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16101

Sigma-Aldrich

Resorcinol

meets analytical specification of Ph. Eur., BP, 98.5-100.5% (calc. to the dried substance)

Synonyme(s) :

1,3-Benzenediol

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About This Item

Formule linéaire :
C6H4-1,3-(OH)2
Numéro CAS:
Poids moléculaire :
110.11
Numéro Beilstein :
906905
Numéro CE :
Numéro MDL:
Code UNSPSC :
41116107
eCl@ss :
39023402
ID de substance PubChem :
Nomenclature NACRES :
NA.21

Densité de vapeur

3.8 (vs air)

Niveau de qualité

Pression de vapeur

1 mmHg ( 21.1 °C)

Pureté

98.5-100.5% (calc. to the dried substance)

Forme

solid

Température d'inflammation spontanée

1126 °F

Qualité

meets analytical specification of Ph. Eur., BP

Impuretés

acidity or alkalinity, complies
related subst., complies
residual solvents, complies
≤0.001% heavy metals (as Pb)
≤0.01% free acid (as H2SO4)
≤0.01% free alkali (as NH3)
≤0.01% pyrocatechol

Résidus de calcination

≤0.05% (as SO4)

Perte

≤1.0% loss on drying (on silica gel)

Point d'ébullition

178 °C/16 mmHg (lit.)

Pf

109-112 °C (lit.)

Solubilité

water: soluble

Traces d'anions

chloride (Cl-): ≤100 mg/kg
sulfate (SO42-): ≤500 mg/kg

Adéquation

complies for appearance of solution
complies for identity

Application(s)

pharmaceutical (small molecule)

Chaîne SMILES 

Oc1cccc(O)c1

InChI

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

Clé InChI

GHMLBKRAJCXXBS-UHFFFAOYSA-N

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Application

Resorcinol has been used in resorcinol staining for visualizing the gangliosides. It has also been used for estimating sialic acids by colorimetric assay.

Actions biochimiques/physiologiques

Resorcinol is an aromatic alcohol serves as an antiseptic. It reduces pain from painful nodules in patients suffering from Hidradenitis suppurativa (HS).

Mention d'avertissement

Danger

Classification des risques

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

Organes cibles

Central nervous system,Blood, Respiratory system

Code de la classe de stockage

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

Classe de danger pour l'eau (WGK)

WGK 2

Point d'éclair (°F)

260.6 °F - closed cup

Point d'éclair (°C)

127 °C - closed cup

Équipement de protection individuelle

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


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Consulter la Bibliothèque de documents

Elodie Masson et al.
The Biochemical journal, 388(Pt 2), 537-544 (2005-01-19)
Alterations in proliferation and hypertrophy of renal mesangial cells are typical features of diabetic nephropathy. The HP (hexosamine pathway) has been proposed as a biochemical hypothesis to explain microvascular alterations due to diabetic nephropathy; however, involvement of HP in the
J Boer et al.
Clinical and experimental dermatology, 35(1), 36-40 (2009-06-25)
Hidradenitis suppurativa (HS) is a chronic, inflammatory skin disease characterized by abscess formation localized to apocrine sweat gland-bearing skin. The most important factor in patients' overall assessment of disease severity is pain. The duration of abscesses takes days to weeks
Ariana Kupai et al.
Frontiers in cell and developmental biology, 8, 241-241 (2020-04-25)
Lysine methylation facilitates protein-protein interactions through the activity of methyllysine (Kme) "reader" proteins. Functions of Kme readers have historically been studied in the context of histone interactions, where readers aid in chromatin-templated processes such as transcription, DNA replication and repair.
Alastair B Ross
Journal of agricultural and food chemistry, 60(36), 8954-8962 (2012-08-14)
Alkylresorcinols are phenolic lipids, with homologues ranging from C17 to C25, found in high concentrations in whole grain wheat and rye, lower concentrations in barley, and negligible concentrations in refined wheat flour. The analysis of alkylresorcinols is of importance due
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

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