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N-Cyclohexylsulphamic acid sodium salt

Sodium cyclamate

CAS: 139-05-9;68476-78-8

Molecular Formula: C6H14NNaO3S

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N-Cyclohexylsulphamic acid sodium salt - Names and Identifiers

Name Sodium cyclamate
Synonyms asugryn
cyclamic
Beet molasses
Sodium cyclamate
Cyclamate Sodium
assurgrinvollsuss
assurgrinfeinsuss
Beet Sugar Molasses
cyclamate,sodiumsalt
sodium cyclohexylsulfamate
sodium cyclohexylsulphamate
sodium cyclohexanesulfamate
Sodium N-cyclohexylsulfamate
cyclamic acid sodium crystalline
Cyclohexansulfamic acid Sodium salt
cyclohexyl-sulfamicacimonosodiumsalt
cyclohexylsulfamic acid, sodium salt
N-Cyclohexylsulphamic acid sodium salt
cyclohexanesulfamicacid,monosodiumsalt
cyclohexanesulphamicacid,monosodiumsalt
Sodium cyclamate~Sodium N-cyclohexylsulphamate
CAS 139-05-9
68476-78-8
EINECS 205-348-9
InChI InChI=1/C6H13NO3S.Na/c8-11(9,10)7-6-4-2-1-3-5-6;/h6-7H,1-5H2,(H,8,9,10);/q;+1/p-1
InChIKey UDIPTWFVPPPURJ-UHFFFAOYSA-M

N-Cyclohexylsulphamic acid sodium salt - Physico-chemical Properties

Molecular FormulaC6H14NNaO3S
Molar Mass203.23
Density1.58[at 20℃]
Melting Point>300 °C (lit.)
Water Solubility>=10 g/100 mL at 20 ºC
Solubility Soluble in water (1g/5ml) propylene glycol (1g/25ml), almost insoluble in ethanol, ether, benzene and chloroform.
Vapor Presure0.002Pa at 150℃
AppearanceWhite crystalline powder
ColorWhite
Merck14,2703
BRN4166868
PH5.5-7.5 (100g/l, H2O, 20℃)
Storage Conditionroom temp
SensitiveSensitive to light
MDLMFCD00003827
Physical and Chemical PropertiesWhite crystalline powder, odorless, sweetness of sucrose 40~50 times. Soluble in water (1g/5mL), slightly soluble in propylene glycol (1g/25mL), insoluble in ethanol, chloroform, benzene and ether. The pH value of 10% aqueous solution was 6.5. No moisture absorption, alkali resistance, heat resistance (decomposition temperature 28 degrees C), light resistance. Mouse oral LD5018000mg/kg,Adl 0~11 mg/kg(FAO/WHO,1994).
UseUsed as food processing sweeteners, drugs, cosmetics, feed additives

N-Cyclohexylsulphamic acid sodium salt - Risk and Safety

Hazard SymbolsXn - Harmful
Harmful
Risk Codes22 - Harmful if swallowed
Safety DescriptionS36/37 - Wear suitable protective clothing and gloves.
S24/25 - Avoid contact with skin and eyes.
WGK Germany3
RTECSGV7350000
TSCAYes
HS Code29299000
ToxicitySodium cyclamate is a non-nutritive sweetener
that is about 30 times sweeter than cane sugar. The oral LD50s
in rats and mice are 15.25 and 17.0 g/kg, respectively. It was
banned as a food additive because of findings that it caused
bladder cancer in rodents. It appears to act as a promoter.
There is also evidence that it causes toxicity in the male reproductive
system.

N-Cyclohexylsulphamic acid sodium salt - Upstream Downstream Industry

Raw MaterialsSulfamic acid
Cyclohexylamine

N-Cyclohexylsulphamic acid sodium salt - Reference

Reference
Show more
1. Huang Zhuoquan, Liu Huan, Mai Runqiu, et al. Exposure Risk Assessment of Four Food Additives for Bergamot Cold Fruit [J]. Journal of Food Safety and Quality Inspection 2020 011(008):2645-2649.
2. Shi Yan, Zhao Shanshan, Ji Ningning, et al. Fiber Quality Analysis of Dissolving Pulp Cellulose Fiber in NaOH/Additive Aqueous Solution [J]. Polymer Bulletin, 2016(12):43-49.
3. Xiao Xiaoyi, Xia Yanbin, Yuan He, et al. Ultrasonic Extraction/Gas Chromatography for Detection of Sodium Cyclamate in Edible Areca Nut [J]. Agricultural Products Processing, 2019(14).
4. Bingxue Hu, Da-Wen Sun, Hongbin Pu, Qingyi Wei, A dynamically optical and highly stable pNIPAM @ Au NRs nanohybrid substrate for sensitive SERS detection of malachite green in fish fillet, talanta, Volume 218, 2020, 121188, ISSN 0039-9140, https://doi.org/

N-Cyclohexylsulphamic acid sodium salt - Nature

Open Data Verified Data

white crystalline powder, odorless, 40 to 50 times the sweetness of sucrose, soluble in water (lg/5mL), slightly soluble in propylene glycol (1g/25mL), insoluble in ethanol, chloroform, benzene and ether. The pH value of 10% aqueous solution was 6.5. Stable to heat, light and air, stable under alkaline conditions, slightly decomposed when acidic. No hygroscopicity.

Last Update:2024-01-02 23:10:35

N-Cyclohexylsulphamic acid sodium salt - Preparation Method

Open Data Verified Data

obtained by the reaction of cyclohexylamine and sodium aminosulfonate through crystallization and purification. Alternatively, it is prepared by the reaction of cyclohexylamine and sulfur trioxide. It can also be obtained from the reaction of cyclohexylamine and chlorosulfonic acid.

Last Update:2022-01-01 10:10:06

N-Cyclohexylsulphamic acid sodium salt - Standard

Authoritative Data Verified Data

This product is cyclohexanesulfonic acid sodium salt. Calculated as the dried product, the content of CsH 12nna03s F is less than 98.0%.

Last Update:2024-01-02 23:10:35

N-Cyclohexylsulphamic acid sodium salt - Trait

Authoritative Data Verified Data
  • This product is white crystalline powder; Odorless, sweet.
  • This product is soluble in water, very slightly soluble in ethanol, insoluble in chloroform or ether.
Last Update:2022-01-01 11:23:05

N-Cyclohexylsulphamic acid sodium salt - Introduction

The decomposition temperature is about 280 ℃, no caramelization reaction occurs, and the pH of the 10% aqueous solution is 5-5-7-5. Stable to heat, light, air, stable under alkaline, slightly decomposed when acidic. Sweet, slightly bitter when heated.
Last Update:2022-10-16 17:13:46

N-Cyclohexylsulphamic acid sodium salt - Use

Open Data Verified Data

sodium cyclamate is a commonly used non-nutritive sweetener. In the human body is not absorbed, does not produce heat. Taste close to sucrose, often mixed with saccharin sodium, can mask the bitter taste of saccharin sodium. For pickles, sauces, wine, cakes, biscuits, bread, ice cream, ice cream
The maximum usage amount is 0. 65g/kg; The maximum usage amount of candied fruit is 1.0g/kg; The maximum usage amount of tangerine peel, plum and dried Bayberry is 8. Og/kg.

Last Update:2022-01-01 10:10:07

N-Cyclohexylsulphamic acid sodium salt - Differential diagnosis

Authoritative Data Verified Data
  1. take this product about O. lg, add 10ml water to dissolve, add hydrochloric acid lm l and barium chloride solution (l - 1 0) lm l, the solution should be clear; Add sodium nitrite solution (1-1 0) lm l, A white precipitate was produced.
  2. The infrared absorption spectrum of this product should be consistent with that of the reference product (General rule 0402).
  3. identification reaction of sodium salt of this product (General rule 0301).
Last Update:2022-01-01 11:23:06

N-Cyclohexylsulphamic acid sodium salt - Exam

Authoritative Data Verified Data

absorbance

take this product l .O g, add water 10ml to dissolve, according to UV-visible spectrophotometry (General rule 0401), at the wavelength of 270mn absorbance, should not exceed 0.10.


pH

This product l .O g, add water 10ml to dissolve, according to the law (General 0631),p H value should be 5. 5~7. 5.


clarity and color of solution

The pH value of the solution shall be checked according to law (General rule 0901 and General Rule 0 9 0 2) and shall be clear and colorless.


sulfate

take this product 0. 50g, check according to law (General rule 0802), compared with the standard potassium sulfate solution 1 .2m l made of the control solution, not more concentrated (0.024%).


cyclohexylamine

take 1 0g of this product, weigh it accurately, put it in a 100ml measuring flask, add water to dissolve and dilute it to the scale, shake it well, and use it as a test solution. lg, precision weighing, put in a 100ml measuring flask, quickly add 50ml of hydrochloric acid solution (1 -100) to dissolve, dilute with water to the scale, shake, take appropriate amount of precision measurement, A solution containing 2.5 of cyclohexylamine per l of 1 m of Phine was prepared by dilution with water as a control solution. The sample solution and the reference solution were respectively placed in 60ml separatory funnel, and alkaline ethylenediamine tetraacetic acid disodium solution (10g of ethylenediamine tetraacetic acid disodium and sodium hydroxide 3) was added. 4G, add water to dissolve and dilute to 100ml and shake to obtain) 15.0 mL and m l of trimethyl methane-n-butanol (20: 1), shake for 2 minutes, and let stand, separate the three-gas methane layer, accurately measure 10 M l, put it in another separatory funnel, add methyl orange boric acid solution (take methyl orange 200mg and Na 3 .5G, add 100ml of water, heat on the water bath to dissolve, stand still for more than 24 hours, immediately before filtering to take the filtrate, that is, 2.0), shake for 2 minutes, stand still, separate the chloroform layer, add anhydrous sodium sulfate (l g), shake and let stand; Take 5ml of the three-gas methane solution precisely, put it in a colorimetric tube, and add methanol-sulfuric acid (50: 1)0. 5 m l, shake well, the color of the test solution should not be deeper than the reference solution; Or according to UV-visible spectrophotometry (General rule 0401), determine the absorbance at the wavelength of 520nm, the absorbance of the test solution should not be greater than the absorbance of the control solution (0. 00 25%).


loss on drying

take this product, dry to constant weight at 105°C, weight loss shall not exceed 1.0% (General rule 0831).


precious metals

take l .O g of this product, add 23ml of water to dissolve, add 2ml of acetate buffer (pH3.5), and check according to law (the first method of general rule 0821), containing heavy metals not more than 10 parts per million.


arsenic salt

Take 2. O g of this product, add 0822 of water to dissolve, add 5ml of hydrochloric acid, and check according to law (General rule 0.0001% first law), shall comply with the provisions ().

Last Update:2022-01-01 11:23:07

N-Cyclohexylsulphamic acid sodium salt - Content determination

Authoritative Data Verified Data

take this product about 0. 16G, precision weighing, add glacial acetic acid 40 m l, dissolve at a slight temperature, let cool, add 2 drops of crystal violet indicator solution, and use perchloric acid titration solution (0. lm o l/L) titration to the solution is green and the results of the titration are corrected with a blank test. Each lm l perchloric acid titration solution (0. lm o l/L) corresponds to 20. 12mg of C6H 12 NNa03S.

Last Update:2022-01-01 11:23:07

N-Cyclohexylsulphamic acid sodium salt - Category

Authoritative Data Verified Data

pharmaceutical excipients, sweeteners and flavoring agents.

Last Update:2022-01-01 11:23:08

N-Cyclohexylsulphamic acid sodium salt - Storage

Authoritative Data Verified Data

sealed storage.

Last Update:2022-01-01 11:23:08

N-Cyclohexylsulphamic acid sodium salt - Reference Information

LogP-2.63 at 20℃
(IARC) carcinogen classification 3 (Vol. Sup 7, 73) 1999
EPA chemical information Information provided by: ofmpub.epa.gov (external link)
identification test soluble in water, almost insoluble in ethanol. Measured according to OT-42 method. Add 1ml of hydrochloric acid to 10ml of 1% sample solution, mix, and add 1ml of barium chloride test solution (TS-37). The obtained solution should still be clear, such as adding 1ml of sodium nitrite test solution (TS-226). There are white precipitates. Positive for sodium test (IT-28).
content analysis after the sample is pre-dried at 105 ℃ for 1 hour, about 0.4g is accurately weighed, dissolved in a mixed solution prepared from 50ml of water and 5ml of dilute hydrochloric acid test solution (TS-117), and titrated with 0.1mol/L sodium nitrite solution. When titrating to the last 1ml of titration solution, it should be added drop by drop, and the end point should be immediately blue when the glass rod stained with iodine starch test paper is extended into the titrated solution, or the end point should be determined by potentiometric titration. When the titration is complete, the above endpoint phenomenon can still be reproduced after being maintained by drops for 1min. 0.1mol/L sodium nitrite solution per ml is equivalent to 20.12mg of sodium cyclohexylsulfamate (C6H12N3NaOS).
toxicity ADI value 0~11 mg/kg (calculated as cyclohexylsulfamic acid; FAO/WHO,2001). LD5015250mg/kg (rats, oral); Rats were fed with 1.0% for 2 years without any abnormality. For the human body, after oral administration, 40% is excreted by urine and 60% excreted by stool. According to U.S. regulations (FDA 189.135,2000), this product is still prohibited from being directly added or used in food.
usage limit GB 2760-2002(g/kg): pickles, sauces, prepared wine, cakes, biscuits, bread, ice cream, ice cream, popsicles, beverages, jelly, 0.65; Candied fruit, 1.0; melon seeds, 2.0; dried tangerine peel, plum, plum, dried bayberry, 8.0.
Use Used as a sweetener for food processing, an additive for medicines, cosmetics, and feed
The sweetness of this product is about 30 times that of sucrose. Dilute 1:10000 (sucrose 1:140, saccharin 1:50000) can still feel sweet. As a non-nutritional sweetener, it is used in all aspects. The concentration should not exceed 0.4% to ease the bitterness. According to China's GB2760-86 regulations, it can be used for cool drinks, ice cream, cakes and candied fruits. In addition, according to the supplementary provisions of the GB2760-89, it can also be used as additives for pickles, seasoning sauce, prepared wine, cakes, biscuits, complexion, etc.
Sodium cyclamate is a commonly used non-nutritional synthetic sweetener. It is not absorbed in the human body, does not generate heat, and does not cause caries. The taste is close to sucrose and is often mixed with sodium saccharin (10:1) to mask the bitter taste of sodium saccharin. It can be used for tangerine peel, plum, dried bayberry and plum, with a maximum usage of 8.0 g/kg; The maximum usage in candied fruit is 1.0 g/kg; The maximum usage is 0.65 g/kg in pickles, sauces, prepared wine, beverages, popsicles, ice cream, ice cream, cakes, biscuits and bread.
No nutrient sweetener. It can be used in all aspects, mainly for diabetic patients. The concentration should not exceed 0.4% to ease the bitterness.
Production method After sulfonating cyclohexylamine with chlorosulfonic acid or sulfamate to cyclohexylsulfamic acid, it is neutralized and refined with sodium hydroxide.
Synthesis of Cyclohexylamine and Sulfur Trioxide This is the production method of Baldwin-Montrose Chemical Company in the United States. (CH3)3N SO3 →(CH3)3NSO3[C6H11NH2] →[NaOH] → C6H11NHSO3Na Dissolve trimethylamine and sulfur trioxide in tetrachloroethylene solvent respectively, and then mix and react to form a suspension of trimethylamine-sulfur trioxide complex. This suspension is then added to an aqueous solution of cyclohexylamine and sodium hydroxide, and reacted at 60~70°C to form sodium cyclohexanesulfonate. 40g of liquid SO3 can also be dissolved in 200 mLCH2C12, added dropwise to 150mL of solution dissolved with 56g of triethylamine at-I0 ℃, and reacted at a constant temperature for 15min to generate triethylamine sulfur trioxide complex. The equimolar cyclohexylamine was added dropwise at 20 ℃ for 1h. After the reaction was complete, NaOH solution of 250mL 10% was added and reacted at 60 ℃ for 1h. The product is obtained by concentration, cooling, crystallization, suction filtration and drying of the separated water layer, and the yield is about 95%. In addition, Japan's Nido Chemical Company adopts the process route of gas phase reaction of sulfur trioxide and cyclohexylamine. Cyclohexylamine and sulfamic acid (or salt) synthesis method Japan Jifu Pharmaceutical Co., Ltd. uses cyclohexylamine and sodium sulfamate as raw materials to produce cyclamate. The reaction is carried out in a light oil solvent at 180~200 ℃. After the reaction, it is crystallized and recrystallized to obtain the finished product, and the mother liquor is returned to the reactor for reuse. This method is easy to obtain raw materials, simple operation, easy recovery of solvent and high yield. Domestic research on the optimization of the process conditions reported that 25g of cyclohexylamine was added dropwise to a mixture of 10g of sulfamic acid and 35g of light oil, reacted at 165 ℃ for 3h, then cooled to below 130 ℃, 41g of 10% sodium bicarbonate solution was added to dissolve the product, then distilled to recover light oil and cyclohexylamine, and finally the crude product was recrystallized with 97.5% yield. C6H11NH2 + NH2SO3Na → C6H11NHSO3Na + NH3 ↑ Japan Toyo Chemical Co., Ltd. uses cyclohexylamine and sulfamic acid as raw materials to produce cyclamate at 160~179 ℃ and o-dichlorobenzene. The second reaction temperature is controlled below 130 ℃. The unreacted cyclohexylamine and o-dichlorobenzene are steamed out with steam and reused. The reactants are crystallized and recrystallized to obtain the finished product. The raw materials of this method are cheap and easy to obtain, the solvent is easy to recover, the reaction time is short, and the yield is high. 2CaH11NH2 + NH2SO3H → C6H11NHSO3NH3C6H11[NaOH] → Synthesis of C6H11NHSO3Na Cyclohexylamine and Chlorosulfonic Acid This is the production method of a Japanese company. 2C6H11NH2 + ClSO3H[<5 ℃ = → C6H11NHSO3NH3C6H11[NaOH] → C6H11NHSO3Na reaction After separation, concentration and extraction, 95% finished products are obtained. The method has cheap raw materials and fast reaction, but has more side reactions and serious equipment corrosion.
Using cyclohexylamine as raw material, sulfonated with chlorosulfonic acid or sulfamate to cyclohexylsulfamic acid and then reacted with sodium hydroxide.
Last Update:2024-04-09 02:00:06
N-Cyclohexylsulphamic acid sodium salt
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View History
N-Cyclohexylsulphamic acid sodium salt
DGTP, NA2H2
METHYLENEDIOXYCINNAMOYLPEPERIDINE
Disodium hydrogen phosphate anhydrous
金黃大茴香酸
2-吡咯烷酮-5-羧酸镁
苯甲酰基亚胺酸乙酯盐酸盐
2-甲基-3-氨基-5-氯苯甲酸甲酯
(2-Amino-tert-butyl)carbamic acid tert-butyl ester monohydrochloride
Bis(2-propenyl) trisulfide
Raw Materials for N-Cyclohexylsulphamic acid sodium salt
Sulfamic acid
Cyclohexylamine
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