(R)-Sulforaphane - Moligand™, ≥98% , CAS No.142825-10-3

CAS: 142825-10-3 Cat. No.: R131741 Molecular Weight: 177.29
AVAILABLE TO ORDER
GRADE & PURITY Moligand™ ? Moligand™ — Aladdin's line of ligands and bioactive small molecules. Use for receptor, pathway, and binding studies needing defined small-molecule tools. ≥98%
Synonyms
HY-13755A | 1-isothiocyanato-4-[(R)-methanesulfinyl]butane | 1-Propanamine, 2-chloro-N,N-dimethyl-, hydrochloride (1:1) | (R)-1-Isothiocyanato-4-(methylsulfinyl)butane | GA49J4310U | 2-Piperidinemethanol, 97% | SULFORAPHANE [MI] | SULFORAPHANE [INCI] | (R
Storage
Protected from light,Store at -20°C
Shipped In
Ice chest + Ice pads
 ·  off list, applied to all prices below.
Size
Status
Price
Qty
5mg
R131741-5mg
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.
$149.90
10mg
R131741-10mg
2
$229.90
Enter a quantity for the sizes you want to add.
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Why this grade

Moligand™, ≥98% Moligand™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Protected from light,Store at -20°C Ships Ice chest + Ice pads Check lot-specific COA for exact specifications.

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Quality documents

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

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Literature proof

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

Overview

L-Sulforaphane, a compound found at high levels in broccoli, has been reported to prevent NFκB binding, which results in downregulation of apoptosis inhibitors therefore inducing apoptosis. Research has demonstrated sulforaphane to be a potent inducer of phase II detoxification enzymes and display chemoprotective properties. Other experiments have shown sulforaphane to induce enzymes of xenobiotic metabolism and therefore accelerate the metabolic disposal of xenobiotics. Sulforaphane also displays a capacity to inhibit intracellular, extracellular, and antibiotic-resistant strains of Helicobacter pylori. Additionally, this compound has been found to prevent clonogenicity. This product is sold in the L-enantiomer form.
An inducer of apoptosis, detoxification and xenobiotic enzymes

Specifications

Synonyms
HY-13755A | 1-isothiocyanato-4-[(R)-methanesulfinyl]butane | 1-Propanamine, 2-chloro-N, N-dimethyl-, hydrochloride (1:1) | (R)-1-Isothiocyanato-4-(methylsulfinyl)butane | GA49J4310U | 2-Piperidinemethanol, 97% | SULFORAPHANE [MI] | SULFORAPHANE [INCI] | (R
Specifications & Purity
Moligand™, ≥98%
Biochemical and Physiological Mechanisms
Non-competitive antagonist of the aryl hydrocarbon receptor. Natural isothiocyanate. Antioxidant, promotes cell proliferation, reduces senescence and apoptosis. Upregulates CYP1A1/1B1 apoprotein levels in vivo . Chemopreventive.
Storage
Protected from light, Store at -20°C
Shipped In
Ice chest + Ice pads
This product requires cold chain shipping. Ground and other economy services are not available.
Grade
Moligand™
Action Type
INHIBITOR
Note
Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.
Purity
≥98%
Names and Identifiers
Canonical SmilesCS(=O)CCCCN=C=S
IUPAC Name1-isothiocyanato-4-[(R)-methylsulfinyl]butane
InChIKeySUVMJBTUFCVSAD-SNVBAGLBSA-N
INCHI1S/C6H11NOS2/c1-10(8)5-3-2-4-7-6-9/h2-5H2,1H3/t10-/m1/s1
Isomeric SMILES C[S@@](=O)CCCCN=C=S
WGK Germany 3
Molecular Weight 177.29
Reaxy-Rn 1723237
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1723237&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
SuperclassOrganosulfur compounds
ClassSulfoxides
SubclassNot available
Intermediate Tree Nodes Not available
Direct ParentSulfoxides
Alternative Parents Isothiocyanates  Sulfinyl compounds  Propargyl-type 1,3-dipolar organic compounds  Organopnictogen compounds  Organonitrogen compounds  Organic oxides  Hydrocarbon derivatives  
Molecular FrameworkAliphatic acyclic compounds
Substituents Sulfoxide - Isothiocyanate - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Sulfinyl compound - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organonitrogen compound - Aliphatic acyclic compound
DescriptionThis compound belongs to the class of organic compounds known as sulfoxides. These are compounds containing a sulfoxide functional group, with the structure RS(=O)R' (R,R' not H).
External Descriptors sulforaphane
3D Structure
Interactive Chemical Structure Model





Associated Targets(Human)
NFE2L2 Tchem Nuclear factor erythroid 2-related factor 2 (1 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
VDR Tclin Vitamin D receptor (26531 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MRC5 (9203 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
A549 (127892 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HaCaT (4069 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
APEX1 Tchem DNA-(apurinic or apyrimidinic site) lyase (38016 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Associated Targets(non-human)
Nqo1 NAD(P)H dehydrogenase [quinone] 1 (1058 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
rep Replicase polyprotein 1ab (378 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Nfe2l2 Nuclear factor erythroid 2-related factor 2 (214 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Rorc Nuclear receptor ROR-gamma (89407 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.

3 results found

Lot NumberCertificate TypeDateItem
L2529243Certificate of AnalysisDec 15, 2025 R131741
F2524554Certificate of AnalysisJun 10, 2025 R131741
F1515081Certificate of AnalysisJan 25, 2023 R131741
Chemical and Physical Properties
SolubilitySoluble in DMSO (>5 mg/ml), 100% ethanol, methanol, chloroform, and ethyl acetate.
Sensitivitylight sensitive
Molecular Weight177.300 g/mol
XLogP31.400
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count4
Rotatable Bond Count5
Exact Mass177.028 Da
Monoisotopic Mass177.028 Da
Topological Polar Surface Area80.700 Ų
Heavy Atom Count10
Formal Charge0
Complexity152.000
Isotope Atom Count0
Defined Atom Stereocenter Count1
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
Solution Calculators
Reviews

Customer Reviews

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