Articles:
benzeneacetic acid, a-hydroxy-
Notes:
It is an isomer of cresotinic acid (2-hydroxy-3-methylbenzoic acid) and oxymethylbenzoic acid (2-methoxybenzoic acid). Derivatives of mandelic acid are formed as a result of metabolism of adrenaline and noradrenaline by monoamine oxidase and catechol-o-methyl transferase. It is also present in certain skin care products, is an intermediate molecule in the production of other biochemicals, may be used as an analytical reagent and is a precursor in the manufacture of dyes.
Mandelic acid is an aromatic alpha hydroxy acid with the molecular formula C8H8O3. It is a white crystalline solid that is soluble in water and most common organic solvents. [HMDB]
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American International Chemical, Inc. Consistent sources North American supplier for globally sourced ingredients. AIC is a Westborough, MA based ISO Certified sales and marketing company serving the food, pharmaceutical, nutritional, personal care, biotech, and industrial markets of North America since 1972. Our success is a result of a company culture built on customer needs, along with partnerships with global manufacturers committed to the rigors and demands of the North American market. Our team of Sales Representatives, along with our network of strategically located warehouses are ready to supply product when and where you need it. Email: Info Voice: (800) 238-0001 Facebook Twitter Linkedin Products List: View Product(s): 113602 Mandelic Acid
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BOC Sciences Best of Chemicals Supplier Quality supplier of research chemicals and biochemicals including inhibitors, building blocks, GMP Products, impurities and metabolites, APIs for Veterinary, Natural Compounds, ADCs, Stem Cell Molecule and chiral compounds. BOC Sciences provides a wide range of services to support the pharmaceutical industry through all stages of drug discovery including Custom Synthesis of those chemicals that are not in stock, Isotope Labeling Service, Chiral Synthesis and Resolution, Bioconjugation, PEGylation services, analytical services. BOC Sciences is a brand of BOCSCI Inc. We leverage our wide spectrum of business in the fields of development, manufacturing, marketing, and distribution to help you make best-informed decisions tailored to your evolving needs for premium chemicals. Our complete suite of CRO services spans the entire molecule development pipeline including contract research for target identification, building blocks, compound synthesis, biochemical and cellular analysis, preclinical animal tests, and clinical studies. Email: Marketing US Email: Marketing Email: Sales US Email: Sales Voice: 1-631-485-4226 Fax: 1-631-614-7828 US Voice: 1-631-485-4226 US Fax: 1-631-614-7828 Europe 44-203-286-1088 Facebook Twitter Linkedin Blog Get the App! Product(s): 90-64-2 DL-Mandelic acid Mandelic acid was first discovered while heating amygdalin isolated from bitte
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Jiangyin Healthway International Trade Co., Ltd Independent Ingredients Supplier We provide custom synthesis and contract manufacturing from milligrams to metric tonnes. Jiangyin Healthway International Trade Co., Ltd is a professional company, main engaged in manufacturing and exporting aroma chemicals ,food additives , cosmetic ingredient ,pharmaceutical intermediates & other fine chemicals; especially on aroma chemicals , as the major manufacturer of heterocyclic and sulphur aroma compounds , we are the leading independent ingredients supplier to the flavour and fragrance industries in China, can offer hundreds of different high quality aroma chemicals. Email: Info Email: Sales Voice: 86-510-86023169 Fax: 86-510-86023170 Mobile 0086-13093133011 Services Biochemical Natural Food Colour New functional food ingredients Product(s): HLC-306 Mandelic Acid HLCFD-133 Mandelic Acid
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Penta International Corporation Chemistry innovation At Penta, our products and services help businesses do business better. For over 30 years, Penta Manufacturing Company has played a growing role in worldwide chemistry innovations and applications. As an industry leader, Penta continues to pioneer chemistry-based solutions for practically every area of commerce. Our products and expertise have helped fuel technical advances in dozens of commercial applications including flavoring, coloring, fragrances and chemical processes. US Email: Technical Services US Email: Sales US Voice: (973) 740-2300 US Fax: (973) 740-1839 Product(s): 13-05805 MANDELIC ACID NF
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TCI AMERICA Moving Your Chemistry Forward We continuously strive to advance our technology. With East & West Coast distribution centers, count on TCI to deliver products quickly and reliably. Over 30,000 Reagents available today in benchtop to bulk quantities. We also offer custom synthesis solutions. Sign up for a TCI account today for fast and free shipping! Tokyo Chemical Industry Co., Ltd. (TCI) is a leading worldwide manufacturer of specialty organic chemicals founded in 1946. TCI provides organic laboratory chemicals as well as pharmaceutical, cosmetic and functional materials. More than 70 years of synthesis experience and multi-purpose plants enable TCI to offer more than 30,000 products as well as custom synthesis. US Email: Sales Email: Technical Support Voice: 1-800-423-8616 Fax: 1- 888-520-1075 Facebook Twitter Instagram Linkedin Product(s): M0038 DL-Mandelic Acid >99.0%(GC)(T)
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| CAS Number: | 90-64-2 |  3D/inchi
|
| Other(deleted CASRN): | 15769-78-5 | |
| ECHA EINECS - REACH Pre-Reg: | 202-007-6 | |
| FDA UNII: | NH496X0UJX | |
| Nikkaji Web: | J3.918G | |
| Beilstein Number: | 510011 | |
| MDL: | MFCD00064250 | |
| XlogP3: | 0.60 (est) | |
| Molecular Weight: | 152.14936000 | |
| Formula: | C8 H8 O3 | |
| BioActivity Summary: | listing | |
| NMR Predictor: | Predict (works with chrome or firefox) | |
Category: antimicrobial agents
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 |
Physical Properties:
| Assay: | 95.00 to 100.00 % |
| Food Chemicals Codex Listed: | No |
| Melting Point: | 119.00 °C. @ 760.00 mm Hg |
| Boiling Point: | 321.83 °C. @ 760.00 mm Hg (est) |
| Flash Point: | 325.00 °F. TCC ( 162.60 °C. ) (est) |
| logP (o/w): | 0.620 |
| Soluble in: | |
| water, 1.81E+05 mg/L @ 25 °C (exp) | |
| water, 1.763e+005 mg/L @ 25 °C (est) | |
Organoleptic Properties:
| Odor and/or flavor descriptions from others (if found). | |
Cosmetic Information:
| CosIng: | cosmetic data |
| Cosmetic Uses: |
antimicrobial agents |
Suppliers:
| Alfa Biotechnology |
| For experimental / research use only. |
| DL-Mandelic acid 98% |
| American International Chemical, LLC. |
| Mandelic Acid |
| BOC Sciences |
| For experimental / research use only. |
| DL-Mandelic acid
Odor: characteristic Use: Mandelic acid was first discovered while heating amygdalin isolated from bitte |
| Indis NV |
| For experimental / research use only. |
| (±)-Mandelic Acid |
| Jiangyin Healthway |
| Mandelic Acid |
| New functional food ingredients |
| Jiangyin Healthway |
| Mandelic Acid |
| M.C.Biotec |
| Mandelic Acid
Odor: characteristic Use: useful in suppressing pigmentation, treating inflammatory noncystic acne, and rejuvenating photoaged skin. Moreover it has proven useful in preparing the skin for laser peeling and in helping the skin heal after laser surgery. |
| Penta International |
| MANDELIC ACID NF |
| Santa Cruz Biotechnology |
| For experimental / research use only. |
| DL-Mandelic acid |
| Sigma-Aldrich: Aldrich |
| For experimental / research use only. |
| Mandelic acid 99% |
| Spec-Chem Industry |
| SpecWhite ® DL-MA |
| TCI AMERICA |
| For experimental / research use only. |
| DL-Mandelic Acid >99.0%(GC)(T) |
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: | |
|
oral-rabbit LDLo 2000 mg/kg GASTROINTESTINAL: GASTRITIS LIVER: OTHER CHANGES GASTROINTESTINAL: ULCERATION OR BLEEDING FROM STOMACH Archives Internationales de Pharmacodynamie et de Therapie. Vol. 64, Pg. 79, 1940. intramuscular-rat LD50 > 300 mg/kg Experimental Medicine and Surgery. Vol. 4, Pg. 223, 1946. intraperitoneal-rat LD50 4100 mg/kg Bollettino Chimico Farmaceutico. Vol. 112, Pg. 53, 1973. oral-rat LDLo 3000 mg/kg Archives Internationales de Pharmacodynamie et de Therapie. Vol. 64, Pg. 79, 1940. | |
| Dermal Toxicity: | |
| Not determined | |
| Inhalation Toxicity: | |
| Not determined | |
Safety in Use Information:
| Category: | antimicrobial agents | ||
| Recommendation for (±)-mandelic acid usage levels up to: | |||
| not for fragrance use. | |||
| Recommendation for (±)-mandelic acid flavor usage levels up to: | |||
| not for flavor use. | |||
Safety References:
| EPI System: | View |
| AIDS Citations: | Search |
| Cancer Citations: | Search |
| Toxicology Citations: | Search |
| EPA Substance Registry Services (TSCA): | 90-64-2 |
| EPA ACToR: | Toxicology Data |
| EPA Substance Registry Services (SRS): | Registry |
| Laboratory Chemical Safety Summary : | 1292 |
| National Institute of Allergy and Infectious Diseases: | Data |
| WGK Germany: | 3 |
| 2-hydroxy-2-phenylacetic acid | |
| Chemidplus: | 0000090642 |
| RTECS: | OO6300000 for cas# 90-64-2 |
References:
| 2-hydroxy-2-phenylacetic acid | |
| NIST Chemistry WebBook: | Search Inchi |
| Canada Domestic Sub. List: | 90-64-2 |
| Pubchem (cid): | 1292 |
| Pubchem (sid): | 134971115 |
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 |
| KEGG (GenomeNet): | C01984 |
| HMDB (The Human Metabolome Database): | HMDB00703 |
| FooDB: | FDB022191 |
| Export Tariff Code: | 2918.19.1200 |
| ChemSpider: | View |
| Wikipedia: | View |
Potential Blenders and core components note
| None Found | ||
Potential Uses:
| None Found |
Occurrence (nature, food, other): note
| not found in nature |
Synonyms:
| almond acid | |
| amygdalic acid | |
| amygdalinic acid | |
| benzeneacetic acid, a-hydroxy- | |
| glycolic acid, phenyl- | |
| 2- | HPAA |
| (2RS)-2- | hydroxy-2-phenylacetic acid |
| 2- | hydroxy-2-phenylacetic acid |
| DL-2- | hydroxy-2-phenylacetic acid |
| (±)-2- | hydroxy-2-phenylethanoic acid |
| 2- | hydroxy-2-phenylethanoic acid |
| a- | hydroxy-a-toluic acid |
| hydroxy-phenyl-acetic acid | |
| hydroxy(phenyl)acetic acid | |
| DL- | hydroxy(phenyl)acetic acid |
| (±)-a- | hydroxybenzeneacetic acid |
| a- | hydroxybenzeneacetic acid |
| (±)-a- | hydroxyphenylacetic acid |
| a- | hydroxyphenylacetic acid |
| mandelic acid | |
| (RS)- | mandelic acid |
| DL- | mandelic acid |
| racemic | mandelic acid |
| DL- | mandelicacid |
| paramandelic acid | |
| 2- | phenyl-2-hydroxyacetic acid |
| phenylglycolic acid | |
| 2- | phenylglycolic acid |
| DL- | phenylglycolic acid |
| phenylhydroxyacetic acid | |
| a- | toluic acid, a-hydroxy- |
| uromaline |