Boswellia serrata

CAS 631-69-6C30H48O3MW 456.7

Boswellia serrata (CAS 631-69-6) — formula C30H48O3, molecular weight 456.7; category food flavors.

Product Overview

CAS Number	631-69-6
Molecular Formula	C30H48O3
Molecular Weight	456.7
LogP	8.3
Category	Flavors & Fragrances

Technical Profile

What this product is

Boswellia serrata is a flavoring compound with CAS registry number 631-69-6 and molecular formula C30H48O3 (molecular weight 456.7), belonging to the food flavors segment of chemical raw materials.

Identification

CAS number: 631-69-6

Its molecular formula C30H48O3 comprises 30 C, 48 H, 3 O atoms.

Also known as: Boswellia serrata · beta-boswellic acid · Boswellic Acid

Category: food flavors

Frequently Asked Questions

What is the CAS number of Boswellia serrata?

The CAS registry number of Boswellia serrata is 631-69-6.

What is the molecular formula and molecular weight of Boswellia serrata?

Molecular formula C30H48O3, molecular weight 456.7.

What other names is Boswellia serrata known by?

It is also registered under: Boswellia serrata, beta-boswellic acid, Boswellic Acid.

Which category does Boswellia serrata belong to?

Category: Flavors & Fragrances.

PubChem Public Data

Independent reference data for Boswellia serrata (CAS 631-69-6), compiled from public chemistry databases.

Registry identifiers across databases

CAS Registry Number	631-69-6
PubChem CID	168928
Molecular formula	C30H48O3
IUPAC name	(3R,4R,4aR,6aR,6bS,8aR,11R,12S,12aR,14aR,14bR)-3-hydroxy-4,6a,6b,8a,11,12,14b-heptamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picene-4-carboxylic acid
UNII (FDA)	B252M1YO2V

Computed descriptors

Molecular Weight	456.7
XLogP3	8.3
Hydrogen Bond Donor Count	2
Hydrogen Bond Acceptor Count	3
Rotatable Bond Count	1
Exact Mass	456.36034539
Monoisotopic Mass	456.36034539
Topological Polar Surface Area	57.5
Heavy Atom Count	33

Documented uses on record

Anti-inflammatory agents that are non-steroidal in nature. In addition to anti-inflammatory actions, they have analgesic, antipyretic, and platelet-inhibitory actions. They act by blocking the synthesis of prostaglandins by inhibiting cyclooxygenase, which converts arachidonic acid to cyclic endoperoxides, precursors of prostaglandins. Inhibition of prostaglandin synthesis accounts for their analgesic, antipyretic, and platelet-inhibitory actions; other mechanisms may contribute to their anti-inflammatory effects.

Synonyms and trade names

beta-Boswellic acid; 631-69-6; Boswellic acid; B252M1YO2V; DTXSID2057578; (4R)-3alpha-Hydroxyurs-12-en-24-oic acid; Urs-12-en-23-oic acid, 3-hydroxy-, (3alpha,4beta)-; 12-Ursene-3,24-diol; RefChem:119215; DTXCID2020428; b-Boswellic acid; CHEMBL267225; ss-Boswellic Acid; UNII-B252M1YO2V; NBGQZFQREPIKMG-PONOSELZSA-N; yena-Boswellic acid

What the public record says

Boswellic Acid · CAS 631-69-6 · C30H48O3. UNII B252M1YO2V.

Physical description and handling notes

Source: PubChem / Wikidata; the batch COA governs where values differ.

Boswellia serrata

Product Overview

Technical Profile

What this product is

Identification

Frequently Asked Questions

PubChem Public Data

Registry identifiers across databases

Computed descriptors

Documented uses on record

Synonyms and trade names

What the public record says

Physical description and handling notes

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