860347P

14:0 PC-d63

Manufacturer: Sigma Aldrich

CAS Number: 326495-30-1

Synonym(S): 1,2-Dimyristoyl-d54-sn-glycero-3-phosphocholine-N,N,N-trimethyl-d9

Select a Size

Pack Size SKU Availability Price
10 MG 860347P-10-MG In Stock ₹ 1,39,112.08

860347P - 10 MG

₹ 1,39,112.08

In Stock

Quantity

1

Base Price: ₹ 1,39,112.08

GST (18%): ₹ 25,040.174

Total Price: ₹ 1,64,152.254

Assay

>99% (TLC)

form

powder

packaging

pkg of 1 × 10 mg (860347P-10MG)

manufacturer/tradename

Avanti Polar Lipids

shipped in

dry ice

storage temp.

−20°C

SMILES string

[H][C@@](COP([O-])(OCC[N+](C([2H])([2H])[2H])(C([2H])([2H])[2H])C([2H])([2H])[2H])=O)(OC(C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2

Other Options

Image Product Name Manufacturer Price Range
BL09874
326495-30-1 | 1,2-dimyristoyl-d54-sn-glycero-3-phosphocholine-N,N,N-trimethyl-d9
A2B Chem ₹ 94,458.24

Related Products

Img

Sigma Aldrich

860368P

--

Img

Sigma Aldrich

860352P

--

Img

Sigma Aldrich

860341P

--

Img

Sigma Aldrich

860371P

--

Img

Sigma Aldrich

860358P

--

Img

Sigma Aldrich

860353P

--

Img

Sigma Aldrich

860357P

--

Img

Sigma Aldrich

850851P

--

Description

  • General description: Phosphatidylcholine (PC) (Lecithins) has two fatty acid chains attached to a head group. Generally, PC has saturated fatty acid in the sn-1 position and unsaturated fatty acid in the sn-2 position. It has a quaternary ammonium group and a phosphate moiety in the head group, existing as a zwitterion in a wide range of pH. The fatty acid in PC is mostly palmitic, stearic, oleic, linolenic and arachidonic acid.[1] It is present abundantly in the mammalian membranes.[2] PC is principally synthesized from cytidine diphosphate-choline (CDP-choline).[1] Selective deuteration of this lipid may be used in the structural studies using techniques such as nuclear magnetic resonance (NMR), neutron reflectivity and small-angle neutron scattering.[3]
  • Biochem/physiol Actions: Phosphatidylcholine (PC) is essential for cholesterol trafficking and membrane cholesterol homeostasis. It acts as the precursor for the synthesis of sphingomyelin.[4] PC plays a key role in the synthesis of second messenger and signaling molecules like diacyl glycerol, lysophosphatidic acid, phosphatidic acid and arachidonic acid.[5]
  • Packaging: 5 mL Amber Glass Screw Cap Vial (860347P-10MG)

SAFETY INFORMATION

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Compare Similar Items

Show Difference

Img

Sigma Aldrich

860347P

--


Assay:
>99% (TLC)

form:
powder

packaging:
pkg of 1 × 10 mg (860347P-10MG)

manufacturer/tradename:
Avanti Polar Lipids

shipped in:
dry ice

storage temp.:
−20°C

SMILES string:
[H][C@@](COP([O-])(OCC[N+](C([2H])([2H])[2H])(C([2H])([2H])[2H])C([2H])([2H])[2H])=O)(OC(C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2

Img

Sigma Aldrich

860351P

--


Assay:
>99% (TLC)

form:
powder

packaging:
pkg of 1 × 10 mg (860351P-10MG)

manufacturer/tradename:
Avanti Polar Lipids

shipped in:
dry ice

storage temp.:
−20°C

SMILES string:
[H][C@@](COP([O-])(OC([2H])([2H])C([2H])([2H])[N+](C)(C)C)=O)(OC(CCCCCCCCCCCCCCC)=O)COC(CCCCCCCCCCCCCCC)=O

Img

Sigma Aldrich

860352P

--


Assay:
>99% (TLC)

form:
powder

packaging:
pkg of 1 × 10 mg (860352P-10mg)

manufacturer/tradename:
Avanti Polar Lipids 860352P

shipped in:
dry ice

storage temp.:
−20°C

SMILES string:
[H][C@@](COP([O-])(OCC[N+](C([2H])([2H])[2H])(C([2H])([2H])[2H])C([2H])([2H])[2H])=O)(OC(CCCCCCCCCCCCCCC)=O)COC(CCCCCCCCCCCCCCC)=O

Img

Sigma Aldrich

860353P

--


Assay:
>99% (TLC)

form:
powder

packaging:
pkg of 1 × 10 mg (860353P-10mg)

manufacturer/tradename:
Avanti Polar Lipids 860353P

shipped in:
dry ice

storage temp.:
−20°C

SMILES string:
[H][C@@](COP([O-])(OC([2H])([2H])C([2H])([2H])[N+](C([2H])([2H])[2H])(C([2H])([2H])[2H])C([2H])([2H])[2H])=O)(OC(CCCCCCCCCCCCCCC)=O)COC(CCCCCCCCCCCCCCC)=O