Gonadorelin Acetate - ≥98% , CAS No.71447-49-9

CAS: 71447-49-9 Cat. No.: G416682 Peso molecular: 1302.4 Número EC: 636-116-9 PubChem CID: 56841073
Disponible para pedir
GRADE & PURITY ≥98%
Synonyms
LHRH diacetate | S-71447-49-9 | LH-RH, human | AKOS030485979 | Gonadorelin diacetate | Gonadorelin Acetate (33515-09-2 free base) | Gonadorelin diacetate (JP17) | AKOS040758695 | UNII-7AT6GVO7OA | DTXSID201339012 | 7AT6GVO7OA | D03267
Storage
Store at -20°C
Shipped In
Ice chest + Ice pads
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
10mg
G416682-10mg
2

82,90US$

92,90US$
Guardar 10,00 US$ (10.76%)
50mg
G416682-50mg
1
264,90US$
100mg
G416682-100mg
2
395,90US$
Enter a quantity for the sizes you want to add.
🧪

Why this grade

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

🌡

Storage & shipping

Store at -20°C Ships Ice chest + Ice pads 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

Gonadorelin Acetate (33515-09-2 free base) (Luteinizing Hormone Releasing Hormone (LH-RH)) is hypothalamic neuropeptide which plays a key role in the control of reproductive functions.

Specifications

Sinónimos
LHRH diacetate | S-71447-49-9 | LH-RH, human | AKOS030485979 | Gonadorelin diacetate | Gonadorelin Acetate (33515-09-2 free base) | Gonadorelin diacetate (JP17) | AKOS040758695 | UNII-7AT6GVO7OA | DTXSID201339012 | 7AT6GVO7OA | D03267
Especificaciones y pureza
≥98%
Condiciones de almacenamiento de almacenamiento
Store at -20°C
Enviado en
Ice chest + Ice pads
Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.
Pureza
≥98%
Nombres e identificadores
Pubchem Sid504771465
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504771465
Sonrisas canónicasCC(C)CC(C(=O)NC(CCCN=C(N)N)C(=O)N1CCCC1C(=O)NCC(=O)N)NC(=O)CNC(=O)C(CC2=CC=C(C=C2)O)NC(=O)C(CO)NC(=O)C(CC3=CNC4=CC=CC=C43)NC(=O)C(CC5=CN=CN5)NC(=O)C6CCC(=O)N6.CC(=O)O.CC(=O)O
IUPAC Nameacetic acid;(2S)-N-[(2S)-1-[[(2S)-1-[[(2S)-1-[[(2S)-1-[[2-[[(2S)-1-[[(2S)-1-[(2S)-2-[(2-amino-2-oxoethyl)carbamoyl]pyrrolidin-1-yl]-5-(diaminomethylideneamino)-1-oxopentan-2-yl]amino]-4-methyl-1-oxopentan-2-yl]amino]-2-oxoethyl]amino]-3-(4-hydroxyphenyl)-1-oxopropan-2-yl]amino]-3-hydroxy-1-oxopropan-2-yl]amino]-3-(1H-indol-3-yl)-1-oxopropan-2-yl]amino]-3-(1H-imidazol-5-yl)-1-oxopropan-2-yl]-5-oxopyrrolidine-2-carboxamide
InChIKeyQOVPLTBEZAJSHY-VIRDRFNDSA-N
INCHI1S/C55H75N17O13.2C2H4O2/c1-29(2)19-38(49(80)67-37(9-5-17-60-55(57)58)54(85)72-18-6-10-43(72)53(84)62-25-44(56)75)66-46(77)26-63-47(78)39(20-30-11-13-33(74)14-12-30)68-52(83)42(27-73)71-50(81)40(21-31-23-61-35-8-4-3-7-34(31)35)69-51(82)41(22-32-24-59-28-64-32)70-48(79)36-15-16-45(76)65-36;2*1-2(3)4/h3-4,7-8,11-14,23-24,28-29,36-43,61,73-74H,5-6,9-10,15-22,25-27H2,1-2H3,(H2,56,75)(H,59,64)(H,62,84)(H,63,78)(H,65,76)(H,66,77)(H,67,80)(H,68,83)(H,69,82)(H,70,79)(H,71,81)(H4,57,58,60);2*1H3,(H,3,4)/t36-,37-,38-,39-,40-,41-,42-,43-;;/m0../s1
Isómeros SMILES CC(C)C[C@@H](C(=O)N[C@@H](CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)NCC(=O)N)NC(=O)CNC(=O)[C@H](CC2=CC=C(C=C2)O)NC(=O)[C@H](CO)NC(=O)[C@H](CC3=CNC4=CC=CC=C43)NC(=O)[C@H](CC5=CN=CN5)NC(=O)[C@@H]6CCC(=O)N6.CC(=O)O.CC(=O)O
CAS alternativo 33515-09-2;51952-41-1
PubChem CID 56841073
Peso molecular 1302.4

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 Polymers
ClasePolypeptides
SubclassNot available
Intermediate Tree Nodes Not available
Direct ParentPolypeptides
Alternative Parents Peptides  Tyrosine and derivatives  Phenylalanine and derivatives  Histidine and derivatives  Leucine and derivatives  N-acyl-alpha amino acids and derivatives  Proline and derivatives  Alpha amino acid amides  Serine and derivatives  Tryptamines and derivatives  3-alkylindoles  Amphetamines and derivatives  Pyrrolidinecarboxamides  N-acylpyrrolidines  1-hydroxy-2-unsubstituted benzenoids  Pyrrolidine-2-ones  Substituted pyrroles  N-acyl amines  Heteroaromatic compounds  Imidazoles  Tertiary carboxylic acid amides  Lactams  Secondary carboxylic acid amides  Guanidines  Primary carboxylic acid amides  Propargyl-type 1,3-dipolar organic compounds  Carboxylic acids  Carboximidamides  Azacyclic compounds  Monocarboxylic acids and derivatives  Hydrocarbon derivatives  Organopnictogen compounds  Carbonyl compounds  Primary alcohols  Organic oxides  
Molecular FrameworkNot available
Substituents Polypeptide - Alpha peptide - Tyrosine or derivatives - Phenylalanine or derivatives - Histidine or derivatives - Leucine or derivatives - N-acyl-alpha amino acid or derivatives - Proline or derivatives - Triptan - Alpha-amino acid amide - Serine or derivatives - Amphetamine or derivatives - Alpha-amino acid or derivatives - 3-alkylindole - N-substituted-alpha-amino acid - Indole - Indole or derivatives - N-acylpyrrolidine - Pyrrolidine carboxylic acid or derivatives - Pyrrolidine-2-carboxamide - Phenol - 1-hydroxy-2-unsubstituted benzenoid - Benzenoid - Monocyclic benzene moiety - Fatty acyl - Fatty amide - Substituted pyrrole - N-acyl-amine - 2-pyrrolidone - Pyrrolidone - Azole - Tertiary carboxylic acid amide - Imidazole - Heteroaromatic compound - Pyrrolidine - Pyrrole - Primary carboxylic acid amide - Carboxamide group - Guanidine - Lactam - Secondary carboxylic acid amide - Azacycle - Propargyl-type 1,3-dipolar organic compound - Carboximidamide - Carboxylic acid derivative - Carboxylic acid - Organoheterocyclic compound - Organic 1,3-dipolar compound - Monocarboxylic acid or derivatives - Primary alcohol - Organonitrogen compound - Carbonyl group - Organopnictogen compound - Organic nitrogen compound - Alcohol - Organic oxide - Hydrocarbon derivative - Organic oxygen compound - Organooxygen compound - Aromatic heteropolycyclic compound
DescripciónThis compound belongs to the class of organic compounds known as polypeptides. These are peptides containing ten or more amino acid residues.
External Descriptors Not available
Estructura 3D
Modelo de Estructura Química Interactiva





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.

7 results found

Lot NumberCertificate TypeFechaArticulo
L2523417Certificate of AnalysisNov 08, 2025 G416682
L2523418Certificate of AnalysisNov 08, 2025 G416682
L2523419Certificate of AnalysisNov 08, 2025 G416682
H2220248Certificate of AnalysisJun 09, 2025 G416682
H2220249Certificate of AnalysisJun 09, 2025 G416682
H2220352Certificate of AnalysisJun 09, 2025 G416682
I2424109Certificate of AnalysisMay 22, 2022 G416682
Propiedades químicas y físicas
Peso molecular1302.400 g/mol
XLogP3
Hydrogen Bond Donor Count18
Hydrogen Bond Acceptor Count19
Rotatable Bond Count31
Exact Mass1301.62 Da
Monoisotopic Mass1301.62 Da
Topological Polar Surface Area549.000 Ų
Heavy Atom Count93
Formal Charge0
Complexity2420.000
Isotope Atom Count0
Defined Atom Stereocenter Count8
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count3
Calculadoras de soluciones
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