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V209

δ-Valerolactam

98%

Synonym(s):

delta-Valerolactam, 2-Piperidone

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25 g

Estimated to ship TODAYfromMILWAUKEE

$88.60
100 g
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$233.00

About This Item

Empirical Formula (Hill Notation):
C5H9NO
CAS Number:
675-20-7
Molecular Weight:
99.13
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24900726
EC Number:
211-622-9
Beilstein/REAXYS Number:
106434
MDL number:
MFCD00006037
Assay:
98%

$88.60

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Quality Level

200

assay

98%

bp

256 °C (lit.), 81-82 °C/0.1 mmHg (lit.)

mp

38-40 °C (lit.)

SMILES string

O=C1CCCCN1

InChI

1S/C5H9NO/c7-5-3-1-2-4-6-5/h1-4H2,(H,6,7)

InChI key

XUWHAWMETYGRKB-UHFFFAOYSA-N

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This Item
W316700F0120010W329415
δ-Valerolactam 98%

Sigma-Aldrich

V209

δ-Valerolactam

δ-Hexalactone ≥98%, FG

Sigma-Aldrich

W316700

δ-Hexalactone

Flecainide impurity B European Pharmacopoeia (EP) Reference Standard

F0120010

Flecainide impurity B

δ-Undecalactone, mixture of isomers natural, 98%, FG

Sigma-Aldrich

W329415

δ-Undecalactone, mixture of isomers

assay

98%

assay

≥98%

assay

-

assay

98%

Quality Level

200

Quality Level

300

Quality Level

-

Quality Level

300

mp

38-40 °C (lit.)

mp

-

mp

-

mp

-

bp

256 °C (lit.), 81-82 °C/0.1 mmHg (lit.)

bp

110-112 °C/15 mmHg (lit.)

bp

-

bp

152-155 °C/10.5 mmHg (lit.)

pictograms

Exclamation mark
GHS07

signalword

Warning

hcodes

H319

Hazard Classifications

Eye Irrit. 2

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

235.4 °F - closed cup

flash_point_c

113 °C - closed cup

ppe

Eyeshields, Gloves, type N95 (US)

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Certificates of Analysis (COA)

Lot/Batch Number
SDBB1315
STBK7787
STBK4280
STBK0477
STBJ4074

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Haili Lin et al.
Experimental & molecular medicine, 52(3), 367-379 (2020-03-11)
The function of the fibrinolytic system was first identified to dissolve fibrin to maintain vascular patency. Connections between the fibrinolytic system and many other physiological and pathological processes have been well established. Dysregulation of the fibrinolytic system is closely associated
Mitchell G Thompson et al.
ACS synthetic biology, 9(1), 53-62 (2019-12-17)
Caprolactam is an important polymer precursor to nylon traditionally derived from petroleum and produced on a scale of 5 million tons per year. Current biological pathways for the production of caprolactam are inefficient with titers not exceeding 2 mg/L, necessitating
Tong Un Chae et al.
Metabolic engineering, 41, 82-91 (2017-04-10)
Microbial production of chemicals and materials from renewable sources is becoming increasingly important for sustainable chemical industry. Here, we report construction of a new and efficient platform metabolic pathway for the production of four-carbon (butyrolactam), five-carbon (valerolactam) and six-carbon (caprolactam)
Moitrayee Mukherjee et al.
The journal of physical chemistry. A, 116(40), 9888-9896 (2012-09-19)
A comparative analysis for relative stability between normal and tautomeric forms in the excited electronic states of 7-azaindole···δ-valerolactam 1:1 complex and 7-azaindole homodimer has been presented. The tautomeric configuration of the complex is estimated to be ~6 kcal/mol more stable
Ahmed Mahjoub et al.
Chemphyschem : a European journal of chemical physics and physical chemistry, 12(10), 1822-1832 (2011-05-28)
We studied the single-photon ionization of gas-phase δ-valerolactam (piperidin-2-one) and of its dimer using vacuum-ultraviolet (VUV) synchrotron radiation coupled to a velocity map imaging electron/ion coincidence spectrometer. The slow photoelectron spectrum (SPES) of the monomer is dominated by the vibrational
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Global Trade Item Number

SKUGTIN
V209-25G04061837480744
V209-100G04061837480737

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