Clorhidrato de milnaciprán - ≥99% , CAS No.101152-94-7

CAS: 101152-94-7 Cat. No.: M129386 Peso molecular: 282.81 Número EC: 620-477-4
Disponible para pedir
GRADE & PURITY ≥99%
Synonyms
?4-DIMETHYLAMINO-4'-METHYLAZOBENZENE | Toledomin | CAS-3027-21-2 | 1 Phenyl 1 diethylaminocarbonyl 2 aminomethylcyclopropane HCl | CHEBI:31854 | DTXCID2026785 | BCP05817 | Cyclopropanecarboxamide, 2-(aminomethyl)-N,N-diethyl-1-phenyl-, monohydrochloride,
Storage
Conservar a 2-8°C
Shipped In
Hielo húmedo
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
10mg
M129386-10mg
3
10,90US$
50mg
M129386-50mg
3
21,90US$
250mg
M129386-250mg
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.
65,90US$
500mg
M129386-500mg
2
116,90US$
1g
M129386-1g
3
185,90US$
5g
M129386-5g
2
767,90US$
25g
M129386-25g
1
2.648,90US$
Enter a quantity for the sizes you want to add.
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Why this grade

≥99% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Conservar a 2-8°C Ships Hielo húmedo Check lot-specific COA for exact specifications.

📋

Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Descripción general

El milnaciprán inhibe tanto el transportador de norepinefrina (NET) como el transportador de norepinefrina (SERT) con IC50 de 77 nM y 420 nM, respectivamente.

Specifications

Sinónimos
?4-DIMETHYLAMINO-4'-METHYLAZOBENZENE | Toledomin | CAS-3027-21-2 | 1 Phenyl 1 diethylaminocarbonyl 2 aminomethylcyclopropane HCl | CHEBI:31854 | DTXCID2026785 | BCP05817 | Cyclopropanecarboxamide, 2-(aminomethyl)-N, N-diethyl-1-phenyl-, monohydrochloride,
Especificaciones y pureza
≥99%
Mecanismos bioquímicos y fisiológicos
El milnaciprán inhibe tanto el SLC6A2 (transportador de norepinefrina/NET) como el ST (transportador de norepinefrina/SERT) con IC50 de 77 nM y 420 nM, respectivamente.Inhibidor de la recaptación de serotonina y norepinefrina. Los valores de IC 50 son 100
Condiciones de almacenamiento de almacenamiento
Conservar a 2-8°C
Enviado en
Hielo húmedo
Nota
Siempre que sea posible, prepare y utilice las soluciones el mismo día. Sin embargo, si necesita preparar soluciones madre con antelación, le recomendamos que almacene la solución como alícuotas en viales herméticamente cerrados a -20°C. Por lo general, podrán utilizarse durante un mes. Antes de su uso, y antes de abrir el vial, le recomendamos que deje que el producto se equilibre a temperatura ambiente durante al menos 1 hora. Toxicidad, consulte la SDS para más información. ¿Necesita más consejos sobre solubilidad, uso y manipulación? Visite nuestra página de preguntas frecuentes (FAQ) para obtener más información.
Pureza
≥99%
Nombres e identificadores
Pubchem Sid504757538
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504757538
Sonrisas canónicasCCN(CC)C(=O)C1(CC1CN)C2=CC=CC=C2.Cl
IUPAC Name(1R,2S)-2-(aminomethyl)-N,N-diethyl-1-phenylcyclopropane-1-carboxamide;hydrochloride
InChIKeyXNCDYJFPRPDERF-PBCQUBLHSA-N
INCHI1S/C15H22N2O.ClH/c1-3-17(4-2)14(18)15(10-13(15)11-16)12-8-6-5-7-9-12;/h5-9,13H,3-4,10-11,16H2,1-2H3;1H/t13-,15+;/m1./s1
Isómeros SMILES CCN(CC)C(=O)[C@@]1(C[C@@H]1CN)C2=CC=CC=C2.Cl
WGK Alemania 3
RTECS GZ1014010
Número ONU 2811
Grupo de embalaje III
Peso molecular 282.81
Reaxy-Rn 11213530
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=11213530&ln=

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassBenzenoids
ClaseBenzene and substituted derivatives
SubclassPhenylacetamides
Intermediate Tree Nodes Not available
Direct ParentPhenylacetamides
Alternative Parents Aralkylamines  Cyclopropanecarboxylic acids and derivatives  Tertiary carboxylic acid amides  Amino acids and derivatives  Organopnictogen compounds  Organic oxides  Organic chloride salts  Monoalkylamines  Hydrocarbon derivatives  Carbonyl compounds  
Molecular FrameworkAromatic homomonocyclic compounds
Substituents Phenylacetamide - Aralkylamine - Cyclopropanecarboxylic acid or derivatives - Tertiary carboxylic acid amide - Amino acid or derivatives - Carboxamide group - Carboxylic acid derivative - Amine - Organic salt - Organic chloride salt - Hydrocarbon derivative - Primary amine - Organooxygen compound - Organonitrogen compound - Primary aliphatic amine - Organic oxide - Organopnictogen compound - Organic oxygen compound - Carbonyl group - Organic nitrogen compound - Aromatic homomonocyclic compound
DescripciónThis compound belongs to the class of organic compounds known as phenylacetamides. These are amide derivatives of phenylacetic acids.
External Descriptors Not available
Estructura 3D
Modelo de Estructura Química Interactiva





Objetivos asociados (humanos)
SLC6A2 Tclin Norepinephrine transporter (10102 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
KDM4E Tchem Lysine-specific demethylase 4D-like (40243 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Objetivos asociados (no humanos)
Mapk1 MAP kinase ERK2 (650 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Pseudomonas aeruginosa (123386 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Klebsiella pneumoniae (43867 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Staphylococcus aureus (210822 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Acinetobacter baumannii (41033 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Escherichia coli (133304 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Cryptococcus neoformans (21258 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Candida albicans (78123 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mus musculus (284745 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mecanismos de acción
Certificados (CoA, COO, BSE/TSE y tabla de análisis)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

5 results found

Lot NumberCertificate TypeFechaArticulo
D1924114Certificate of AnalysisMay 21, 2026 M129386
C2208472Certificate of AnalysisSep 09, 2025 M129386
C2208473Certificate of AnalysisSep 09, 2025 M129386
C2208491Certificate of AnalysisSep 09, 2025 M129386
G1529057Certificate of AnalysisNov 15, 2024 M129386
Propiedades químicas y físicas
SolubilidadDMSO 57 mg/mL Water 57 mg/mL Ethanol 57 mg/mL
SensibilidadHeat sensitive
Punto de fusión (°C)181°C(dec.)(lit.)
Peso molecular282.810 g/mol
XLogP3
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count2
Rotatable Bond Count5
Exact Mass282.15 Da
Monoisotopic Mass282.15 Da
Topological Polar Surface Area46.300 Ų
Heavy Atom Count19
Formal Charge0
Complexity295.000
Isotope Atom Count0
Defined Atom Stereocenter Count2
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count2
Calculadoras de soluciones
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