1,5-Diaminopentane - ≥99.5% , CAS No.462-94-2

CAS: 462-94-2 Cat. No.: D283638 Formula: NH2(CH2)5NH2 Molecular Weight: 102.18 Beilstein Registry Number: 1697256 EC Number: 207-329-0
AVAILABLE TO ORDER
GRADE & PURITY ≥99.5%
Synonyms
BioDex 1- | EC 207-329-0 | UNII-L90BEN6OLL | 1,5-pentanediamine | AI3-26937 | Pentane-1,5-diamine | BBL027704 | CCG-266036 | L90BEN6OLL | MFCD00008239 | Cadaverin | 1,5-Diaminopentane | 1,5-diamino-pentane | cadaverine | DTXSID5075448 | 4-04-00-01310 (Bei
Storage
Room temperature
Shipped In
FedEx DG Service
★
Size
USA
Germany (EU)*
Price
Qty
1g
D283638-1g
1 In stock
—
$23.90
5g
D283638-5g
1 In stock
—
$56.90
25g
D283638-25g
1 In stock
—
$209.90
100g
D283638-100g
Made to order · 8–12 wks
$689.90
Enter a quantity for the sizes you want to add.
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Why this grade

≥99.5% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Room temperature Ships FedEx DG Service 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 68 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Overview

It is an important carbon five-platform compound, a colorless smoke liquid, an ammonia-like odor, soluble in water and ethanol. Using renewable plant resources as raw materials, high-purity bio-based diamines are produced through specific bio-conversion processes.

Bio-based diamines are made from renewable plant raw materials, and their bio-based content has been analyzed and verified by third-party laboratories using ASTM 6866, with a renewable carbon content of 100%, effectively reducing the use of fossil raw materials (e.g. oil), thereby reducing carbon emissions.

Evaluation parametersUnitA database of raw materials(Ecoinvent3.6)Product
nylon6nylon661,5-Diaminopentane
Global warming potential-fossilkg CO2 eq.9.90E+008.66E+007.31E+00
Global warming potential-Biological causeskg CO2 eq.1.20E-023.11E-02-5.95E+00
Global warming potential-Land use and land conversionkg CO2 eq.1.95E-051.73E-051.12E-03
Global warming potential-Totalkg CO2 eq.9.91E+008.69E+001.36E+00
Note: The above results are based on the production of 1 kg of products


Production Metrics


Procuction Features

Green, low melting point, higher reaction activity, higher product strength, brand new platform compounds

Production Apply

Can be applied to polyamide, methyl diocyanate (PDI), epoxy resin curing agent, organic synthesis intermediates, and can be further applied to spinning, engineering materials, pharmaceuticals, pesticides, organic synthesis and other fields. It has been proven to be used in automotive surface paint coatings for 14 years and has won the ECS Innovation Award.

Specifications

Synonyms
BioDex 1- | EC 207-329-0 | UNII-L90BEN6OLL | 1,5-pentanediamine | AI3-26937 | Pentane-1,5-diamine | BBL027704 | CCG-266036 | L90BEN6OLL | MFCD00008239 | Cadaverin | 1,5-Diaminopentane | 1,5-diamino-pentane | cadaverine | DTXSID5075448 | 4-04-00-01310 (Bei
Specifications & Purity
≥99.5%
Storage
Room temperature
Shipped In
FedEx DG Service
Purity
≥99.5%
Names and Identifiers
Pubchem Sid
Pubchem Sid Url
https://pubchem.ncbi.nlm.nih.gov/substance/504750372
Canonical Smiles
C(CCN)CCN
IUPAC Name
pentane-1,5-diamine
InChIKey
VHRGRCVQAFMJIZ-UHFFFAOYSA-N
INCHI
1S/C5H14N2/c6-4-2-1-3-5-7/h1-7H2
Isomeric SMILES
C(CCN)CCN
WGK Germany
3
RTECS
SA0200000
UN Number
2735
Packing Group
III
Molecular Weight
102.18
Beilstein
1697256
Reaxy-Rn
1697256
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1697256&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
SuperclassOrganic nitrogen compounds
ClassOrganonitrogen compounds
SubclassAmines
Intermediate Tree Nodes Primary amines
Direct ParentMonoalkylamines
Alternative Parents Organopnictogen compounds  Hydrocarbon derivatives  
Molecular FrameworkAliphatic acyclic compounds
Substituents Organopnictogen compound - Hydrocarbon derivative - Primary aliphatic amine - Aliphatic acyclic compound
DescriptionThis compound belongs to the class of organic compounds known as monoalkylamines. These are organic compounds containing an primary aliphatic amine group.
External Descriptors an aliphatic α,ω-diamine
3D Structure
Interactive Chemical Structure Model





Associated Targets(Human)
CA5A Tclin Carbonic anhydrase 5A, mitochondrial (1 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
CA5B Tclin Carbonic anhydrase 5B, mitochondrial (1 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
CA6 Tclin Carbonic anhydrase 6 (1 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
CA3 Tclin Carbonic anhydrase 3 (1 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
CA4 Tclin Carbonic anhydrase 4 (1 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
CA12 Tclin Carbonic anhydrase 12 (1 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
CA14 Tclin Carbonic anhydrase 14 (1 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
CA9 Tclin Carbonic anhydrase 9 (1 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
CA7 Tclin Carbonic anhydrase 7 (1 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
CA2 Tclin Carbonic anhydrase II (17698 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA3 Tclin Carbonic anhydrase III (753 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA6 Tclin Carbonic anhydrase VI (993 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA1 Tclin Carbonic anhydrase I (13240 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA5B Tclin Carbonic anhydrase VB (957 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA5A Tclin Carbonic anhydrase VA (1168 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA14 Tclin Carbonic anhydrase XIV (1305 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA12 Tclin Carbonic anhydrase XII (6231 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA9 Tclin Carbonic anhydrase IX (8255 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
POLK Tbio DNA polymerase kappa (8653 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Associated Targets(non-human)
Ca7 Carbonic anhydrase VII (3 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Ca13 Carbonic anhydrase XIII (322 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA4 Carbonic anhydrase IV (1713 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mycobacterium tuberculosis (203094 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Plasmodium falciparum (966862 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
J774 (3120 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
rep Replicase polyprotein 1ab (378 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Ca15 Carbonic anhydrase 15 (173 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mechanisms of Action
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.

16 results found

Lot NumberCertificate TypeDateItem
H2619089Certificate of AnalysisAug 27, 2026 D283638
H2619094Certificate of AnalysisAug 27, 2026 D283638
H2619072Certificate of AnalysisAug 26, 2026 D283638
H2619071Certificate of AnalysisAug 22, 2026 D283638
F2610085Certificate of AnalysisJun 18, 2026 D283638
G2606081Certificate of AnalysisJun 18, 2026 D283638
A2616077Certificate of AnalysisJan 22, 2026 D283638
D2608015Certificate of AnalysisJan 22, 2026 D283638
K2109262Certificate of AnalysisAug 12, 2025 D283638
K2109263Certificate of AnalysisAug 12, 2025 D283638
C2620125Certificate of AnalysisOct 08, 2021 D283638
D2306102Certificate of AnalysisOct 08, 2021 D283638
F2505074Certificate of AnalysisOct 08, 2021 D283638
F2516065Certificate of AnalysisOct 08, 2021 D283638
F2520011Certificate of AnalysisOct 08, 2021 D283638
K2421084Certificate of AnalysisOct 08, 2021 D283638
Chemical and Physical Properties
SolubilitySoluble in water, alchol, microsoluble in ether.
SensitivityAir & Moisture Sensitive
Refractive Index1.4585
Flash Point(°F)143.6 °F
Flash Point(°C)62 °C
Boil Point(°C)180°C
Melt Point(°C)9.34°C
Molecular Weight102.180 g/mol
XLogP3-0.600
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count2
Rotatable Bond Count4
Exact Mass102.116 Da
Monoisotopic Mass102.116 Da
Topological Polar Surface Area52.000 Ų
Heavy Atom Count7
Formal Charge0
Complexity25.300
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Documents & Articles
Citations of This Product
Solution Calculators
Reviews

Customer Reviews

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