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2-IMINOBIOTIN HYDROBROMIDE

2-IMINOBIOTIN HYDROBROMIDE Structure
CAS No.
13395-35-2
Chemical Name:
2-IMINOBIOTIN HYDROBROMIDE
Synonyms
2-IMINOBIOTIN;Iminobiotin;2-Iminobiotine;GUANIDINOBIOTIN;2-IMINOBIOTIN 98+%;2- Iminobiotin 13395-35-2;2-Iminobiotin >=98% (TLC);2-IMINOBIOTIN HYDROBROMIDE;Tetrahydro-2-iminothieno[3,4-d]imidazoline-4-valeric acid;HEXAHYDRO-2-IMINO-1H-THIENO[3,4-D]IMIDAZOLE-4-PENTANOIC ACID
CBNumber:
CB7157057
Molecular Formula:
C10H17N3O2S
Molecular Weight:
243.33
MOL File:
13395-35-2.mol
MSDS File:
SDS
Modify Date:
2024/7/2 8:55:16
Request For Quotation

2-IMINOBIOTIN HYDROBROMIDE Properties

Boiling point 477.3±55.0 °C(Predicted)
Density 1.60
storage temp. 2-8°C
solubility 1 M HCl: 50 mg/mL, clear, colorless
form White to off-white powder.
pka 4.73±0.10(Predicted)
color White to off-white
BRN 18952

SAFETY

Risk and Safety Statements

Safety Statements  22-24/25
WGK Germany  3
F  10-21

2-IMINOBIOTIN HYDROBROMIDE price More Price(1)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) I4632 2-Iminobiotin ≥98% (TLC) 13395-35-2 100MG ₹16854.53 2022-06-14 Buy
Product number Packaging Price Buy
I4632 100MG ₹16854.53 Buy

2-IMINOBIOTIN HYDROBROMIDE Chemical Properties,Uses,Production

Uses

2-Iminobiotin has been used as a competitive inhibitor to bind to biotic binding sites on streptavidin in order to restore fluorescence signal.

General Description

2-Iminobiotin is a cyclic guanidino analog of biotin that has high affinity for avidin at high pH (>9) and low affinity at low pH (<6). The proteins that are iminobiotinylated are selectively contained within the avidin column at pH 9 to 11 and may be eluted at pH 4 or by the addition of biotin. This technique may be very useful in the study of cell surface proteins by labeling and selectively recovering the components that are periodate-sensitive from intact human erythrocyte surface. 2-Iminobiotin reversibly inhibits NOS (nitric oxide synthases) via its guanidino group. It inhibits NO biosynthesis and may be important to understand the binding-site interactions for this important class of enzymes. NOS oxidizes the guanidino-nitrogen of L-arginine to produce nitric oxide and L-citrulline.

2-IMINOBIOTIN HYDROBROMIDE Preparation Products And Raw materials

Raw materials

Preparation Products

2-IMINOBIOTIN HYDROBROMIDE Suppliers

Global( 97)Suppliers
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A.J Chemicals 91-9810153283 New Delhi, India 6124 58 Inquiry
BOC Sciences +1-631-485-4226 United States 19553 58 Inquiry
CONIER CHEM AND PHARMA LIMITED +8618523575427 China 49403 58 Inquiry
career henan chemical co +86-0371-86658258 +8613203830695 China 29820 58 Inquiry
Hefei TNJ Chemical Industry Co.,Ltd. +86-0551-65418671 +8618949823763 China 34571 58 Inquiry
Dayang Chem (Hangzhou) Co.,Ltd. 571-88938639 +8617705817739 China 52861 58 Inquiry
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TargetMol Chemicals Inc. +1-781-999-5354 United States 19973 58 Inquiry
PT CHEM GROUP LIMITED China 35426 58 Inquiry
Supplier Advantage
A.J Chemicals 58
BOC Sciences 58
CONIER CHEM AND PHARMA LIMITED 58
career henan chemical co 58
Hefei TNJ Chemical Industry Co.,Ltd. 58
Dayang Chem (Hangzhou) Co.,Ltd. 58
Henan Alfa Chemical Co., Ltd 58
Labnetwork lnc. 58
TargetMol Chemicals Inc. 58
PT CHEM GROUP LIMITED 58

13395-35-2(2-IMINOBIOTIN HYDROBROMIDE)Related Search:

3-BROMO-7-NITROINDAZOLE N'-Nitro-L-arginine-methyl ester hydrochloride NG,NG-DIMETHYL-L-ARGININE DIHYDROCHLORIDE L-N5-(1-IMINOETHYL)ORNITHINE*HYDROCHLORI DE Aminoguanidine bicarbonate
NG-MONOMETHYL-L-ARGININE ACETATE AMINOGUANIDINE HEMISULFATE IroMycin A 7-NINA L-N6-(1-IMINOETHYL)LYSINE DIHYDROCHLORIDE
L-THIOCITRULLINE DIHYDROCHLORIDE L-NAA HCL S-ISOPROPYLTHIOUREA HYDROBROMIDE 2-IMINOBIOTIN HYDROBROMIDE 2-IMINOBIOTIN N-HYDROXYSUCCINIMIDE ESTER
2-Iminobiotin N-hydroxysuccinimide ester hydrobromide NHS-IMINOBIOTIN TRIFLUOROACETAMIDE NHS-IMINOBIOTIN
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GUANIDINOBIOTIN HEXAHYDRO-2-IMINO-1H-THIENO[3,4-D]IMIDAZOLE-4-PENTANOIC ACID 2-IMINOBIOTIN HYDROBROMIDE 2-Iminobiotine 2-IMINOBIOTIN 98+% Guanidinobiotin, Hexahydro-2-imino-1H-thieno[3,4-d]imidazole-4-pentanoic acid (3aR,6S,6aS)-2-Amino-3a,4,6,6a-tetrahydro-1H-thieno[3,4-d]imidazole-6-pentanoic acid Iminobiotin 1H-Thieno[3,4-d]iMidazole-6-pentanoicacid, 2-aMino-3a,4,6,6a-tetrahydro-, (3aR,6S,6aS)- Iminobiotin (3aR,6S,6aS)-2-Amino-3a,4,6,6a-tetrahydro-1H-thieno[3,4-d]imidazole-6-pentanoic acid 5-((2S,3S,4R)-3,4-diaminotetrahydrothiophen-2-yl)pentanoic acid compound with sulfuric acid (1:1) 5-((3aR,6S,6aS)-2-Amino-3a,4,6,6a-tetrahydro-1H-thieno[3,4-d]imidazol-6-yl)pentanoic acid Tetrahydro-2-iminothieno[3,4-d]imidazoline-4-valeric acid 5-[(3aS,4S,6aR)-2-amino-3a,4,6,6a-tetrahydro-1H-thieno[3,4-d]imidazol-4-yl]pentanoic acid 2- Iminobiotin 13395-35-2 5-[(3aS,4S,6aR)-2-imino-hexahydro-1H-thieno[3,4-d]imidazolidin-4-yl]pentanoic acid 2-Iminobiotin >=98% (TLC) 5-((3aS,4S,6aR)-2-iminohexahydro-1H-thieno[3,4-d]imidazol-4-yl)pentanoic acid 2-IMINOBIOTIN 13395-35-2 Enzymes, Inhibitors, and Substrates Enzyme Inhibitors by Type Enzyme Inhibitors Enzyme Inhibitors by Enzyme L to O Nitric Oxide Synthase Other Biochemicals and Reagents BioChemical