Home Pyridines 100-55-0
100-55-0,MFCD00006407
Catalog No.:AA00004J
100-55-0 | 3-Pyridinemethanol
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5g
98%
in stock  
$9.00   $7.00
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10g
98%
in stock  
$14.00   $10.00
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25g
98%
in stock  
$17.00   $12.00
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100g
98%
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$45.00   $32.00
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500g
98%
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$220.00   $154.00
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  • Technical Information
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Technical Information
Catalog Number:
AA00004J
Chemical Name:
3-Pyridinemethanol
CAS Number:
100-55-0
Molecular Formula:
C6H7NO
Molecular Weight:
109.1259
MDL Number:
MFCD00006407
IUPAC Name:
pyridin-3-ylmethanol
InChI:
InChI=1S/C6H7NO/c8-5-6-2-1-3-7-4-6/h1-4,8H,5H2
InChI Key:
MVQVNTPHUGQQHK-UHFFFAOYSA-N
SMILES:
OCc1cccnc1
EC Number:
202-864-6
UNII:
9TF312056Y
NSC Number:
526046
Properties
Computed Properties
 
Complexity:
65.5  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
109.053g/mol
Formal Charge:
0
Heavy Atom Count:
8  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
1  
Isotope Atom Count:
0
Molecular Weight:
109.128g/mol
Monoisotopic Mass:
109.053g/mol
Rotatable Bond Count:
1  
Topological Polar Surface Area:
33.1A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
0

Synonyms
 
3 Hydroxymethylpyridine 
3-Hydroxymethylpyridine 
Nicotinyltartrate 
Jsp000140 
CHEMBL1235535 
DTXSID6023367 
BDBM92860 
CHEBI:45213 
CTK0H5236 
HMS2052G07 
HMS2232J07 
HMS3372K15 
HMS3394G07 
Pyridine 3 Methanol 
BCP20084 
HY-B0893 
Nicotinyl Alcohol (Pyridylcarbinol) 
STR00172 
Tox21_113448 
Tox21_300839 
ANW-14316 
Ro-15155 
SBB004344 
AKOS000119474 
Pyridine-3-Methanol 
Tox21_113448_1 
3-Pyridinemethanol, analytical standard 
CCG-101090 
CS-4356 
DB04145 
FG-0435 
MCULE-4350730997 
NC00340 
NSC-526046 
QC-4379 
Pyridylcarbinol 
RP00469 
VZ27242 
NCGC00159400-02 
NCGC00159400-03 
NCGC00159400-04 
NCGC00159400-06 
NCGC00159400-07 
NCGC00257521-01 
AC-15599 
AJ-08096 
Radecol 
AK-46173 
AM802808 
AN-25309 
BC209311 
CJ-00065 
CPD000059086 
FS011361 
HC150097 
SAM001246894 
SC-17825 
Roniacol 
ST075169 
SY001086 
ZB000415 
SBI-0052904.P002 
DB-012725 
LS-131670 
LS-131710 
ST2410844 
TC-063624 
FT-0083027 
Ronicol 
P0555 
KS-00000814 
MFCD00006407 (98%) 
D05158 
M-6218 
28068-EP2272841A1 
28068-EP2301936A1 
28068-EP2314588A1 
AB00053787_07 
3-Pyridinemethanol, Vetec(TM) reagent grade, 98% 
Ronicol Retard 
I02-0327 
J-650089 
W-108954 
F0001-0022 
InChI=1/C6H7NO/c8-5-6-2-1-3-7-4-6/h1-4,8H,5H 
Ronicol 
Radecol 
Ronicol retard 
|A pyridylcarbinol 
Alcohol, Nicotinic 
3-PYRIDINEMETHANOL 
Alcohol, Nicotinyl 
beta Pyridylcarbinol 
3-Piperidinemethanol 
Pyridine 3 Methanol 
C(O)c1cccnc1 
3-Piperidine Methanol 
3 Hydroxymethylpyridine 
Nicotinyl alcohol tartrate 
?-Hydroxy-3-picoline 
Hydrofluoride, Nicomethanol 
100-55-0 
C6-H7-N-O 
CID7510 
3-(Hydroxymethyl)pyridine oxalate hydrate 
3-Pyridinemethanol, 98% - 100G 100g 
D009540 
3-Pyridinemethanol, ethanedioate (1:1) (salt), hydrate 
4606-65-9 
PYF 
Alcohol, Nicotinic 
Nicotinyl alcohol 
pyridin-3-ylmethanol 
3-(Hydroxymethyl)pyridine 
3-Pyridylmethanol 
Nicotinic alcohol 
3-Pyridylcarbinol 
Roniacol 
3-Pyridinylmethanol 
Pyridylcarbinol 
Pyridine-3-carbinol 
Alcohol, Nicotinyl 
Pyridine-3-methanol 
beta-Pyridylcarbinol 
(Pyridin-3-yl)methanol 
3-Picolyl alcohol 
beta-Picolyl alcohol 
beta-Pyridinecarbinol 
Pyridylmethanol 
NU-2121 
Ro-1-5155 
3-PYRIDINYLCARBINOL 
beta Pyridylcarbinol 
Pyridyl-3-carbinol 
Pyridyl-3-methanol 
Niltuvin (free base) 
.beta.-Pyridylcarbinol 
3-Hydroxymethylpyridine 
Pyridin-3-Yl-Methanol 
.beta.-Picolyl alcohol 
.beta.-Pyridinecarbinol 
3-Pyridyl carbinol 
NSC 526046 
beta-Pyridylcarbinol 
Nicotinyl alcohol [USAN:BAN] 
UNII-9TF312056Y 
3-pyridylmethan-1-ol 
EINECS 202-864-6 
MFCD00006407 
C6H7NO 
BRN 0107851 
RO 1-5155 
Nicomethanol Hydrofluoride 
MVQVNTPHUGQQHK-UHFFFAOYSA-N 
Hydrofluoride, Nicomethanol 
NSC526046 
9TF312056Y 
NU 2121 
NCGC00159400-05 
Pyridine-3-methanol (3-Pyridylcarbinol) 
DSSTox_CID_3367 
DSSTox_RID_76995 
DSSTox_GSID_23367 
3-(Hydroxymethyl)pyridine, 98% 
Nicotinyltartrate 
Nicomethanol Hydrofluoride 
CAS-100-55-0 
SMR000059086 
3-Pyridinemthanol 
3-pyridyl methanol 
3-pyridyl-carbinol 
Roniacol (TN) 
3-pyridine methanol 
pyridine 3-methanol 
3-pyridinyl carbinol 
PncA Inhibitor, 4 
Nicotinic Alcohol 
Ronicol (Salt/Mix) 
pyridin-3-yl methanol 
3-pyridylmethyl alcohol 
PubChem11736 
3-hydroxymethyl pyridine 
3-hydroxymethyl-pyridine 
AC1L1OXA 
omega-Hydroxy-3-picoline 
ACMC-1C7ZK 
Nicotinyl alcohol (USAN) 
Nicotinyl Alcohol 
(3-Pyridyl)methyl alcohol 
3-Pyridinemethanol, 98% 
3-(hydroxymethyl)-pyridine 
AC1Q7C2F 
SCHEMBL16266 
5-21-02-00172 (Beilstein Handbook Reference) 
MLS000028906 
MLS001424215 
SCHEMBL9853210 
ZINC1799 
Literature

Title: Copper (II) complexes of the anti-inflammatory drug naproxen and 3-pyridylmethanol as auxiliary ligand. Characterization, superoxide dismutase and catecholase--mimetic activities.

Journal: European journal of medicinal chemistry 20100901

Title: Noncovalent synthesis of hierarchical zinc phosphates from a single Zn(4)O(12)P(4) double-four-ring building block: dimensionality control through the choice of auxiliary ligands.

Journal: Chemistry (Weinheim an der Bergstrasse, Germany) 20100118

Title: The role of p53 in the cellular toxicity by active trans-platinum complexes containing isopropylamine and hydroxymethylpyridine.

Journal: European journal of medicinal chemistry 20100101

Title: Synthesis and Structural Characterization of a Metal Cluster and a Coordination Polymer Based on the [Mn(6)(mu(4)-O)(2)] Unit.

Journal: Bioinorganic chemistry and applications 20100101

Title: Development of molecularly imprinted polymers as tailored templates for the solid-state [2+2] photodimerization.

Journal: Biosensors & bioelectronics 20091115

Title: Oxidation of alcohols using a manganese (II) complex based on a pentakis benzimidazole amide ligand.

Journal: Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy 20091001

Title: Characterization of a rat NADPH-dependent aldo-keto reductase (AKR1B13) induced by oxidative stress.

Journal: Chemico-biological interactions 20090316

Title: A rapid and sensitive method for the simultaneous analysis of aliphatic and polar molecules containing free carboxyl groups in plant extracts by LC-MS/MS.

Journal: Plant methods 20090101

Title: Equilibria of 3-pyridylmethanol with copper(II). A comparative electron spin resonance study by the decomposition of spectra in liquid and frozen solutions.

Journal: The journal of physical chemistry. A 20081016

Title: Improved synthesis of histone deacetylase inhibitors (HDIs) (MS-275 and CI-994) and inhibitory effects of HDIs alone or in combination with RAMBAs or retinoids on growth of human LNCaP prostate cancer cells and tumor xenografts.

Journal: Bioorganic & medicinal chemistry 20080315

Title: catena-Poly[[bis-[2-(2,3-dimethyl-anilino)benzoato-κO]cadmium(II)]-di-μ-3-pyridylmethanol-κN:O;κO:N].

Journal: Acta crystallographica. Section E, Structure reports online 20080301

Title: Enzymatic oxidation of NADP+ to its 4-oxo derivative is a side-reaction displayed only by the adrenodoxin reductase type of ferredoxin-NADP+ reductases.

Journal: The FEBS journal 20070801

Title: catena-Poly[[tetrakis(mu-propionato-kappa(2)O:O')dicopper(II)]-mu-3-pyridylmethanol-kappa(2)N:O-[bis(propionato-kappaO)bis(3-pyridylmethanol-kappaN)copper(II)]-mu-3-pyridylmethanol-kappaO:N].

Journal: Acta crystallographica. Section C, Crystal structure communications 20070301

Title: Picolinyl ester fragmentation mechanism studies with application to the identification of acylcarnitine acyl groups following transesterification.

Journal: Journal of the American Society for Mass Spectrometry 20061101

Title: Reaction of the tobacco alkaloid myosmine with hydrogen peroxide.

Journal: Chemical research in toxicology 20060101

Title: Metabolism of myosmine in Wistar rats.

Journal: Drug metabolism and disposition: the biological fate of chemicals 20051101

Title: Importance of free fatty acids as a determinant of myocardial oxygen consumption and myocardial ischemic injury during norepinephrine infusion in dogs.

Journal: The Journal of clinical investigation 19740501

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