

certified reference material
pharmaceutical secondary standard

品質等級

agency

traceable to USP 1192808

蒸汽密度

3.6 (vs air)

蒸汽壓力

<0.98 atm ( 100 °C)

API 家族

diethanolamine

CofA

current certificate can be downloaded

自燃溫度

689 °F

expl. lim.

10.6 %

技術

HPLC: suitable
gas chromatography (GC): suitable

折射率

n20/D 1.477 (lit.)

bp

217 °C/150 mmHg (lit.)

mp

28 °C (lit.)

密度

1.097 g/mL at 25 °C (lit.)

應用

pharmaceutical (small molecule)

格式

neat

儲存溫度

2-30°C

SMILES 字串

OCCNCCO

InChI

1S/C4H11NO2/c6-3-1-5-2-4-7/h5-7H,1-4H2

InChI 密鑰

ZBCBWPMODOFKDW-UHFFFAOYSA-N

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一般說明

Pharmaceutical secondary standards for application in quality control, provide pharma laboratories and manufacturers with a convenient and cost-effective alternative to the preparation of in-house working standards. Diethanolamine is commonly used as a chemical intermediate and as a surface-active agent in agricultural products, pharmaceutical formulations and cosmetics.

應用

These Secondary Standards are qualified as Certified Reference Materials. These are suitable for use in several analytical applications including but not limited to pharma release testing, pharma method development for qualitative and quantitative analyses, food and beverage quality control testing, and other calibration requirements.

分析報告

These secondary standards offer multi-traceability to the USP, EP (PhEur) and BP primary standards, where they are available.

其他說明

This Certified Reference Material (CRM) is produced and certified in accordance with ISO 17034 and ISO/IEC 17025. All information regarding the use of this CRM can be found on the certificate of analysis.
Ion Mobility: TWCCSN2 value of 119.8 Å2 [M+H]+

The collision cross section (CCS) measurement was provided by Waters Corporation, using the SYNAPT XS mass spectrometer.
For a description and overview of how ion mobility enables the measurement of the CCS of an ion visit ims.waters.com.
Further information on the SYNAPT XS mass spectrometer can be found on the IMS microsite and product webpage.

TWCCS measurements are expected to be within 2% of this reference value.

P/N PHR1220 is part of the Waters Extractables & Leachables UNIFI scientific library which can be downloaded from Waters Marketplace.

腳註

To see an example of a Certificate of Analysis for this material enter LRAC3260 in the slot below. This is an example certificate only and may not be the lot that you receive.

訊號詞

Danger

危險分類

Acute Tox. 4 Oral - Eye Dam. 1 - Repr. 2 - Skin Irrit. 2 - STOT RE 2 Oral

標靶器官

Kidney,Liver,Blood

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 2

閃點(°F)

280.4 °F - closed cup

閃點(°C)

138 °C - closed cup


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分析证书(COA)

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其他客户在看

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Ecotoxicological evaluation of diethanolamine using a battery of microbiotests
Zurita LJ, et al.
Toxicology in vitro, 19(7), 879-886 (2005)
Siou-Yin Chen et al.
Inorganic chemistry, 51(8), 4448-4457 (2012-04-05)
The synthesis, X-ray crystallography, magnetic properties, and high-field electron paramagnetic resonance (HFEPR) of a new heptanuclear manganese complex [Mn(7)(heamp)(6)](ClO(4))(2)·4CH(2)Cl(2)·H(2)O (complex 2), in which heampH(3) is 2-[N,N-di(2-hydroxyethyl)aminomethyl]phenol (compound 1), is reported. Complex 2 has a hexagonal, disk-shaped topology and contains six
William Conway et al.
Environmental science & technology, 46(13), 7422-7429 (2012-05-25)
The kinetics of the fast reversible carbamate formation reaction of CO(2)(aq) with a series of substituted cyclic secondary amines as well as the noncyclic secondary amine diethanolamine (DEA) has been investigated using the stopped-flow spectrophotometric technique at 25.0 °C. The
Honghui Yu et al.
Journal of immunology (Baltimore, Md. : 1950), 193(6), 2902-2910 (2014-08-15)
Anti-D can prevent immunization to the RhD Ag on RBCs, a phenomenon commonly termed Ab-mediated immune suppression (AMIS). The most accepted theory to explain this effect has been the rapid clearance of RBCs. In mouse models using SRBC, these xenogeneic
S H Zeisel et al.
The Biochemical journal, 232(2), 403-408 (1985-12-01)
An understanding of the biosynthesis and metabolism of dimethylamine (DMA) is important because it is a precursor of dimethylnitrosamine (nitroso-DMA). DMA is the major short-chain aliphatic amine in human and rat urine. DMA is formed from trimethylamine (TMA), which, in

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