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General Material Information

Preferred name 2-pyridyl carbinol
Trivial Name 2-Pyridinemethanol
Short Description pyridine, 2-(hydroxymethyl)-
Formula C6 H7 N O
CAS Number 586-98-1
ECHA Number 209-592-7
FDA UNII 7HQ8UT1TPS
Nikkaji Number J32.889H
Beilstein Number 0107849
MDL MFCD00006348
Bio Activity Summary External link
NMR Predictor External link
Synonyms
  • 2-hydromethyl pyridine
  • 2-hydromethyl-pyridine
  • 2-hydroxymethyl pyridine
  • 2-hydroxymethyl-pyridine
  • 2-( hydroxymethyl)pyridine
  • 2-hydroxymethylpyridine
  • 2-picolyl alcohol
  • alpha- picolyl alcohol
  • piconol
  • ( pyridin-2-yl)methanol
  • pyridin-2-ylmethanol
  • pyridine-2-carbinol
  • pyridine-2-methanol
  • pyridine-2-ylmethanol
  • pyridine, 2-(hydroxymethyl)-
  • 2-pyridinemethanol
  • 2-pyridinyl methanol
  • 2-pyridinylmethanol
  • 2-pyridylcarbinol
  • 2-pyridylmethan-1-ol
  • 2-pyridylmethanol
  • 2-Pyridinemethanol
  • 2-(Hydroxymethyl)pyridine
  • 2-Pyridylcarbinol
  • 2-Pyridylmethanol
  • α-Picolyl alcohol
  • 2-Pyridinylmethanol
  • 2-Pyridinylcarbinol

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Literature & References

pyridin-2-ylmethanol
NIST Chemistry WebBook:Search Inchi
Pubchem (cid):11474
Pubchem (sid):134976166
Publications by US Patents
3,952,024 - Furfurylthioacetone
Certain 2,5-dimethyl-3-thiopyrazines
Publications by PubMed
A one-dimensional coordination polymer with a capped [Cu4O4] cubane core assembled from 2-(hydroxymethyl)pyridine.
Manganese/cerium clusters spanning a range of oxidation levels and CeMn(8), Ce(2)Mn(4), and Ce(6)Mn(4) nuclearities: structural, magnetic, and EPR properties.
A racemic and enantiopure unsymmetric diiron(III) complex with a chiral o-carborane-based pyridylalcohol ligand: combined chiroptical, magnetic, and nonlinear optical properties.
Closer to photosystem II: a Co4O4 cubane catalyst with flexible ligand architecture.
Synthesis, structural characterization and cell death-inducing effect of novel palladium(II) and platinum(II) saccharinate complexes with 2-(hydroxymethyl)pyridine and 2-(2-hydroxyethyl)pyridine on cancer cells in vitro.
Two novel lead(II) complexes of 2-(hydroxymethyl)pyridine: a threefold diamondoid supramolecular network based on Pb4O4 cores and a two-dimensional (4,4) network based on Pb2O2 units.
Synthesis, crystal structures, DNA binding and cytotoxicity of two novel platinum(II) complexes containing 2-(hydroxymethyl)pyridine and pyridine-2-carboxylate ligands.
trans-Dichloridopalladium(II) and platinum(II) complexes with 2-(hydroxymethyl)pyridine and 2-(2-hydroxyethyl)pyridine: synthesis, structural characterization, DNA binding and in vitro cytotoxicity studies.
Tuning the interactions from antiferro- to ferro-magnetic by molecular tailoring and manipulating.
Bis[2-(2-hy-droxy-meth-yl)pyridine-κ(2)N,O](pivalato-κO)copper(II).
Synthesis, structure and magnetic study of a novel mixed-valent Co(II)10Co(III)4 shield constructed by mixed pyridine-alcoholate ligands.
New mixed-valent Mn clusters from the use of N,N,N',N'-tetrakis(2-hydroxyethyl)ethylenediamine (edteH4): Mn3, Mn4, Mn6, and Mn10.
A new family of nonanuclear lanthanide clusters displaying magnetic and optical properties.
Carboxylate-free Mn(III)2Ln(III)2 (Ln = lanthanide) and Mn(III)2Y(III)2 complexes from the use of (2-hydroxymethyl)pyridine: analysis of spin frustration effects.
Mn8 and Mn16 clusters from the use of 2-(hydroxymethyl)pyridine, and comparison with the products from bulkier chelates: a new high nuclearity single-molecule magnet.
A linear tetranuclear single-molelcule magnet of Mn(II)(2)Mn(III)(2) with the anion of 2-(Hydroxymethyl)pyridine.
Mn(7) and Mn(12) clusters from use of 2-(pyridine-2-yl)propan-2-ol: a new half-integer single-molecule magnet.
Mn4, Mn6, and Mn11 clusters from the use of bulky diphenyl(pyridine-2-yl)methanol.
Azide groups in higher oxidation state manganese cluster chemistry: from structural aesthetics to single-molecule magnets.
High-spin Mn4 and Mn10 molecules: large spin changes with structure in mixed-valence MnII4MnIII6 clusters with azide and alkoxide-based ligands.
New Fe4, Fe6, and Fe8 clusters of iron(III) from the use of 2-pyridyl alcohols: structural, magnetic, and computational characterization.
Synthesis, structures, and magnetic properties of heteronuclear Cu(II)-Ln(III) (Ln = La, Gd, or Tb) complexes.
Synthesis, structure, and magnetic properties of a Mn(21) single-molecule magnet.
Heptanuclear and decanuclear manganese complexes with the anion of 2-hydroxymethylpyridine.
Single-molecule magnets: a new family of Mn(12) clusters of formula [Mn(12)O(8)X(4)(O(2)CPh)(8)L(6)].

Other Information

(IUPAC):Atomic Weights of the Elements 2011 (pdf)
Videos:The Periodic Table of Videos
tgsc:Atomic Weights use for this web site
(IUPAC):Periodic Table of the Elements
CHEMBL:View
HMDB (The Human Metabolome Database):Search
Export Tariff Code:2933.39.9100
ChemSpider:View

PhysChem Properties

Material listed in food chemical codex No
Molecular weight 109.12799072266
Specific gravity @ 20 °C
Pounds per Gallon 9.439 to 9.455
Refractive Index 1.542 to 1.546 @ 20 °C
Melting Point -6 to -5°C @ 760 mm Hg
Boiling Point 222 to 223°C @ 760 mm Hg
Vapor Pressure 0.026 mmHg @ 25 °C
Flash Point TCC Value 81.7 °C TCC
logP (o/w) 0.06
Solubility
water, 1e+006 mg/L @ 25 °C (est) Yes

Organoleptic Properties

Flavor Type: Roasted
roasted, moldy
General comment Roasted moldy

Safety Information

Safety information

Preferred SDS: View
Hazards identification
Classification of the substance or mixture
GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)
None found.
GHS Label elements, including precautionary statements
Pictogram
Hazard statement(s)
None found.
Precautionary statement(s)
None found.
Oral/Parenteral Toxicity:
oral-quail LD50 1000 mg/kg
Archives of Environmental Contamination and Toxicology. Vol. 12, Pg. 355, 1983.

intravenous-mouse LD50 1000 mg/kg
Pharmazie. Vol. 11, Pg. 242, 1956.

oral-bird - wild LD50 750 mg/kg
Archives of Environmental Contamination and Toxicology. Vol. 12, Pg. 355, 1983.

Dermal Toxicity:
Not determined
Inhalation Toxicity:
Not determined

Safety in use information

Category:
information only not used for fragrances or flavors
Recommendation for 2-pyridyl carbinol usage levels up to:
not for fragrance use.
Recommendation for 2-pyridyl carbinol flavor usage levels up to:
not for flavor use.

Safety references

EPI System: View
AIDS Citations:Search
Cancer Citations:Search
Toxicology Citations:Search
EPA ACToR:Toxicology Data
EPA Substance Registry Services (SRS):Registry
Laboratory Chemical Safety Summary :11474
National Institute of Allergy and Infectious Diseases:Data
WGK Germany:3
pyridin-2-ylmethanol
Chemidplus:0000586981
RTECS:UT4689000 for cas# 586-98-1