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Merck
CN

W358908

Resorcinol

≥98%, FG

别名:

1,3-苯二酚

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关于此项目

线性分子式:
C6H4-1,3-(OH)2
化学文摘社编号:
108-46-3
分子量:
110.11
FEMA Number:
3589
Council of Europe no.:
11250
UNSPSC Code:
12164502
PubChem Substance ID:
24901799
Flavis number:
4.047
EC Number:
203-585-2
NACRES:
NA.21
MDL number:
MFCD00002269
Beilstein/REAXYS Number:
906905
Organoleptic:
creamy; musty
Grade:
FG, Halal
Biological source:
synthetic
Agency:
meets purity specifications of JECFA

主要文件

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SMILES string

Oc1cccc(O)c1

InChI

1S/C6H6O2/c7-5-2-1-3-6(8)4-5/h1-4,7-8H

InChI key

GHMLBKRAJCXXBS-UHFFFAOYSA-N

biological source

synthetic

grade

FG, Halal

agency

meets purity specifications of JECFA

reg. compliance

EU Regulation 1334/2008 & 872/2012, FDA 21 CFR 110

vapor density

3.8 (vs air)

vapor pressure

1 mmHg ( 21.1 °C)

assay

≥98%

form

flakes

autoignition temp.

1126 °F

Quality Level

300

solubility

H2O: 5%, colorless to faintly yellow

application(s)

flavors and fragrances

documentation

see Safety & Documentation for available documents

organoleptic

creamy; musty

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相关类别

signalword

Danger

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 3 - Eye Dam. 1 - Skin Irrit. 2 - Skin Sens. 1B - STOT SE 1 Oral - STOT SE 2 Oral

target_organs

Central nervous system,Blood, Respiratory system

存储类别

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

wgk

WGK 2

flash_point_f

260.6 °F - closed cup

flash_point_c

127 °C - closed cup

ppe

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

法规信息

危险化学品
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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
SHBS8202
SHBR5942
SHBR5820
SHBP5995
SHBP2994

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Anton V Gulevich et al.
Journal of the American Chemical Society, 134(12), 5528-5531 (2012-03-15)
The efficient Pd-catalyzed double-fold C-H oxygenation of arenes into resorcinols using the newly developed 2-pyrimidyldiisopropylsilyl (PyrDipSi) directing group is described. Its use allows for the sequential introduction of OAc and OPiv groups in a one-pot manner to produce orthogonally protected
Phosphate-functionalized carbon monoliths from deep eutectic solvents and their use as monolithic electrodes in supercapacitors.
Daniel Carriazo et al.
ChemSusChem, 5(8), 1405-1409 (2012-07-06)
Antonio B Fuertes et al.
Chemical communications (Cambridge, England), 48(49), 6124-6126 (2012-05-15)
Core@shell spheres made up of a thin layer of resorcinol-formaldehyde enveloping a silica core were prepared by means of a one-step method under Stöber conditions. These spheres are used as a platform for the synthesis of carbon or polymeric capsules
S L da Silva et al.
European journal of medicinal chemistry, 44(1), 312-321 (2008-04-22)
Phospholipases A(2) are enzymes responsible for the hydrolysis of membrane phospholipids that release arachidonic acid, which serves as substrate for pro-inflammatory mediators, such as prostaglandins and leucotriens. The design of specific inhibitors for PLA(2) might help in the development of
Carsten Goebel et al.
Regulatory toxicology and pharmacology : RTP, 64(3), 459-465 (2012-10-17)
With the availability of the local lymph node assay, and the ability to evaluate effectively the relative skin sensitizing potency of contact allergens, a model for quantitative-risk-assessment (QRA) has been developed. This QRA process comprises: (a) determination of a no-expected-sensitisation-induction-level
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