EU/US Properties Organoleptics Cosmetics Suppliers Safety Safety in use Safety references References Other Blenders Uses Occurrence Synonyms Articles Notes
 

acetyl glutamic acid
N-acetyl glutamate

Supplier Sponsors

CAS Number: 1188-37-0Picture of molecule3D/inchi
Other(deleted CASRN):7728-87-2
ECHA EINECS - REACH Pre-Reg:214-708-4
FDA UNII: MA61H539YZ
Nikkaji Web:J37.497K
Beilstein Number:1727473
MDL:MFCD00002802
XlogP3:-1.80 (est)
Molecular Weight:189.16767000
Formula:C7 H11 N O5
BioActivity Summary:listing
NMR Predictor:Predict (works with chrome, Edge or firefox)
EFSA/JECFA Comments:
mp: 199-201°; Optical rotation: -25.6° (22 °C in water)
Category:flavor enhancers, umami taste enhancer
 
US / EU / FDA / JECFA / FEMA / FLAVIS / Scholar / Patent Information:
Google Scholar:Search
Google Books:Search
Google Scholar: with word "volatile"Search
Google Scholar: with word "flavor"Search
Google Scholar: with word "odor"Search
Google Patents:Search
US Patents:Search
EU Patents:Search
Pubchem Patents:Search
PubMed:Search
NCBI:Search
JECFA Food Flavoring:2269 N-acetyl glutamate
FEMA Number:4752 N-acetyl glutamate
FDA:No longer provide for the use of these seven synthetic flavoring substances
 
Physical Properties:
Appearance:white powder (est)
Assay: 95.00 to 100.00
Food Chemicals Codex Listed: No
Melting Point: 199.00 to 201.00 °C. @ 760.00 mm Hg
Boiling Point: 495.00 to 496.00 °C. @ 760.00 mm Hg
Flash Point: 488.00 °F. TCC ( 253.33 °C. )
logP (o/w): -2.131 (est)
Soluble in:
 water, 8.524e+005 mg/L @ 25 °C (est)
 
Organoleptic Properties:
Odor and/or flavor descriptions from others (if found).
 
Cosmetic Information:
CosIng:cosmetic data
Cosmetic Uses: skin conditioning
 
Suppliers:
BOC Sciences
For experimental / research use only.
N-Acetyl-L-Glutamic acid 95%
Carbosynth
For experimental / research use only.
N-Acetyl-L-glutamic acid
Glentham Life Sciences
N-Acetyl-L-glutamic acid
Penta International
N-ACETYL-L-GLUTAMIC ACID
Santa Cruz Biotechnology
For experimental / research use only.
N-Acetyl-L-glutamic acid
Sigma-Aldrich: Aldrich
For experimental / research use only.
N-Acetyl-L-glutamic acid, ReagentPlus®, 99%
TCI AMERICA
For experimental / research use only.
N-Acetyl-L-glutamic Acid >98.0%(HPLC)(T)
United International
N-Acetyl-L-glutamic acid
United International
N-Acetyl-L-Glutamine Nat.
 
Safety Information:
Preferred SDS: View
 
Hazards identification
 
Classification of the substance or mixture
GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)
None found.
GHS Label elements, including precautionary statements
 
Pictogram
 
Hazard statement(s)
None found.
Precautionary statement(s)
None found.
Oral/Parenteral Toxicity:
intraperitoneal-mouse LD50 711 mg/kg
BEHAVIORAL: CONVULSIONS OR EFFECT ON SEIZURE THRESHOLD BEHAVIORAL: SOMNOLENCE (GENERAL DEPRESSED ACTIVITY) LUNGS, THORAX, OR RESPIRATION: DYSPNEA
Toksikologicheskii Vestnik. Vol. (3), Pg. 36, 1995.

oral-mouse LD50 6838 mg/kg
BRAIN AND COVERINGS: "CHANGES IN CIRCULATION (HEMORRHAGE, THROMBOSIS, ETC.)" LUNGS, THORAX, OR RESPIRATION: OTHER CHANGES BLOOD: HEMORRHAGE
Toksikologicheskii Vestnik. Vol. (3), Pg. 36, 1995.

oral-rat LD50 > 7000 mg/kg
LUNGS, THORAX, OR RESPIRATION: OTHER CHANGES BRAIN AND COVERINGS: "CHANGES IN CIRCULATION (HEMORRHAGE, THROMBOSIS, ETC.)" BLOOD: HEMORRHAGE
Toksikologicheskii Vestnik. Vol. (3), Pg. 36, 1995.

Dermal Toxicity:
Not determined
Inhalation Toxicity:
Not determined
 
Safety in Use Information:
Category:
flavor enhancers, umami taste enhancer
Recommendation for acetyl glutamic acid usage levels up to:
 not for fragrance use.
 
Use levels for FEMA GRAS flavoring substances on which the FEMA Expert Panel based its judgments that the substances are generally recognized as safe (GRAS).
The Expert Panel also publishes separate extensive reviews of scientific information on all FEMA GRAS flavoring substances and can be found at FEMA Flavor Ingredient Library
publication number: 26
Click here to view publication 26
 average usual ppmaverage maximum ppm
baked goods: --
beverages(nonalcoholic): 50.00000150.00000
beverages(alcoholic): --
breakfast cereal: --
cheese: 50.00000150.00000
chewing gum: --
condiments / relishes: 20.00000100.00000
confectionery froastings: --
egg products: --
fats / oils: 25.00000100.00000
fish products: 50.00000150.00000
frozen dairy: --
fruit ices: --
gelatins / puddings: --
granulated sugar: --
gravies: 50.00000150.00000
hard candy: --
imitation dairy: 50.00000150.00000
instant coffee / tea: 50.00000150.00000
jams / jellies: --
meat products: 50.00000150.00000
milk products: 50.00000200.00000
nut products: --
other grains: --
poultry: 50.00000150.00000
processed fruits: --
processed vegetables: 25.00000100.00000
reconstituted vegetables: 25.00000100.00000
seasonings / flavors: 50.00000500.00000
snack foods: 50.00000200.00000
soft candy: --
soups: 50.00000150.00000
sugar substitutes: --
sweet sauces: 50.00000150.00000
 
Safety References:
EPI System: View
AIDS Citations:Search
Cancer Citations:Search
Toxicology Citations:Search
EPA Substance Registry Services (TSCA):1188-37-0
EPA ACToR:Toxicology Data
EPA Substance Registry Services (SRS):Registry
Laboratory Chemical Safety Summary :70914
National Institute of Allergy and Infectious Diseases:Data
WGK Germany:2
(2S)-2-acetamidopentanedioic acid
Chemidplus:0001188370
RTECS:LZ9725000 for cas# 1188-37-0
 
References:
 (2S)-2-acetamidopentanedioic acid
NIST Chemistry WebBook:Search Inchi
Pubchem (cid):70914
Pubchem (sid):135028765
 
Other Information:
(IUPAC):Atomic Weights of the Elements 2011 (pdf)
Videos:The Periodic Table of Videos
tgsc:Atomic Weights use for this web site
(IUPAC):Periodic Table of the Elements
CHEBI:View
CHEMBL:View
Golm Metabolome Database:Search
Metabolomics Database:Search
KEGG (GenomeNet):C00624
HMDB (The Human Metabolome Database):HMDB01138
FooDB:FDB022447
YMDB (Yeast Metabolome Database):YMDB00066
Export Tariff Code:2924.19.1150
ChemSpider:View
Wikipedia:View
 
Potential Blenders and core components note
None Found
 
Potential Uses:
 additives
 skin conditioning
 
Occurrence (nature, food, other):note
 not found in nature
 
Synonyms:
(2S)-2-acetamidopentanedioic acid
N-acetyl glutamate
N-acetyl-L-glutamic acid
N-acetyl-laevo-glutamic acid
L-acetylglutamic acid
L-glutamic acid, N-acetyl-
laevo-glutamic acid, N-acetyl-
 
 
Notes:
N-Acetylglutamic acid (abbreviated NAcGlu) is biosynthesized from glutamic acid and acetyl-CoA by the enzyme NAGS. The reverse reaction, hydrolysis of the acetyl group, is catalyzed by a specific hydrolase. [HMDB]
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