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Merck
CN

12353

Supelco

苯甲酸

reference material for titrimetry, certified by BAM, >99.5%

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关于此项目

线性分子式:
C6H5COOH
化学文摘社编号:
分子量:
122.12
Beilstein:
636131
EC 号:
MDL编号:
UNSPSC代码:
41116107
eCl@ss:
39023903
PubChem化学物质编号:
NACRES:
NA.24
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等级

reference material

质量水平

蒸汽密度

4.21 (vs air)

蒸汽压

10 mmHg ( 132 °C)

方案

>99.5%

自燃温度

1061 °F

质量

certified by BAM

技术

titration: suitable

沸点

249 °C (lit.)

mp

121-125 °C (lit.)

溶解性

water: soluble (2.9 g/l at 25 °C)

密度

1.32 g/cm3 at 20 °C

应用

environmental

包装形式

neat

SMILES字符串

OC(=O)c1ccccc1

InChI

1S/C7H6O2/c8-7(9)6-4-2-1-3-5-6/h1-5H,(H,8,9)

InChI key

WPYMKLBDIGXBTP-UHFFFAOYSA-N

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一般描述

苯甲酸是在严格条件下以最高精度合格的容量法滴定标准品。采用容量中和法作为主要分析方法进行含量测定和同质性评估。

应用

其可作为标准物质,用于在碱量滴定中标定滴定溶液。

特点和优势

  • 以坚固玻璃瓶装固体形式提供,确保开封前整个保质期内的稳定性。
  • 可追溯至 NIST SRM
  • 高品质材料,可提供精准的滴定测定
  • 随附分析证书(CoA)

分析说明

精确浓度、有效期以及认证的详细信息请见每个包装内的证书和认证报告。含量和有效期见标签。

象形图

Health hazardCorrosion

警示用语:

Danger

危险声明

危险分类

Eye Dam. 1 - Skin Irrit. 2 - STOT RE 1 Inhalation

靶器官

Lungs

储存分类代码

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

WGK

WGK 1

个人防护装备

dust mask type N95 (US), Eyeshields, Faceshields, Gloves


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Allen J Duplantier et al.
Journal of medicinal chemistry, 52(11), 3576-3585 (2009-05-15)
3-Hydroxyquinolin-2(1H)-one (2) was discovered by high throughput screening in a functional assay to be a potent inhibitor of human DAAO, and its binding affinity was confirmed in a Biacore assay. Cocrystallization of 2 with the human DAAO enzyme defined the
S Nacht et al.
Journal of the American Academy of Dermatology, 4(1), 31-37 (1981-01-01)
The transepidermal penetration and metabolic disposition of 14C-benzoyl peroxide were assessed in vitro (excised human skin) and in vivo (rhesus monkey). In vitro, the benzoyl peroxide penetrated into the skin, through the stratum corneum or the follicular openings, or both
Ly Dieu Tran et al.
Journal of the American Chemical Society, 134(44), 18237-18240 (2012-10-30)
An auxiliary-assisted, copper catalyzed or promoted sulfenylation of benzoic acid derivative β-C-H bonds and benzylamine derivative γ-C-H bonds has been developed. The method employs disulfide reagents, copper(II) acetate, and DMSO solvent at 90-130 °C. Application of this methodology to the
Wanchun Xiang et al.
ChemSusChem, 6(2), 256-260 (2013-01-25)
Sensing the sun: Incorporation of a cyanomethyl benzoic acid electron acceptor into donor-π-acceptor sensitizers for dye-sensitized-solar cell is shown to lead to devices with improved conversion efficiency when compared with more widely used cyanoacetic acid acceptor.
Copper-mediated C-H/C-H biaryl coupling of benzoic acid derivatives and 1,3-azoles.
Mayuko Nishino et al.
Angewandte Chemie (International ed. in English), 52(16), 4457-4461 (2013-03-21)

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