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Merck
CN

33047

苯甲酸

ACS reagent grade, ≥99.9% (alkalimetric), crystalline, puriss. p.a., reag. Ph. Eur.

别名:

Benzenecarboxylic acid, Carboxybenzene

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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
NACRES:
NA.21
PubChem Substance ID:
eCl@ss:
39023903
UNSPSC Code:
12352100
EC Number:
200-618-2
MDL number:
Beilstein/REAXYS Number:
636131
Assay:
≥99.9% (alkalimetric)
Form:
crystalline
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产品名称

苯甲酸, puriss. p.a., ACS reagent, reag. Ph. Eur., ≥99.9% (alkalimetric)

agency

reag. Ph. Eur.

vapor density

4.21 (vs air)

vapor pressure

10 mmHg ( 132 °C)

grade

ACS reagent, puriss. p.a.

assay

≥99.9% (alkalimetric)

form

crystalline

autoignition temp.

1061 °F

impurities

readily oxidisable substances, in accordance, ≤0.002% S-compounds (as S), ≤0.005% halogen compounds (as Cl), ≤0.005% insoluble in methanol

ign. residue

≤0.005% (as SO4)

bp

249 °C (lit.)

mp

121-125 °C (lit.)

solubility

water: soluble (2.9 g/l at 25 °C)

anion traces

sulfate (SO42-): ≤20 mg/kg

cation traces

Cu: ≤5 mg/kg, Fe: ≤5 mg/kg, Pb: ≤2 mg/kg, Zn: ≤5 mg/kg

functional group

carboxylic acid, phenyl

SMILES string

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

General description

苯甲酸是一种有机芳香族单羧酸。以无色小叶或针状出现。它与氢化试剂反应生成六氢苯甲酸。在石灰或碱中(通过加热)会发生分解,可生成苯和二氧化碳。它可由钴或锰催化的甲苯空气氧化反应合成。

Application

苯甲酸可用作定量和量热研究的标准品。可用作合成以下产品的中间体:
  • 油漆
  • 颜料
  • 涂剂
  • 湿润剂
  • 芳香化合物
  • 苯甲酰氯
  • 苄川三氯


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pictograms

Health hazardCorrosion

signalword

Danger

Hazard Classifications

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

target_organs

Lungs

存储类别

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

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

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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Eagleson M.
Concise Encyclopedia Chemistry, 122-122 (1994)
G C Tremblay et al.
Pharmacology & therapeutics, 60(1), 63-90 (1993-10-01)
Detoxification of sodium benzoate by elimination as a conjugate with glycine, a nonessential amino acid, provides a pathway for the disposal of waste nitrogen. Since 1979, sodium benzoate has been widely used in the therapeutic regimen to combat ammonia toxicity
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



全球贸易项目编号

货号GTIN
33047-100G-R04061826725993
33047-1KG-R04061826726006
33047-250G-R04061826726013