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628-13-7 molecular structure
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pyridine hydrochloride

ChemBase ID: 76878
Molecular Formular: C5H6ClN
Molecular Mass: 115.56084
Monoisotopic Mass: 115.01887688
SMILES and InChIs

SMILES:
n1ccccc1.Cl
Canonical SMILES:
c1cccnc1.Cl
InChI:
InChI=1S/C5H5N.ClH/c1-2-4-6-5-3-1;/h1-5H;1H
InChIKey:
AOJFQRQNPXYVLM-UHFFFAOYSA-N

Cite this record

CBID:76878 http://www.chembase.cn/molecule-76878.html

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NAMES AND DATABASE IDS

NAMES AND DATABASE IDS

Names Database IDs
IUPAC name
pyridine hydrochloride
IUPAC Traditional name
pyridine hydrochloride
Synonyms
Pyridine hydrochloride
PYRIDINE HYDROCHLORIDE TECHNICAL GRADE
Pyridinium chloride
Pyridine hydrochloride
吡啶盐酸盐
吡啶盐酸盐
吡啶 盐酸盐
CAS Number
628-13-7
EC Number
211-027-4
MDL Number
MFCD00012802
Beilstein Number
3615340
PubChem SID
24888045
24854598
162041780
PubChem CID
10176127

CALCULATED PROPERTIES

CALCULATED PROPERTIES

JChem
H Acceptors H Donor
LogD (pH = 5.5) 0.6230428  LogD (pH = 7.4) 0.75354445 
Log P 0.7555734  Molar Refractivity 23.9011 cm3
Polarizability 9.4423685 Å3 Polar Surface Area 12.89 Å2
Rotatable Bonds Lipinski's Rule of Five true 

PROPERTIES

PROPERTIES

Physical Property Safety Information Product Information Bioassay(PubChem)
Solubility
Methanol expand Show data source
Water expand Show data source
Apperance
White to Off-White Solid expand Show data source
Melting Point
138-142°C expand Show data source
143-147 °C expand Show data source
145-147 °C(lit.) expand Show data source
ca 145°C expand Show data source
Boiling Point
222-224 °C(lit.) expand Show data source
222-224°C expand Show data source
Storage Condition
Refrigerator expand Show data source
Storage Warning
Harmful/Hygroscopic expand Show data source
Hygroscopic expand Show data source
RTECS
UT4375000 expand Show data source
European Hazard Symbols
X expand Show data source
Harmful Harmful (Xn) expand Show data source
MSDS Link
Download expand Show data source
Download expand Show data source
Download expand Show data source
Download expand Show data source
German water hazard class
3 expand Show data source
Risk Statements
20/21/22-36/37/38 expand Show data source
22-36/37/38 expand Show data source
R:22 expand Show data source
Safety Statements
26-36 expand Show data source
26-36/37-60 expand Show data source
S:36/37/39 expand Show data source
TSCA Listed
expand Show data source
GHS Pictograms
GHS07 expand Show data source
GHS Signal Word
Warning expand Show data source
GHS Hazard statements
H302-H315-H319-H332-H335 expand Show data source
H302-H315-H319-H335 expand Show data source
GHS Precautionary statements
P261-P305 + P351 + P338 expand Show data source
P261-P305+P351+P338-P302+P352-P321-P405-P501A expand Show data source
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves expand Show data source
Purity
≥98.0% (AT) expand Show data source
98% expand Show data source
Grade
purum expand Show data source
TECHNICAL expand Show data source
Certificate of Analysis
Download expand Show data source
Download expand Show data source
Empirical Formula (Hill Notation)
C5H5N · HCl expand Show data source

DETAILS

DETAILS

MP Biomedicals MP Biomedicals Sigma Aldrich Sigma Aldrich TRC TRC
MP Biomedicals - 05217977 external link
MP Biomedicals Rare Chemical collection
Sigma Aldrich - 243086 external link
Packaging
100, 500 g in poly bottle
5 g in glass bottle
Toronto Research Chemicals - P991280 external link
Pyridine Hydrochloride is the hydrochloride salt of pyridine, a basic six-membered heterocyclic ring. Pyridine is a base structure present in many biologically active compounds like the vitamins niacin and pyridoxal. Pyridine is used in dehalogenation rea

REFERENCES

REFERENCES

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  • • Egyed, J. et al.: Bull. Soc. Chim. Fra., 11, 3014 (1973)
  • • Li, Y. et al.: Wuli HUa. Xueb., 14, 1048 (1973)
  • • Demethylation of methyl aryl ethers can also be carried out under solvent-free conditions with microwave irradiation: J. Chem. Res. (Synop.), 394 (1999).
  • • Epoxides at ambient temperature in chloroform give chlorohydrins: Synth. Commun., 11, 287 (1981).
  • • In DMF, has been used for the conversion of alkyl tosylates to chlorides at room temperature: J. Am. Chem. Soc., 80, 2726 (1958).
  • • Cleaves N-trityl groups from histidine residues in peptide synthesis: Tetrahedron Lett., 28, 6031 (1987).
  • • Classical reagent for cleavage of aryl methyl ethers at 200-220 o : Ber ., 75, 445 (1942), avoiding the strongly acidic or basic conditions of some alternative methods; see, e.g.: J. Org. Chem., 27, 4660 (1962):
  • • Mild acid catalyst, e.g. in the formation of acetals with ethylene glycol: J. Org. Chem., 31, 26 (1966), or 1,3-propanediol: Bull. Soc. Chim. Fr., 2287 (1972); and in the Fischer indole synthesis for acid-sensitive substrates: Synthesis, 645 (1977).
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PATENTS

PATENTS

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INTERNET

INTERNET

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