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Safety Information

385646

Sigma-Aldrich

4-Pyridinepropanol

96%

Synonym(s):

3-(4-Pyridyl)-1-propanol

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About This Item

Empirical Formula (Hill Notation):
C8H11NO
CAS Number:
2629-72-3
Molecular Weight:
137.18
EC Number:
220-107-8
MDL number:
MFCD00047457
UNSPSC Code:
12352100
PubChem Substance ID:
24864041
NACRES:
NA.22

Quality Level

200

Assay

96%

bp

289 °C (lit.)

mp

35-39 °C (lit.)

density

1.061 g/mL at 25 °C (lit.)

functional group

hydroxyl

SMILES string

OCCCc1ccncc1

InChI

1S/C8H11NO/c10-7-1-2-8-3-5-9-6-4-8/h3-6,10H,1-2,7H2

InChI key

PZVZGDBCMQBRMA-UHFFFAOYSA-N

Application

Used to construct a linear axle containing perfluoro stoppers in the synthesis of a rotaxane from dibenzo-24-crown-8.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Precautionary Statements

P261 - P305 + P351 + P338

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

235.4 °F - closed cup

Flash Point(C)

113 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

385646-VAR:
385646-BULK:
385646-100G:
385646-500G:

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Certificates of Analysis (COA)

Lot/Batch Number
MKAA0042
03622BJ
05704AH
12728TD
08604PD

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Jin Matsumoto et al.
Journal of photochemistry and photobiology. B, Biology, 168, 124-131 (2017-02-20)
Activity of singlet oxygen sensitizers for photoinactivation of bacteria and photodynamic therapy of tumor cells has been evaluated using nonpathogenic model cells, such as Escherichia coli, Saccharomyces cerevisiae, and HeLa cells. Among them, E. coli, gram-negative bacterium, has complex membrane
Eric J Mahan et al.
Organic letters, 8(22), 5085-5088 (2006-10-20)
A novel [2]-rotaxane has been prepared in which perfluoropropyl stoppers have been utilized as electronic blocking groups. To further investigate this capability, a linear compound that was precapped with perfluoropropyl groups was also prepared. This compound did not demonstrate rotaxane

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