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(+)-BIOTIN-EPSILON-AMINOCAPROIC ACID structure, CAS 72040-64-3

(+)-BIOTIN-EPSILON-AMINOCAPROIC ACID

CAS Number72040-64-3

SynonymsReferences

Molecular FormulaC16H27N3O4S

Molecular Weight357.47

Purity≥97.0 (HPLC)%

Density1.2g/cm3

Boiling Point721.3ºC at 760 mmHg

Melting Point220-230 °C (dec.)

Flash Point

Appearancepowder

EINECS

MSDSChineseEnglish

Symbol

Signal Word

Cat. No.: 2A-1172830 Purity: ≥97.0 (HPLC)%
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Quality Control of [ 72040-64-3 ] Purity: ≥97.0 (HPLC)% SDS Specification MoL

Chemical & Physical Properties
CAS Number72040-64-3
Catalog No.2A-1172830
Chinese NameN-生物素己酸
SynonymsReferences
Molecular FormulaC16H27N3O4S
Molecular Weight357.47
Purity≥97.0 (HPLC)
Density1.2g/cm3
Boiling Point721.3ºC at 760 mmHg
Melting Point220-230 °C (dec.)
Appearancepowder
Storage Conditionroom temperature
ApplicationN-Biotinyl-6-aminohexanoic acid (N-(+)-Biotinyl-6-aminohexanoic acid) can be used for biotinylation.
PubChem ID329750290
MDL NumberMFCD00144853
SMILES[H][C@]12CS[C@@H](CCCCC(=O)NCCCCCC(O)=O)[C@@]1([H])NC(=O)N2
InChI1S/C16H27N3O4S/c20-13(17-9-5-1-2-8-14(21)22)7-4-3-6-12-15-11(10-24-12)18-16(23)19-15/h11-12,15H,1-10H2,(H,17,20)(H,21,22)(H2,18,19,23)/t11-,12-,15-/m0/s1
InChI KeyCMUGHZFPFWNUQT-HUBLWGQQSA-N
Beilstein/REAXYS706392
NACRES CodeNA.79
UNSPSC12352106
MSDSmsds/173115_1_72040_64_3.pdf
BioactivityN-Biotinyl-6-aminohexanoic acid (N-(+)-Biotinyl-6-aminohexanoic acid) can be used to perform biotinylation[1]. Related Catalog Research Areas >> Others Signaling Pathways >> Others >> Others In Vitro Synthesis of p-nitrophenyl N-acetyllactosaminide with β-D-galactosidase, chemical reduction of the p-nitrophenyl group, and sialylation with sialyltransferase. The p-aminophenyl glycosides are then successfully biotin-labeled through the coupling with N-(+)-biotinyl-6- aminohexanoic acid to afford biotinylated oligosaccharides with an aminohexanosyl group and phenyl group as the spacers between the biotin and glycan[1]. The SERS (surface-enhanced Raman scattering) of cyclohexyl isocyanide that silver nanoparticles modified with N-(+)-biotinyl-6-aminocaproic acid and cyclohexyl isocyanide can be anchored on a separate biotinylated substrate via the avidin-biotin interaction[2]. References [1]. Zeng X, et al. Effective chemoenzymatic synthesis of p-aminophenyl glycosides of sialyl N-acetyllactosaminide and analysis of their interactions with lectins. Carbohydr Res. 2007 Jul 2;342(9):1244-8. [2]. Kim K, et al. microAg particle-based molecular sensing/recognition via surface-enhanced Raman spectroscopy. Biosens Bioelectron. 2007 Jan 15;22(6):1000-5. Chemical & Physical Properties Density 1.2g/cm3 Boiling Point 721.3ºC at 760 mmHg Melting Point 220-230ºC (dec.) Molecular Formula C16H27N3O4S Molecular Weight 357.46800 Flash Point 390ºC Exact Mass 357.17200 PSA 132.83000 LogP 2.52190 Index of Refraction 1.532 InChIKey CMUGHZFPFWNUQT-HUBLWGQQSA-N SMILES O=C(O)CCCCCNC(=O)CCCCC1SCC2NC(=O)NC21
Use ofN-Biotinyl-6-aminohexanoic acid (N-(+)-Biotinyl-6-aminohexanoic acid) can be used to perform biotinylation[1]. Properties Name N-Biotinylcaproic Acid Synonym More Synonyms N-Biotinyl-6-aminohexanoic acid Biological Activity Description N-Biotinyl-6-aminohexanoic acid (N-(+)-Biotinyl-6-aminohexanoic acid) can be used to perform biotinylation[1]. Related Catalog Research Areas >> Others Signaling Pathways >> Others >> Others In Vitro Synthesis of p-nitrophenyl N-acetyllactosaminide with β-D-galactosidase, chemical reduction of the p-nitrophenyl group, and sialylation with sialyltransferase. The p-aminophenyl glycosides are then successfully biotin-labeled through the coupling with N-(+)-biotinyl-6- aminohexanoic acid to afford biotinylated oligosaccharides with an aminohexanosyl group and phenyl group as the spacers between the biotin and glycan[1]. The SERS (surface-enhanced Raman scattering) of cyclohexyl isocyanide that silver nanoparticles modified with N-(+)-biotinyl-6-aminocaproic acid and cyclohexyl isocyanide can be anchored on a separate biotinylated substrate via the avidin-biotin interaction[2]. References [1]. Zeng X, et al. Effective chemoenzymatic synthesis of p-aminophenyl glycosides of sialyl N-acetyllactosaminide and analysis of their interactions with lectins. Carbohydr Res. 2007 Jul 2;342(9):1244-8. [2]. Kim K, et al. microAg particle-based molecular sensing/recognition via surface-enhanced Raman spectroscopy. Biosens Bioelectron. 2007 Jan 15;22(6):1000-5. Chemical & Physical Properties Molecular Formula C16H27N3O4S Exact Mass 357.17200 PSA 132.83000 LogP 2.52190 Index of Refraction 1.532 InChIKey CMUGHZFPFWNUQT-HUBLWGQQSA-N SMILES O=C(O)CCCCCNC(=O)CCCCC1SCC2NC(=O)NC21
Transport InfoProduct name: Purity: 97.0%
MSDS Transport InfoModule 14. Shipping information United Nations classification: inconsistent with United Nations classification standards UN number: not specified
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