ivy carbaldehyde / methyl anthranilate schiff's base

vertosine (Symrise)

CAS: 68738-99-8 C17 H21 N O2 MW: 271.35977000 green

Identification

Nameivy carbaldehyde / methyl anthranilate schiff's base
IUPACmethyl 2-[[(E)-(2,4-dimethyl-1-cyclohex-3-enylidene)methyl]amino]benzoate
CAS Number68738-99-8
EINECS272-124-5
FDA UNIISearch
Molecular FormulaC17 H21 N O2
Molecular Weight271.35977000

Regulatory

Physical Properties

Appearance yellow solid (est)
Assay 94.00 to 100.00 sum of isomers
Food Chemicals Codex Listed No
Specific Gravity 1.08300 to 1.09100 @ 25.00 °C.
Pounds per Gallon - (est). 9.012 to 9.078
Refractive Index 1.59900 to 1.60500 @ 20.00 °C.
Boiling Point 401.00 to 405.00 °C. @ 760.00 mm Hg, 405.00 to 406.00 °C. @ 760.00 mm Hg (est)
Flash Point 291.00 °F. TCC ( 143.89 °C. )
logP (o/w) 5.856 (est)
Soluble in alcohol
Insoluble in water
Stability ph from 12.2

Cosmetic Information

CosIngcosmetic data
Cosmetic Usesperfuming agents

Organoleptic Properties

Odor Strength medium ,
Substantivity 400 hour(s) at 100.00 %
Odor Description
at 10.00 % in dipropylene glycol.
intense green, floral-aldehydic, reminiscent of the green note of broom (genet)
A fresh green, sweet floral note with orange flower characteristics
floreal, herbaceous, citrusy, lemon and mandarin note
GREEN, FLORAL, ALDEHYDIC, CITRUS
Odor sample from Harrmann & Reimer Corporation

Safety Information

European informationMost important hazard(s):
Human ExperienceNo effects detrimental to health are known.
Oral/Parenteral Toxicityoral-rat LD50 > 5000 mg/kg
Dermal ToxicityNot determined
Inhalation ToxicityNot determined

GHS Classification

['GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)', 'GHS Label elements, including precautionary statements']

Safety in Use

Categoryfragrance agents
RIFM Fragrance Material Safety AssessmentSearch
IFRA Critical EffectSensitization
fragrance material specificationThe IFRA Scientific Committee examined the physicochemical properties of Schiff bases and concluded that, based on the available information, these materials should be considered under contributions from other sources. By default, the stoichiometric presence of the aldehydes of the Schiff bases is taken into account assuming 100% dissociation. An indicative list of Schiff bases incorporating aldehydes covered by an IFRA Standard of restriction is reported at
Recommendation for ivy carbaldehyde / methyl anthranilate schiff's base usage levels up to4.0000 % in the fragrance concentrate.
Recommendation for ivy carbaldehyde / methyl anthranilate schiff's base flavor usage levels up tonot for flavor use.

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Potential Uses

FR balsam FR citrus fir FR fresh and clean FR gardenia FR genet FR green FR herbal FR honeysuckle FR jasmin leaf FR lily FR linden flower FR mimosa FR narcissus natural FR orange blossom peel FR pine FR tuberose

Natural Occurrence

not found in nature

Synonyms

agrumea (iff) benzoic acid, 2-(((2,4(or 3,5)-dimethyl-3-cyclohexen-1-yl)methylene)amino)-, methyl ester 2-(((2,4(3,5)- dimethyl-3-cyclohexen-1-yl)methylene)amino) methyl benzoate ivy carbaldehyde / methyl anthranilate schiff's base ligantraal (Quest) methyl 2-((-1-(2,4-dimethyl-3-cyclohexenyl)methylidene)amino)-1-benzene carboxylate methyl 2-(((2,4(or 3,5)-dimethyl-3-cyclohexen-1-yl)methylene)amino) benzoate methyl 2-(((2,4(or 3,5)-dimethyl-3-cyclohexen-1-yl)methylene)amino)benzoate methyl 2-(((2,4(or 3,5)-dimethyl-3-cyclohexenyl)methylene)amino) benzoate methyl 2-[[(E)-(2,4-dimethyl-1-cyclohex-3-enylidene)methyl]amino]benzoate methyl anthranilate / ivy carbaldehyde schiff's base methyl anthranilate / 2,4(or 3,5)-dimethyl-3-cyclohexene-1-carboxaldehyde methyl dimethyl cyclohexenyl methylene aminobenzoate methyl-(3,5-dimethyl-3-cyclohexene-1-yl) methylene anthranilate vertosine (Symrise) Try the PubMed Search.