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2-IMINOBIOTIN HYDROBROMIDE

Product Name
2-IMINOBIOTIN HYDROBROMIDE
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
Formula Weight
243.33
MOL File
13395-35-2.mol
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2-IMINOBIOTIN HYDROBROMIDE Property

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
pka
4.73±0.10(Predicted)
form 
White to off-white powder.
BRN 
18952
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Safety

Safety Statements 
22-24/25
WGK Germany 
3
10-21
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
I4632
Product name
2-Iminobiotin
Purity
≥98% (TLC)
Packaging
100mg
Price
$176
Updated
2024/03/01
Cayman Chemical
Product number
20812
Product name
2-Iminobiotin
Purity
≥98%
Packaging
10mg
Price
$32
Updated
2024/03/01
Cayman Chemical
Product number
20812
Product name
2-Iminobiotin
Purity
≥98%
Packaging
50mg
Price
$78
Updated
2024/03/01
Cayman Chemical
Product number
20812
Product name
2-Iminobiotin
Purity
≥98%
Packaging
100mg
Price
$139
Updated
2024/03/01
Usbiological
Product number
280313
Product name
2-Iminobiotin
Packaging
50mg
Price
$531
Updated
2021/12/16
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2-IMINOBIOTIN HYDROBROMIDE Chemical Properties,Usage,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

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View Lastest Price from 2-IMINOBIOTIN HYDROBROMIDE manufacturers

Career Henan Chemical Co
Product
2-IMINOBIOTIN HYDROBROMIDE 13395-35-2
Price
US $5.50/KG
Min. Order
1KG
Purity
98%min
Supply Ability
1kg,10kg,100kg
Release date
2020-01-09

13395-35-2, 2-IMINOBIOTIN HYDROBROMIDERelated Search:


  • GUANIDINOBIOTIN
  • HEXAHYDRO-2-IMINO-1H-THIENO[3,4-D]IMIDAZOLE-4-PENTANOIC ACID
  • 2-IMINOBIOTIN
  • 2-IMINOBIOTIN HYDROBROMIDE
  • 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
  • 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-[(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
  • 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