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

para-anthranilic acid
benzoic acid, 4-amino-

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Name:4-aminobenzoic acid
CAS Number: 150-13-0Picture of molecule3D/inchi
Other(deleted CASRN):8014-65-1
ECHA EINECS - REACH Pre-Reg:205-753-0
FDA UNII: TL2TJE8QTX
Nikkaji Web:J5.852A
Beilstein Number:0471605
MDL:MFCD00007894
XlogP3:0.80 (est)
Molecular Weight:137.13819000
Formula:C7 H7 N O2
BioActivity Summary:listing
NMR Predictor:Predict (works with chrome, Edge or firefox)
Category:miscellaneous
 
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
Perfumer and Flavorist:Search
Google Patents:Search
US Patents:Search
EU Patents:Search
Pubchem Patents:Search
PubMed:Search
NCBI:Search
FDA Mainterm (SATF):150-13-0 ; P-AMINOBENZOIC ACID
 
Physical Properties:
Assay: 95.00 to 100.00
Food Chemicals Codex Listed: No
Specific Gravity:1.37400 @ 25.00 °C.
Melting Point: 188.00 to 189.00 °C. @ 760.00 mm Hg
Boiling Point: 339.00 to 340.00 °C. @ 760.00 mm Hg (est)
Flash Point: 319.00 °F. TCC ( 159.40 °C. ) (est)
logP (o/w): 0.830
Soluble in:
 alcohol
 water, 6110 mg/L @ 30 °C (exp)
 
Organoleptic Properties:
Odor and/or flavor descriptions from others (if found).
 
Cosmetic Information:
CosIng:cosmetic data2
CosIng:cosmetic data
Cosmetic Uses: not used anymore
 
Suppliers:
AIDP
PABA Para amino benzoic acid, 4-Aminobenzoic acid 98.5%-101.5%
American International Chemical, LLC.
PABA
BOC Sciences
For experimental / research use only.
Tetracaine HCl Impurity A 95%
Odor: characteristic
Use: 4-Aminobenzoic Acid, also called as PABA, was used as sunscreening agent at the past due to its UV absorption and antifibrotic properties.
Charkit Chemical
AMINOBENZOIC ACID, P-
EMD Millipore
For experimental / research use only.
4-Aminobenzoic acid
Glentham Life Sciences
4-Aminobenzoic acid, USP grade
Glentham Life Sciences
4-Aminobenzoic acid
Indis NV
For experimental / research use only.
PABA (Para Amino Benzoic Acid)
Penta International
P-AMINOBENZOIC ACID USP
Santa Cruz Biotechnology
For experimental / research use only.
p-Aminobenzoic acid 99%
Sigma-Aldrich: Aldrich
For experimental / research use only.
p-Aminobenzoic acid ReagentPlus®, 99%
TCI AMERICA
For experimental / research use only.
4-Aminobenzoic Acid >99.0%(HPLC)(T)
 
Safety Information:
Preferred SDS: View
European information :
Most important hazard(s):
Xi - Irritant
R 36/37/38 - Irritating to eyes, respiratory system, and skin.
R 43 - May cause sensitisation by skin contact.
S 02 - Keep out of the reach of children.
S 24/25 - Avoid contact with skin and eyes.
S 26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S 37/39 - Wear suitable gloves and eye/face protection.
 
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:
oral-rat LD50 > 6000 mg/kg
Proceedings of the Society for Experimental Biology and Medicine. Vol. 49, Pg. 184, 1942.

intraperitoneal-rat LD50 > 3450 mg/kg
Bollettino Chimico Farmaceutico. Vol. 112, Pg. 53, 1973.

oral-rabbit LD50 1830 mg/kg
Bollettino Chimico Farmaceutico. Vol. 112, Pg. 53, 1973.

intravenous-rabbit LD50 2000 mg/kg
Federation Proceedings, Federation of American Societies for Experimental Biology. Vol. 1, Pg. 71, 1942.

oral-mouse LD50 2850 mg/kg
BEHAVIORAL: MUSCLE WEAKNESS BEHAVIORAL: SOMNOLENCE (GENERAL DEPRESSED ACTIVITY)
Proceedings of the Society for Experimental Biology and Medicine. Vol. 49, Pg. 184, 1942.

oral-dog LD50 1000 mg/kg
Proceedings of the Society for Experimental Biology and Medicine. Vol. 49, Pg. 184, 1942.

oral-rabbit LD50 1830 mg/kg
Federation Proceedings, Federation of American Societies for Experimental Biology. Vol. 10, Pg. 289, 1951.

Dermal Toxicity:
Not determined
Inhalation Toxicity:
Not determined
 
Safety in Use Information:
Category:
miscellaneous
Recommendation for para-anthranilic acid usage levels up to:
 not for fragrance use.
 
Recommendation for para-anthranilic acid flavor usage levels up to:
 not for flavor use.
 
Safety References:
EPI System: View
Chemical Carcinogenesis Research Information System:Search
AIDS Citations:Search
Cancer Citations:Search
Toxicology Citations:Search
EPA Substance Registry Services (TSCA):150-13-0
EPA ACToR:Toxicology Data
EPA Substance Registry Services (SRS):Registry
Laboratory Chemical Safety Summary :978
National Institute of Allergy and Infectious Diseases:Data
WGK Germany:2
4-aminobenzoic acid
Chemidplus:0000150130
EPA/NOAA CAMEO:hazardous materials
RTECS:DG1400000 for cas# 150-13-0
 
References:
 4-aminobenzoic acid
NIST Chemistry WebBook:Search Inchi
Canada Domestic Sub. List:150-13-0
Pubchem (cid):978
Pubchem (sid):134973070
 
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
FDA Substances Added to Food (formerly EAFUS):View
CHEBI:View
CHEMBL:View
Golm Metabolome Database:Search
Metabolomics Database:Search
UM BBD:Search
KEGG (GenomeNet):C00568
HMDB (The Human Metabolome Database):HMDB01392
FooDB:FDB001037
YMDB (Yeast Metabolome Database):YMDB00493
Export Tariff Code:2922.49.1000
FDA Listing of Food Additive Status:View
ChemSpider:View
Wikipedia:View
Formulations/Preparations:
sunscreens are available in a variety of dosage forms and formulations. ? because these formulations frequently change and the manufacturers often are reluctant to reveal specific ingredients in their formulations, a listing of commercially available sunscreens is not included in this monograph. technical, national formulary capsules and tablets (as the potassium salt), 500 mg; packets (as the potassium salt) 2 g; powder topical cream, aminobenzoic acid 4% and titanium dioxide 12%, solar spf 15 (spf 15), doak; lipstick, aminobenzoic acid 5% and red pertolatum, rvpaba (spf 10), elder; lotion, aminobenzoic acid 5%, oxybenzone 3%, and padimate o 5%, presun 15 sunscreen lotion (with sd alcohol 40 58%; spf 15), westwood-squibb.
 
Potential Blenders and core components note
None Found
 
Potential Uses:
 u.v. absorbers
 
Occurrence (nature, food, other):note
 not found in nature
 pineapple fruit
Search Trop Picture
 rice plant
Search Trop Picture
 
Synonyms:
 ABEE
 actipol
4-amino benzoic acid
p-amino benzoic acid
1-amino-4-carboxybenzene
p-amino-benzoic acid
4-aminobenzoic acid
gamma-aminobenzoic acid
p-aminobenzoic acid
para-aminobenzoic acid
4-aminobenzoicacid
 aniline-4-carboxylic acid
p-anthranilic acid
 anti-gray-hair factor
 anticantic vitamin
 antichromotrichia factor
 benzoic acid, 4-amino-
4-carboxyaniline
p-carboxyaniline
para-carboxyaniline
p-carboxyphenyl amine
para-carboxyphenyl amine
4-carboxyphenylamine
 PABA
 trochromogenic factor
 
 
Notes:
A member of the VITAMIN B COMPLEX. It used to be common in SUNSCREENING AGENTS until found to also be a sensitizer. The potassium salt is used therapeutically in fibrotic skin disorders. a member of the vitamin b complex. it used to be common in sunscreening agents until found to also be a sensitizer. the potassium salt is used therapeutically in fibrotic skin disorders. Listed in the EAFUS Food Additive Database (Jan. 2001) but with no reported use 4-Aminobenzoic acid (also known as para-aminobenzoic acid or PABA) is an organic compound with the molecular formula C7H7NO2. PABA is a white crystalline substance that is only slightly soluble in water. It consists of a benzene ring substituted with an amino group and a carboxyl group.; 4-Aminobenzoic acid, para-aminobenzoic acid, or simply PABA, is an organic compound with molecular formula C7H7NO2. PABA is a white crystalline substance that is only slightly soluble in water. It consists of a benzene ring substituted with an amino group and a carboxylic acid.; A member of the vitamin B complex. It used to be a common sunscreening agent until found to also be a sensitizer. The potassium salt is used therapeutically in fibrotic skin disorders.; PABA is an essential nutrient for some bacteria and is sometimes called Vitamin Bx. However, PABA is not essential for humans and it varies in its activity from other B vitamins. Although humans lack the ability to synthesize folate from PABA, it is sometimes marketed as an essential nutrient under the premise that it can stimulate intestinal bacteria.; PABA is an essential nutrient for some bacteria and is sometimes called Vitamin Bx. In humans, PABA is normally made by E. coli in the colon and therefore PABA from food is not normally essential to human health. PABA is therefore not officially classified as a vitamin. PABA is an intermediate in bacterial synthesis of folate. Although humans lack the ability to synthesize folate from PABA, that is also normally done by E. coli. PABA is sometimes marketed as an essential nutrient for use whenever normal PABA synthesis by intestinal bacteria is insufficient.
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