CAS RN: 17305-22-5
(S)-(+)-3-METHYLPIPERIDINE
Product Availability
Choose a grade to view its available package options.
5 package records4 with current stock1 grade group
| Batch No. | Package | Availability | Warehouse | Lead Time | Inquiry |
|---|---|---|---|---|---|
| Batchno.20260406 | 100mg | In stock | Shanghai, Shenzhen, Chengdu | Inquiry | |
| Batchno.20260414 | 100mg / 250mg / 1g / 5g | Out of stock | 5-7 business days | Inquiry | |
| Batchno.20260606 | 1g | In stock | Shanghai | Inquiry | |
| Batchno.20250414 | 250mg | In stock | Shanghai | Inquiry | |
| Batchno.20251114 | 5g | In stock | Shenzhen, Chengdu | Inquiry |
- Product code: SSC-076023
Verified Factory Data
Supply Overview & Packaging Options
Packaging options, recorded purity, stock quantity and ship-from location below are generated from the current factory data table for this CAS.
- Pack sizes on record: 0.1g, 0.25g, 1g, 5g
- Available purity: >97%
- Inventory rows with stock: 4
- Bulk packaging: confirmed by inquiry
Available Pack Sizes & Stock
Specific stock quantities are shown below. Price is not displayed online and is confirmed by inquiry.
17305-22-5 / (3S)-3-methylpiperidine
Basic Information
CAS
17305-22-5
Multi CAS
No
Molecular Formula
C6H13N
Molecular Weight
99.170000
Exact Mass
99.104799
SMILES
C[C@H]1CCCNC1
InChI
InChI=1S/C6H13N/c1-6-3-2-4-7-5-6/h6-7H,2-5H2,1H3/t6-/m0/s1
InChIKey
JEGMWWXJUXDNJN-LURJTMIESA-N
Computed Properties
Structural Parameters
Heavy atom count
7
Fraction Csp3
1
H-bond acceptors
1
H-bond donors
1
Molar refractivity
31.27
TPSA
12.03
LogP / Solubility
WLOGP
1.01
MLOGP
0.87
XLogP3
1.1
Consensus LogP
0.99
Log S (ESOL)
-1.09
Class (ESOL)
Soluble
Log S (Ali)
-1.1
Class (Ali)
Soluble
Log S (SILICOS-IT)
-1.14
Class (SILICOS-IT)
Soluble
ADME
GI absorption
High
BBB permeant
Yes
P-gp substrate
No
CYP1A2 inhibitor
No
CYP2C19 inhibitor
No
CYP2C9 inhibitor
No
CYP2D6 inhibitor
No
CYP3A4 inhibitor
No
Log Kp (skin permeation)
-2.61
Drug-likeness / Medicinal Chemistry
Lipinski
Yes
Ghose
No
Veber
Yes
Egan
Yes
Muegge
No
Bioavailability score
0.55
Leadlikeness
No
Synthetic Accessibility
2
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