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1-Naphthylamine - Analytical Reagent,99.0%, high purity , CAS No.134-32-7

    Grade & Purity:
  • AR
  • ≥99%
In stock
Item Number
N103784
Grouped product items
SKU Size
Availability
Price Qty
N103784-25g
25g
9
$41.90
N103784-100g
100g
2
$150.90
N103784-250g
250g
1
$338.90
N103784-500g
500g
1
$609.90

Basic Description

Synonyms BRN 0386133 | 1-naphthyl amine | alpha-Naftalamin | RCRA waste no. U167 | 1-amino napthalene | 1-Naftilamina | 1-Naphthylamin [German] | CI Azoic Diazo Component 114 | STK301604 | 1-Aminonaftalen [Czech] | 1-Naftylamin [Czech] | 1-Naphthylamine, analytica
Specifications & Purity AR, ≥99%
Storage Temp Store at 2-8°C,Argon charged
Shipped In
Wet ice
This product requires cold chain shipping. Ground and other economy services are not available.
Grade AR
Product Description

1-Naphthylamine has been used in the synthesis of Pitnot-2, an inactive analog of clathrin inhibitor Pitstop 2.

It can also be used as a starting material to synthesize:

· [(S)-HY-Phos], a novel chiral phosphine-phosphoramidite ligand for use in rhodium-catalyzed asymmetric hydrogenation of various functionalized olefins.

· N-(naphthalen-1-yl)picolinamide.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Benzenoids
Class Naphthalenes
Subclass Not available
Intermediate Tree Nodes Not available
Direct Parent Naphthalenes
Alternative Parents Primary amines  Organopnictogen compounds  Hydrocarbon derivatives  
Molecular Framework Aromatic homopolycyclic compounds
Substituents Naphthalene - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Primary amine - Organonitrogen compound - Amine - Aromatic homopolycyclic compound
Description This compound belongs to the class of organic compounds known as naphthalenes. These are compounds containing a naphthalene moiety, which consists of two fused benzene rings.
External Descriptors naphthylamine

Associated Targets(Human)

TSHR Tclin Thyroid stimulating hormone receptor (29986 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
AHR Tclin Aryl hydrocarbon receptor (1071 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
ALB Tchem Serum albumin (2651 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
ALDH1A1 Tchem Aldehyde dehydrogenase 1A1 (77053 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
UGT1A4 Tbio UDP-glucuronosyltransferase 1A4 (288 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
CYP3A4 Tclin Cytochrome P450 3A4 (53859 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
NCI-H1299 (3248 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Lymphoblastoid cell (5959 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
HSD17B10 Tchem Endoplasmic reticulum-associated amyloid beta-peptide-binding protein (20669 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
APEX1 Tchem DNA-(apurinic or apyrimidinic site) lyase (38016 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
UGT2B15 Tbio UDP-glucuronosyltransferase 2B15 (172 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
UGT1A1 Tchem UDP-glucuronosyltransferase 1-1 (448 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
HPGD Tchem 15-hydroxyprostaglandin dehydrogenase [NAD+] (24926 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
UGT1A6 Tbio UDP-glucuronosyltransferase 1-6 (221 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
UGT1A7 Tbio UDP-glucuronosyltransferase 1-7 (106 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
UGT1A9 Tbio UDP-glucuronosyltransferase 1-9 (343 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
UGT1A10 Tbio UDP-glucuronosyltransferase 1-10 (257 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
UGT2A1 UDP-glucuronosyltransferase 2A1 (59 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
KAT8 Tchem Histone acetyltransferase KAT8 (178 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
KEAP1 Tclin Kelch-like ECH-associated protein 1 (1736 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Associated Targets(non-human)

Abcb1b P-glycoprotein 1 (174 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Polycyclic aromatic hydrocarbon binding protein (16 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Nfe2l2 Nuclear factor erythroid 2-related factor 2 (214 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Mechanisms of Action

Mechanism of Action Action Type target ID Target Name Target Type Target Organism Binding Site Name References

Names and Identifiers

Pubchem Sid 504751709
Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/504751709
IUPAC Name naphthalen-1-amine
INCHI InChI=1S/C10H9N/c11-10-7-3-5-8-4-1-2-6-9(8)10/h1-7H,11H2
InChIKey RUFPHBVGCFYCNW-UHFFFAOYSA-N
Smiles C1=CC=C2C(=C1)C=CC=C2N
Isomeric SMILES C1=CC=C2C(=C1)C=CC=C2N
WGK Germany 2
RTECS QM1400000
UN Number 2077
Packing Group III
Molecular Weight 143.19
Beilstein 386133
Reaxy-Rn 386133
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=386133&ln=

Certificates(CoA,COO,BSE/TSE and Analysis Chart)

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.

26 results found

Lot Number Certificate Type Date Item
F2121245 Certificate of Analysis Apr 03, 2025 N103784
B2517338 Certificate of Analysis Jan 04, 2025 N103784
A2514584 Certificate of Analysis Jan 04, 2025 N103784
B2508462 Certificate of Analysis Jan 04, 2025 N103784
B2508470 Certificate of Analysis Jan 04, 2025 N103784
D2524064 Certificate of Analysis Jan 04, 2025 N103784
G2422108 Certificate of Analysis Jul 24, 2024 N103784
B2307750 Certificate of Analysis Dec 30, 2022 N103784
B2307720 Certificate of Analysis Dec 30, 2022 N103784
B2307826 Certificate of Analysis Dec 30, 2022 N103784
B2307704 Certificate of Analysis Dec 30, 2022 N103784
H2301179 Certificate of Analysis Dec 30, 2022 N103784
B2307880 Certificate of Analysis Dec 30, 2022 N103784
B2307746 Certificate of Analysis Dec 30, 2022 N103784
K2216293 Certificate of Analysis Nov 21, 2022 N103784
I2224572 Certificate of Analysis Jun 18, 2022 N103784
I2224574 Certificate of Analysis Jun 18, 2022 N103784
J2312052 Certificate of Analysis Jun 18, 2022 N103784
I2224575 Certificate of Analysis Jun 18, 2022 N103784
I2224573 Certificate of Analysis Jun 18, 2022 N103784
I2224570 Certificate of Analysis Jun 18, 2022 N103784
F2202290 Certificate of Analysis Jun 07, 2022 N103784
H2301103 Certificate of Analysis Jun 23, 2021 N103784
F2121238 Certificate of Analysis Jun 23, 2021 N103784
H2412513 Certificate of Analysis Jun 23, 2021 N103784
H2330050 Certificate of Analysis Jun 23, 2021 N103784

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Chemical and Physical Properties

Solubility Solubility in dilute Acetic acid almost transparency;
Sensitivity Light and Air sensitive
Flash Point(°F) 314.6 °F
Flash Point(°C) 157℃
Boil Point(°C) 301°C
Melt Point(°C) 50°C
Molecular Weight 143.180 g/mol
XLogP3 2.200
Hydrogen Bond Donor Count 1
Hydrogen Bond Acceptor Count 1
Rotatable Bond Count 0
Exact Mass 143.073 Da
Monoisotopic Mass 143.073 Da
Topological Polar Surface Area 26.000 Ų
Heavy Atom Count 11
Formal Charge 0
Complexity 133.000
Isotope Atom Count 0
Defined Atom Stereocenter Count 0
Undefined Atom Stereocenter Count 0
Defined Bond Stereocenter Count 0
Undefined Bond Stereocenter Count 0
The total count of all stereochemical bonds 0
Covalently-Bonded Unit Count 1

Solution Calculators

Reviews

Customer Reviews

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