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810104P

Avanti

palmitic acid - lissamine rhodamine

Avanti Research - A Croda Brand 810104P, powder

Synonym(s):

[16-N-(lissamine rhodamine β sulfonyl)amino] palmitic acid

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About This Item

Empirical Formula (Hill Notation):
C43H61N3O8S2
CAS Number:
Molecular Weight:
812.09
UNSPSC Code:
12352211
NACRES:
NA.25

Assay

>99% (TLC)

form

powder

packaging

pkg of 1 × 1 mg (810104P-1mg)

manufacturer/tradename

Avanti Research - A Croda Brand 810104P

shipped in

dry ice

storage temp.

−20°C

General description

Palmitic acid (PA), a saturated fatty acid, seen in human body accounts for 20−30% of total fatty acids. It can be supplied through diet or produced endogenously from other fatty acids, carbohydrates and amino acids. PA is an important constituent of palm oil. Lissamine rhodamine is a red-emitting fluorophore, mainly used in immunofluorescence studies.

Packaging

5 mL Amber Glass Screw Cap Vial (810104P-1mg)

Legal Information

Avanti Research is a trademark of Avanti Polar Lipids, LLC

Storage Class Code

11 - Combustible Solids

WGK

WGK 3


Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

810104P-1MG:
810104P-VAR:
810104P-BULK:


Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Which fluorophore is brightest? A comparison of the staining obtained using fluorescein, tetramethylrhodamine, lissamine rhodamine, Texas red, and cyanine 3.18
Wessendorf MW and Brelje TC
Histochemistry, 98(2) (1992)
Palmitic acid: Physiological role, metabolism and nutritional implications
Carta G, et al.
The Journal of Physiology (2017)
Which fluorophore is brightest? A comparison of the staining obtained using fluorescein, tetramethylrhodamine, lissamine rhodamine, Texas red, and cyanine 3.18
Wessendorf MW and Brelje TC
Histochemistry (1992)
Palmitic acid: Physiological role, metabolism and nutritional implications
Carta G, et al.
Frontiers in Physiology, 8, 902-902 (2017)

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