803332

Sulfo-SANPAH (sulfosuccinimidyl 6-(4′-azido-2′-nitrophenylamino)hexanoate)

Manufacturer: Sigma Aldrich

Synonym(S): (sulfosuccinimidyl 6-(4′-azido-2′-nitrophenylamino)hexanoate), 1-[[6-[(4-azido-2-nitrophenyl)amino]-1-oxohexyl]oxy]-2,5-dioxo-3-pyrrolidinesulfonic acid monosodium salt, Sulfo-SANPAH

Select a Size

Pack Size SKU Availability Price
50 MG 803332-50-MG In Stock ₹ 39,511.25

803332 - 50 MG

₹ 39,511.25

In Stock

Quantity

1

Base Price: ₹ 39,511.25

GST (18%): ₹ 7,112.025

Total Price: ₹ 46,623.275

form

powder

Quality Level

100

mol wt

492.4

reaction suitability

reagent type: cross-linking reagent

storage condition

desiccated

solubility

water: soluble

functional group

azide

shipped in

ambient

storage temp.

−20°C

SMILES string

O=C1CC(S(=O)([O-])=O)C(N1OC(CCCCCNC2=CC=C(N=[N+]=[N-])C=C2[N+]([O-])=O)=O)=O.[Na+]

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Description

  • General description: ANB-NOS and Sulfo-SANPAH are heterobifunctional crosslinkers that contain an amine-reactive N-hydroxysuccinimide (NHS) ester and a photoactivatable nitrophenyl azide. NHS esters react efficiently with primary amino groups (-NH2) in pH 7-9 buffers to form stable amide bonds. When exposed to UV light nitrophenyl azides form a nitrene group that can initiate addition reactions with double bonds, insertion into C-H and N-H sites, or subsequent ring expansion to react with a nucleophile (e.g., primary amines).
  • Application: Dynamic Control of Cell Adhesion on a Stiffness-Tunable Substrate for Analyzing the Mechanobiology of Collective Cell Migration: This study uses Sulfo-SANPAH for photochemical cross-linking in cell adhesion research (Kamimura et al., 2017). Evaluation of L929 fibroblast attachment and proliferation on ArgGlyAspSer (RGDS) immobilized chitosan: This paper investigates the use of Sulfo-SANPAH to enhance fibroblast attachment on chitosan substrates (Karakecili et al., 2016).
  • Features and Benefits: Reactive groups: sulfo-NHS ester and nitrophenyl azideReactive towards: amino groups and any nucleophileNon-cleavableN-Sulfosuccinimidyl-6-(4′-azido-2′-nitrophenylamino) hexanoateOptimal photolysis occurs at 320-350 nm; minimizes damage to biomolecules by irradiationWater soluble; non-cleavable
  • Caution: This product is sensitive to moisture. The vial is packaged in a resealable bag with a desiccant to reduce exposure to moisture. After cold storage, equilibrate the vial to room temperature before opening to reduce condensation inside the vial. Make fresh solutions. Storage of stock solutions is not recommended. After use, return the vial to the resealable bag. Close the bag and store the product at the recommended temperature.

SAFETY INFORMATION

Pictograms

GHS07

Signal Word

Warning

Hazard Statements

H319

Precautionary Statements

P264 - P280 - P305 + P351 + P338 - P337 + P313

Hazard Classifications

Eye Irrit. 2

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

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Show Difference

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Sigma Aldrich

803332

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form:
powder

Quality Level:
100

mol wt:
492.4

reaction suitability:
reagent type: cross-linking reagent

storage condition:
desiccated

solubility:
water: soluble

functional group:
azide

shipped in:
ambient

storage temp.:
−20°C

SMILES string:
O=C1CC(S(=O)([O-])=O)C(N1OC(CCCCCNC2=CC=C(N=[N+]=[N-])C=C2[N+]([O-])=O)=O)=O.[Na+]

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Sigma Aldrich

803340

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form:
powder

Quality Level:
100

mol wt:
327.25

reaction suitability:
reagent type: cross-linking reagent

storage condition:
desiccated

solubility:
water: soluble

functional group:
__

shipped in:
ambient

storage temp.:
2-8°C

SMILES string:
O=C(C(S(=O)([O-])=O)C1)N(OC(CCC2(N=N2)C)=O)C1=O.[Na+]

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Sigma Aldrich

803359

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powder

Quality Level:
100

mol wt:
440.4

reaction suitability:
reagent type: cross-linking reagent

storage condition:
desiccated

solubility:
water: soluble

functional group:
__

shipped in:
ambient

storage temp.:
2-8°C

SMILES string:
O=C(N1OC(CCCCCNC(CCC2(N=N2)C)=O)=O)CC(S(=O)([O-])=O)C1=O.[Na+]

Img

Supelco

80342

analytical standard...


form:
__

Quality Level:
100

mol wt:
__

reaction suitability:
__

storage condition:
__

solubility:
__

functional group:
__

shipped in:
__

storage temp.:
__

SMILES string:
C[C@@H]1CC[C@]2(C)CC[C@]3(C)C(=CC[C@@H]4[C@@]5(C)CC[C@@H](O)[C@@](C)([C@@H]5CC[C@@]34C)C(O)=O)[C@@H]2[C@H]1C