SORBITAN MONOPALMITATE
Relevant Data
Food Additives Approved in the United States
Food Additives Approved by European Union:
General Information
Chemical Names: | MIXTURE OF THE PARTIAL ESTERS OF SORBITOL AND ITS MONO- AND DIANHYDRIDES WITH EDIBLE PALMITIC ACID |
CAS number: | 26266-57-9 |
INS: | 495 |
Functional Class: |
Food Additives EMULSIFIER |
From apps.who.int
Evaluations
Evaluation year: | 1973 |
ADI: | 0-25 mg/kg bw |
Meeting: | 17 |
Specs Code: | R |
Comments: | Group ADI. As the sum of the sorbitan esters of lauric, oleic, palmitic and stearic acid |
Report: | NMRS 53/TRS 539-JECFA 17/21 |
Tox Monograph: | FAS 17-JECFA 26/218 (1982) |
Specification: | COMPENDIUM ADDENDUM 8/FNP 52 Add.8/203 (METALS LIMITS) (2000). R; FAO JECFA Monographs 1 vol.3/407 |
From apps.who.int
GSFA Provisions for SORBITAN MONOPALMITATE
Number | Food Category | Max Level | Notes |
---|---|---|---|
01.3.2 | Beverage whiteners |
4,000 mg/kg | Note XS252,Note XS250 |
07.1.4 | Bread-type products, including bread stuffing and bread crumbs |
10,000 mg/kg | Note 11 |
05.1.4 | Cocoa and chocolate products |
10,000 mg/kg | Note 101 |
05.1.1 | Cocoa mixes (powders) and cocoa mass/cake |
2,000 mg/kg | Note 97,Note 123,Note XS141 |
05.1.3 | Cocoa-based spreads, including fillings |
10,000 mg/kg | Note XS86 |
07.1.2 | Crackers, excluding sweet crackers |
10,000 mg/kg | Note 11 |
01.4.4 | Cream analogues |
5,000 mg/kg | Note 349 |
01.7 | Dairy-based desserts (e.g. pudding, fruit or flavoured yoghurt) |
5,000 mg/kg | Note XS243 |
06.4.2 | Dried pastas and noodles and like products |
5,000 mg/kg | Note 11,Note 211 |
04.2.2.2 | Dried vegetables (including mushrooms and fungi, roots and tubers, pulses and legumes, and aloe vera), seaweeds, and nuts and seeds |
5,000 mg/kg | Note 76 |
02.3 | Fat emulsions mainly of type oil-in-water, including mixed and/or flavoured products based on fat emulsions |
5,000 mg/kg | Note 363 |
02.2.2 | Fat spreads, dairy fat spreads and blended spreads |
10,000 mg/kg | Note 359 |
04.1.2.8 | Fruit preparations, including pulp, purees, fruit toppings and coconut milk |
5,000 mg/kg | Note XS240,Note XS314R |
01.5.2 | Milk and cream powder analogues |
4,000 mg/kg | Note XS251 |
07.1.6 | Mixes for bread and ordinary bakery wares |
10,000 mg/kg | Note 11 |
07.1.3 | Other ordinary bakery products (e.g. bagels, pita, English muffins) |
10,000 mg/kg | Note 11 |
06.4.3 | Pre-cooked pastas and noodles and like products |
5,000 mg/kg | Note 11,Note 194 |
05.2.2 | Soft candy |
10,000 mg/kg | Note XS309R |
07.1.5 | Steamed breads and buns |
10,000 mg/kg | Note 11 |
From www.fao.org
Computed Descriptors
Download SDF2D Structure | |
CID | 70687305 |
IUPAC Name | [2-[(2R,3R,4S)-3,4-dihydroxyoxolan-2-yl]-2-hydroxyethyl] hexadecanoate |
InChI | InChI=1S/C22H42O6/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-20(25)27-17-19(24)22-21(26)18(23)16-28-22/h18-19,21-24,26H,2-17H2,1H3/t18-,19?,21+,22+/m0/s1 |
InChI Key | IYFATESGLOUGBX-NDUCAMMLSA-N |
Canonical SMILES | CCCCCCCCCCCCCCCC(=O)OCC(C1C(C(CO1)O)O)O |
Molecular Formula | Â |
From Pubchem
Computed Properties
Property Name | Property Value |
---|---|
Molecular Weight | 402.572 |
Hydrogen Bond Donor Count | 3 |
Hydrogen Bond Acceptor Count | 6 |
Rotatable Bond Count | 18 |
Complexity | 389.0 |
CACTVS Substructure Key Fingerprint | A A A D c f B 4 O A A A A A A A A A A A A A A A A A A A A S A A A A A A A A A A A A A A A A A A A A A A G g A A C A A A C B S g g A I C C A A A B g A I A A C Q C A A A A A A A A A A A A A E A A A A B E B I A A A A C Q A A F A A A D A A H I 6 K y A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A = = |
Topological Polar Surface Area | 96.2 |
Monoisotopic Mass | 402.298 |
Exact Mass | 402.298 |
XLogP3 | None |
XLogP3-AA | 5.8 |
Compound Is Canonicalized | True |
Formal Charge | 0 |
Heavy Atom Count | 28 |
Defined Atom Stereocenter Count | 3 |
Undefined Atom Stereocenter Count | 1 |
Defined Bond Stereocenter Count | 0 |
Undefined Bond Stereocenter Count | 0 |
Isotope Atom Count | 0 |
Covalently-Bonded Unit Count | 1 |
From Pubchem
ADMET Predicted Profile --- Classification
Model | Result | Probability |
---|---|---|
Absorption | ||
Blood-Brain Barrier | BBB- | 0.5115 |
Human Intestinal Absorption | HIA+ | 0.7412 |
Caco-2 Permeability | Caco2- | 0.7155 |
P-glycoprotein Substrate | Substrate | 0.7152 |
P-glycoprotein Inhibitor | Non-inhibitor | 0.7597 |
Non-inhibitor | 0.7910 | |
Renal Organic Cation Transporter | Non-inhibitor | 0.8617 |
Distribution | ||
Subcellular localization | Mitochondria | 0.7318 |
Metabolism | ||
CYP450 2C9 Substrate | Non-substrate | 0.8343 |
CYP450 2D6 Substrate | Non-substrate | 0.8246 |
CYP450 3A4 Substrate | Non-substrate | 0.5152 |
CYP450 1A2 Inhibitor | Non-inhibitor | 0.7887 |
CYP450 2C9 Inhibitor | Non-inhibitor | 0.8702 |
CYP450 2D6 Inhibitor | Non-inhibitor | 0.9275 |
CYP450 2C19 Inhibitor | Non-inhibitor | 0.7688 |
CYP450 3A4 Inhibitor | Non-inhibitor | 0.8485 |
CYP Inhibitory Promiscuity | Low CYP Inhibitory Promiscuity | 0.9426 |
Excretion | ||
Toxicity | ||
Human Ether-a-go-go-Related Gene Inhibition | Weak inhibitor | 0.9504 |
Non-inhibitor | 0.5734 | |
AMES Toxicity | Non AMES toxic | 0.9257 |
Carcinogens | Non-carcinogens | 0.9509 |
Fish Toxicity | High FHMT | 0.9016 |
Tetrahymena Pyriformis Toxicity | High TPT | 0.9977 |
Honey Bee Toxicity | High HBT | 0.6743 |
Biodegradation | Ready biodegradable | 0.8186 |
Acute Oral Toxicity | IV | 0.6205 |
Carcinogenicity (Three-class) | Non-required | 0.7159 |
From admetSAR
ADMET Predicted Profile --- Regression
Model | Value | Unit |
---|---|---|
Absorption | ||
Aqueous solubility | -1.3754 | LogS |
Caco-2 Permeability | -0.1810 | LogPapp, cm/s |
Distribution | ||
Metabolism | ||
Excretion | ||
Toxicity | ||
Rat Acute Toxicity | 1.1117 | LD50, mol/kg |
Fish Toxicity | 2.0923 | pLC50, mg/L |
Tetrahymena Pyriformis Toxicity | 0.7120 | pIGC50, ug/L |
From admetSAR
Taxonomic Classification
Kingdom | Organic compounds |
---|---|
Superclass | Lipids and lipid-like molecules |
Class | Fatty Acyls |
Subclass | Fatty acid esters |
Intermediate Tree Nodes | Not available |
Direct Parent | Fatty acid esters |
Alternative Parents | |
Molecular Framework | Aliphatic heteromonocyclic compounds |
Substituents | Fatty acid ester - Oxolane - Carboxylic acid ester - Secondary alcohol - Carboxylic acid derivative - Dialkyl ether - Ether - Monocarboxylic acid or derivatives - Oxacycle - Organoheterocyclic compound - Carbonyl group - Organic oxide - Alcohol - Organooxygen compound - Hydrocarbon derivative - Organic oxygen compound - Aliphatic heteromonocyclic compound |
Description | This compound belongs to the class of organic compounds known as fatty acid esters. These are carboxylic ester derivatives of a fatty acid. |
From ClassyFire