Trolamine Salicylate

HCID 25213

Basic information

CAS
2174-16-5
Standard SMILES
O=C(O)c1ccccc1O.OCCN(CCO)CCO
InChIKey
UEVAMYPIMMOEFW-UHFFFAOYSA-N
Molecular formula
C13H21NO6
Average molar mass
287.31 g/mol
Monoisotopic mass
287.13688739

Names & identifiers

Preferred name
Trolamine Salicylate
IUPAC
2-[bis(2-hydroxyethyl)amino]ethanol;2-hydroxybenzoic acid
English name
Triethanolamine salicylate
Molecular formula
C13H21NO6
Molecular weight
287.31

Names & synonyms

TROLAMINE SALICYLATETriethanolamine salicylate2174-16-5TEA-SalicylateTEA salicylateNeo heliopan tsNeotan wArthricreamDTXSID4047969H8O4040BHDTrolamine salicylate (USP)DTXCID4027945
Show more names
Triethanolaminium salicylateTriethanolamine salicylate,99%Salicylic acid·triethanolamineSalicylicacidtriethanolaminesaltTrolamine salicylate in methanoltea-salicylate,triethanolaminesalicylateSalicylic acid·2,2',2''-nitrilotrisethanol
Trolamine salicylate [USP]CannaflexHempvanaArthritis CreamArthritis LeaderArthritis ReliefAsper-FlexAsper-Flex Cream

Database identifiers

CAS
2174-16-5
PubChem CID
25213
DTXSID
DTXSID4047969
ChEMBL
CHEMBL2107288
UNII
H8O4040BHD
EC Number
218-531-3

Properties

Computed structural properties

Topological polar surface area
121 Ų
Hydrogen bond donors
5
Hydrogen bond acceptors
7
Rotatable bonds
7
Heavy atoms
20

Experimental & physicochemical properties

SolubilitySoluble
Boiling PointDecomposes
Melting Point50

Physicochemical properties

Density
1.209 g/mL · 1.209 g/mL at 25 °C
refractive index
20 · n20/D 1.509
Flash point
113 °C · 113 °C
Odor
dull pleasent sweet
BRN
7451205 · 7451205
Cosmetics Ingredients Functions
PRESERVATIVEUV FILTERLIGHT STABILIZER

Safety & regulation

GHS classification

GHS Classification · 5 items

Warning

H302 (97.6%): Harmful if swallowed [Warning Acute toxicity, oral];H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation];H319 (100%): Causes serious eye irritation [Warning Serious eye damage/eye irritation];H335 (100%): May cause respiratory irritation [Warning Specific target organ toxicity, single exposure; Respiratory tract irritation]

P261, P264, P264+P265, P270, P271, P280, P301+P317, P302+P352, P304+P340, P305+P351+P338, P319, P321, P330, P332+P317, P337+P317, P362+P364, P403+P233, P405, and P501 (click each P-code to see the statement)

Aggregated GHS information provided per 42 reports by companies from 3 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.;Information may vary between notifications depending on impurities, additives, and other factors. The percentage value in parenthesis indicates the notified classification ratio from companies that provide hazard codes. Only hazard codes with percentage values above 10% are shown. For more detailed information, please visit ECHA C&L website.

Hazard information

Regulatory InformationChemical: Benzoic acid, 2-hydroxy-, compound with 2,2',2''-nitrilotris[ethanol] (1:1)
Other Safety InformationIMAP assessments - Benzoic acid, 2-hydroxy-, compound with 2,2',2''-nitrilotris[ethanol] (1:1): Human health tier I assessment
Hazard Classes and CategoriesAcute Tox. 4 (97.6%);Skin Irrit. 2 (100%);Eye Irrit. 2 (100%);STOT SE 3 (100%)

Toxicology

Toxicity Summary · 2 items

The Panel concluded that the following ingredients are safe in cosmetics in the present practices of use and concentration described in the safety assessment, when formulated to be non-irritating and non-sensitizing, which may be based on a quantitative risk assessment (QRA)...TEA-Salicylate...

Safe for use in cosmetics, with qualifications

Regulatory information

Regulatory InformationChemical: Benzoic acid, 2-hydroxy-, compound with 2,2',2''-nitrilotris[ethanol] (1:1)

Safety data

wgk
3
tsca
TSCA listed
hs_code
29225000
risk_code
20/21/22-36/37/38-22
Signal word
Warning
Symbol(GHS)
GHS07

Chemistry & industry

Pharmacology

Pharmacodynamics · 1 item

Trolamine salicylate is a salicylate that inhibits cyclo-oxygenase (COX) enzymes responsible for generating pro-inflammatory factors such as to induce pain and inflammation. It is thought to mediate its analgesic effect through inhibition of COX-2 enzyme, which is an induced enzyme responsible for inflammatory responses and pain in muscle and joint disorders. By inhibiting fatty acid COX enzyme, trolamine salicylate inhibits the production of prostaglandins and thromboxanes in inflammatory cells involved in generating pain and inflammation. It thereby works to temporarily reduce mild to moderate pain. In subjects with muscle soreness from exercise, administration of topical trolamine salicylate was associated with reduced duration and severity of muscule soreness compared to placebo. In subjects with osteoarthritis in hands, trolamine salicylate cream was shown to be effective in achieving temporary relief of minor pain and stiffness.

Mechanism of Action · 1 item

Inflammation and tissue damage in different conditions including arthritis, bursitis, joint disorder, bruises, and strains or sprains of muscle origin, induce mild to moderate pain and are associated with increase prostaglandin synthesis. This is thought to be a result of COX-2 enzyme induction. COX-2 is induced in inflammatory cells in case of cell injury, infection or activation from inflammatory cytokines such as interleukin (IL)-1 and tumor necrosis factor (TNF)-α. Upon activation, COX-2 produces prostanoid mediators of inflammation such as prostaglandins and thromboxanes. Trolamine salicylate mediates its analgesic effect by inhibiting the production of inflammatory mediators that sensitize nociceptive nerve endings and generate pain.

Absorption, Distribution and Excretion · 3 items

Following topical administration of 10% trolamine salicylate in healthy volunteers, salicylic acid could not be detected in serum indicating low systemic absorption.

Following topical administration of 10% trolamine salicylate in healthy volunteers, urinary recovery of total salicylate during the first 24 hours was 6.9 mg (p < 0.05), which is 1.4% of total dose.

Topical administration of 1 gram of 10% trolamine salicylate in abdominal rat skin resulted in an approximate extravascular volume of distribution (V/F) of 24.0 mL.

Uses & manufacturing

UsesCIR ingredient: TEA-Salicylate
Household ProductsInformation on 1 consumer products that contain TEA-salicylate in the following categories is provided:;• Personal Care
Use ClassificationCosmetics -> Preservative
General Manufacturing InformationBenzoic acid, 2-hydroxy-, compd. with 2,2',2''-nitrilotris[ethanol] (1:1): ACTIVE
Applications · 2 items

UsesTEA-salicylate is a chemical uVB absorber. This is one of the 21 FDAapproved sunscreen chemicals with an approved usage level of 5 to 12 percent. TeA-salicylate is a water-soluble chemical with limited uV absorption capability. Formulators may also use it as a preservative.

UsesTriethanolaMine salicylate can be used as intermediate in the manufacture of surface active agents, textile specialties, waxes, polishes, herbicides, petroleum demulsifiers, toilet goods, cement additives, cutting oils. In making emulsions with mineral and vegetable oils, paraffin and waxes. Solvent for casein, shellac, dyes; manufacture of synthetic resins; increasing the penetration of organic liquids into wood and paper. In the production of lubricants for the textile industry. Pharmaceutic aid (alkalizer).

Upstream & downstream products

Upstream raw materials

Suppliers36 total

北京华美互利生物化工010-56205725 · [email protected]
湖北万得化工有限公司15377098680 15377098680 · [email protected]
Hebei Zhuanglai Chemical Trading Co Ltd+86-16264648883 · [email protected]
杭州品高化工有限公司0571-87658025 · [email protected]
普善实业(陕西)有限公司029-81310890 18165209495 · [email protected]

Related reactions

1 records

Compound notes

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