EU/US Properties Organoleptics Cosmetics Suppliers Safety Safety in use Safety references References Other Blenders Uses Occurrence Synonyms Articles Notes


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CAS Number: 586-95-8Picture of molecule3D/inchi
ECHA EINECS - REACH Pre-Reg:209-590-6
FDA UNII: Search
Nikkaji Web:J85.689D
Beilstein Number:107850
XlogP3:0.10 (est)
Molecular Weight:109.12799000
Formula:C6 H7 N O
BioActivity Summary:listing
NMR Predictor:Predict (works with chrome, Edge or firefox)
Category:information only not used for fragrances or flavors
US / EU / FDA / JECFA / FEMA / FLAVIS / Scholar / Patent Information:
Google Scholar:Search
Google Books:Search
Google Scholar: with word "volatile"Search
Google Scholar: with word "flavor"Search
Google Scholar: with word "odor"Search
Google Patents:Search
US Patents:Search
EU Patents:Search
Pubchem Patents:Search
Physical Properties:
Assay: 95.00 to 100.00
Food Chemicals Codex Listed: No
Melting Point: 53.00 °C. @ 760.00 mm Hg
Vapor Pressure:0.026000 mmHg @ 20.00 °C.
Flash Point:> 230.00 °F. TCC ( > 110.00 °C. )
logP (o/w): 0.060
Soluble in:
 water, 1.00E+06 mg/L @ 20 °C (exp)
Organoleptic Properties:
Flavor Type: hazelnut
hazelnut coffee nutty
Taste Description: hazelnut- coffee-like
Odor and/or flavor descriptions from others (if found).
Cosmetic Information:
None found
BOC Sciences
For experimental / research use only.
4-Hydroxymethylpyridine 98%
Glentham Life Sciences
Matrix Scientific
For experimental / research use only.
Pyridine-4-methanol, 98%
Santa Cruz Biotechnology
For experimental / research use only.
Sigma-Aldrich: Aldrich
For experimental / research use only.
4-Pyridinemethanol 99%
For experimental / research use only.
4-Pyridinemethanol >97.0%(GC)
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
Hazard statement(s)
None found.
Precautionary statement(s)
None found.
Oral/Parenteral Toxicity:
oral-bird - wild LD50 422 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.

Dermal Toxicity:
Not determined
Inhalation Toxicity:
Not determined
Safety in Use Information:
information only not used for fragrances or flavors
Recommendation for 4-hydroxymethyl-pyridine usage levels up to:
 not for fragrance use.
Recommendation for 4-hydroxymethyl-pyridine flavor usage levels up to:
 not for flavor use.
Safety References:
EPI System: View
AIDS Citations:Search
Cancer Citations:Search
Toxicology Citations:Search
EPA Substance Registry Services (TSCA):586-95-8
EPA ACToR:Toxicology Data
EPA Substance Registry Services (SRS):Registry
Laboratory Chemical Safety Summary :11472
National Institute of Allergy and Infectious Diseases:Data
WGK Germany:3
RTECS:UT4691000 for cas# 586-95-8
NIST Chemistry WebBook:Search Inchi
Pubchem (cid):11472
Pubchem (sid):134975976
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
HMDB (The Human Metabolome Database):Search
Export Tariff Code:2933.39.9100
Potential Blenders and core components note
None Found
Potential Uses:
None Found
Occurrence (nature, food, other):note
 not found in nature
4-hydroxymethyl pyridine
4-picolyl alcohol
gamma-picolyl alcohol
4-pyridyl carbinol


US Patents:3,952,024 - Furfurylthioacetone
PubMed:The role of p53 in the cellular toxicity by active trans-platinum complexes containing isopropylamine and hydroxymethylpyridine.
US Patents:Certain 2,5-dimethyl-3-thiopyrazines
PubMed:Study by HPLC-MS of the interaction of platinum antitumor complexes with potato carboxypeptidase inhibitor (PCI).
PubMed:Influence of the position of substituents in the cytotoxic activity of trans platinum complexes with hydroxymethyl pyridines.
PubMed:Selective intracellular accumulation of the major metabolite issued from the activation of the prodrug ethionamide in mycobacteria.
PubMed:Chelation-assisted transformation: synthesis of 1,4-dicarboxylate esters by the Rh-catalyzed carbonylation of internal alkynes with pyridin-2-ylmethanol.
PubMed:Synthesis and anti-HIV-1 and anti-HCMV activity of 1-substituted 3-(3,5-dimethylbenzyl)uracil derivatives.
PubMed:Recognition of DNA modified by trans-[PtClNH(4-hydroxymethylpyridine)] by tumor suppressor protein p53 and character of DNA adducts of this cytotoxic complex.
PubMed:Synthesis, characterization and biological activity of trans-platinum(II) and trans-platinum(IV) complexes with 4-hydroxymethylpyridine.
PubMed:The thermal and light induced spin transition in [FeL2](BF4)2 (L = 2,6-dipyrazol-1-yl-4-hydroxymethylpyridine).
PubMed:On the formation of isopropylidenepyridoxines. A convenient method for the preparation of 2,2,8-trimethyl-4H-1,3-dioxino[4,5-c]pyridin-5-ylmethanol from pyridoxine hydrochloride.
PubMed:[Pharmacodynamic study of (M-14012-4) N-(4-picolyl)-3,5-dimethylbenzamide].
None found
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